Substituted 6-(1h-pyrazol-1-yl)pyrimidin-4-amine derivatives and uses thereof

ABSTRACT

The present invention covers substituted 6-(1H-pyrazol-1-yl)pyrimidin-4-amine compounds of general formula (I) as described and defined herein, methods of preparing said compounds, intermediate compounds useful for preparing said compounds, pharmaceutical compositions and combinations comprising said compounds, and the use of said compounds for manufacturing pharmaceutical compositions for the treatment or prophylaxis of diseases, in particular for the treatment and/or prophylaxis of cardiovascular and renal diseases, as a sole agent or in combination with other active ingredients.

The present invention covers substituted6-(1H-pyrazol-1-yl)pyrimidin-4-amine compounds of general formula (I) asdescribed and defined herein, methods of preparing said compounds,intermediate compounds useful for preparing said compounds,pharmaceutical compositions and combinations comprising said compounds,and the use of said compounds for manufacturing pharmaceuticalcompositions for the treatment or prophylaxis of diseases, in particularfor the treatment and/or prophylaxis of cardiovascular and renaldiseases, as a sole agent or in combination with other activeingredients.

BACKGROUND

Vascular calcification is one of the major life-threating complicationsin patients with chronic kidney disease (CKD) (Neven at al Calcif TissueInt (2016), 99:525-534). With CKD progression renal function declines,so called uremic toxins are retained and as consequence plasma levels ofinorganic phosphate (Pi) and other plasma components are subsequentlyincreased.

This is the origin of hyperphosphatemia which per se has been identifiedas an independent risk factor being responsible for further rapiddecline of kidney function. A large body of evidence directly linkshyperphosphatemia with adverse renal and cardiovascular outcomes. Inaddition patients with CKD are known to develop Pi imbalance and theuprgulation of phosphaturic hormones regulating renal phosphateexcretion like FGF23. FGF23 can be detected early on in the plasma ofCKD patients. Elevated FGF23 levels are associated with an increasedcardiovascular risk in CKD patients (Isakova JAMA 2011). Thereforecontrolling phosphate metabolism in patients with chronic kidney diseasehas been a major therapeutic challenge for nephrologists for decades(Evenepoel P. Kidney International 2016, 21-23).

The current treatment of hyperphosphatemia is summarized in the KidneyDisease improving global outcome (KDIGO)-CKD-Mineral and Bone Disorders(MBD) guidelines. The choice of the phosphate binder used is recommendedto be individualized for each patient considering the CKD stage,presents or absence of other components of CKD-mineral and bonedisorders, concomitant therapies and side-effect profile of each drug.Currently available phosphate binders can be roughly divided indifferent subclasses. Aluminium hydroxide and calcium based binders(CBB) like calcium acetate and calcium carbonate represent the firstgeneration of phosphate binders. However, their adverse effects likebone and central nervous system toxicity for aluminium hydroxide andhypercalcemia in up to 50% of the patient using CBBs, respectively,limited the use of these types of phosphate binders. Non-calcium basedbinders (NCBBs) like e.g. sevelamer hydrochloride and sevelamercarbonate, Lanthanum and lanthanum carbonate and magnesium based bindersare commonly used to treat hyperphosphatemia. Also combinations of lowdose CBBs and NCBBs, new phosphate binding agents like colestilan,iron-containing phosphate binders, inhibitors of the intestinal andrenal proximal tubule sodium-phosphate co-transporter like niacin ornicotinamide or other inhibitors like tenapanor (NHE3 inhibitor) areused to treat hyperphosphatemia (Spasovski Expert Opinion 2015,2589-2599).

Recently, a large body of in vivo and in vitro studies has shown thatfibroblast growth factor-23 (FGF23) in addtition to calcitriol,calcidiol, parathyroid hormone (PTH) is a key regulator of phosphatehomeostasis and therefore might be a good target to addresshyperphosphatemia (Gattineni Am J Physiol Renal Physiol 2009,F282-F291).

Although hyperphosphatemia is characterized by high plasma levels ofinorganic phosphate (Pi), inorganic phosphate is fundamental to cellularfunction and skeletal mineralization. Normal Pi intake in the adulthuman is in the range of 800 to 1600 mg/day. Approximately 65% to 75% ofingested Pi is absorbed in the small intestine, regardless of the levelof Pi intake, and hormonal regulation of this process plays only a minorrole in normal Pi homeostasis. Most of the absorbed Pi is excreted inthe urine. This means that Pi homeostasis and plasma Pi concentrationdepend primarily on renal mechanisms that regulate tubular Pi transport.(Tenenhouse H. S. Annu. Rev. Nutr. 2005, 240-247)

In general, members of two families of SLC proteins (SLC20 and SLC34)act as Na⁺-dependent, secondary-active co-transporters to transport Piacross cell membranes. The SLC34 proteins are expressed in specificorgans important for Pi homeostasis: NaPi-IIa (SLC34A1) and NaPi-IIc(SLC34A3) fulfill essential roles in Pi reabsorption in the kidneyproximal tubule and NaPi-IIb (SLC34A2) mediates Pi absorption in thegut. The SLC20 proteins, PiT-1 (SLC20A1), PiT-2 (SLC20A2) are expressedubiquitously in all tissues and although generally considered as“housekeeping” transport proteins, the discovery of tissue-specificactivity, regulatory pathways and gene-related pathophysiologies, isredefining their importance (Foster et al. Molecular Aspects of Medicine2013,386-395)

Npt2a was identified as the most prominent Pi transporter within thekidney and thereby being involved in the regulation of the Pi excretion(Biber et al Annu. Rev. Physiol. 2013, 535-550). Therefore Np2tainhibitors may have the potential to address cardiovascular(CV)-mortality and CV-morbidity by altering vascular calcification andplasma phosphate levels.

Npt2a inhibitors provide a novel approach to address vascularcalcification in patients with chronic kidney disease and/or in patientswith arterial hypertension, cardiac hypertrophy, ischemic heart disease,peripheral arterial disease and retinopathy.

Compounds that are inhibitors of the intestinal sodium-dependentphosphate transport Npt2b are described in WO2012/006473, inWO2012/006474, in WO2012/006477, in WO2012/054110, in WO2013/062065, inEP1465638, in EP1815860, in U.S. Pat. No. 6,355,823, in WO2016/082751and in WO2013/082756.

Substituted Pyrimidines are disclosed e.g. in U.S. Pat. No. 9,163,017 B2for the treatment of Hepatitis C, in WO2014152716 A1 for the treatmentand prevention of viral infections, in EP1841760B1 as kinase modulatorsfor the treatment of cancer and in WO2014181287A1 to treat inflammatorydiseases, autoimmune disorders and other related disorders.

However, the state of the art does not describe the6-(1H-pyrazol-1-yl)pyrimidin-4-amine compounds of general formula (I) ofthe present invention as described and defined herein.

It has now been found, and this constitutes the basis of the presentinvention, that the compounds of the present invention have surprisingand advantageous properties.

In particular, the compounds of the present invention have surprisinglybeen found to effectively reduce plasma phosphate levels and increaseurinary Pi excretion due to their Npt2a inhibition potential. Moreoverthe compounds of the present invention have surprisingly been found toeffectively inhibit vascular calcification and to reduce FGF-23 andparathyroid hormone levels significantly by inhibiting Npt2a and maytherefore be used for the treatment or prophylaxis of diseases and/orconditions associated with hyperphosphatemia, patients with disbalancedphosphate homeostasis, elevated plasma FGF23 levels, chronic kidneydisease (CKD), chronic kidney disease associated calcification,non-chronic kidney disease associated calcification, mediacalcifications including Moenckeberg's medial sclerosis,atherosclerosis, intima calcification, CKD associated heart hypertrophy,CKD associated renal dystrophy, osteoporosis, post-menopausalosteoporosis, diabetes mellitus II, chronic renal disease, aging,hypophosphaturia, hyperparathyroidism, Vitamin D disorders, Vitamin Kdeficiency, Vitamin K-antagonist coagulants, Kawasaki disease, ACDC(arterial calcification due to deficiency of CD73), GACI (generalizedarterial calcification of infancy), IBGC (idiopathic basal gangliacalcification), PXE (pseudoxanthoma elasticum), rheumatoid arthritis,Singleton-Merten syndrome, P-thalassemia, calciphylaxis, heterotrophicossification, preterm placental calcification, calcification of theuterus, calcified uterine fibroids, morbus fahr, mircocalcification andcalcification of the aortic valve.

DESCRIPTION OF THE INVENTION

The invention provides compounds of the formula

in which

-   R¹ represents a group of the formula

-   -   in which    -   # represents the point of attachment to the amino group,    -   R⁵ represents a group selected from a halogen atom, cyano,        (C₁-C₄)-alkyl, (C₁-C₄)-alkoxy, (C₃-C₆)-cycloalkyl, 4- to        6-membered heterocycle and (C₁-C₄)-alkylcarbonyl,        -   wherein said (C₁-C₄)-alkyl is optionally substituted,            identically or differently, with one or two groups selected            from —NR¹⁴R¹⁵, (C₁-C₄)-alkoxy and cyclopropyl and optionally            up to five fluorine atoms,            -   wherein said cyclopropyl is optionally substituted with                up to four fluorine atoms,            -   wherein            -   R¹⁴ represents a hydrogen atom or (C₁-C₄)-alkyl,            -   R¹⁵ represents a hydrogen atom or (C₁-C₄)-alkyl,            -   or            -   R¹⁴ and R¹⁵ together with the nitrogen atom they are                attached form a 4- to 5-membered heterocycle                -   wherein said 4- to 5-membered heterocycle is                    optionally substituted, identically or differently,                    with one, two or three groups selected from                    (C₁-C₄)-alkyl trifluormethyl, difluoromethyl and                    optionally up to five fluorine atoms,        -   wherein said (C₁-C₄)-alkoxy is optionally substituted with            up to three fluorine atoms,        -   wherein said 4- to 6-membered heterocycle is optionally            substituted, identically or differently, with one or two            groups selected from (C₁-C₄)-alkyl and optionally up to five            fluorine atoms,        -   wherein said (C₃-C₆)-cycloalkyl is optionally substituted,            identically or differently, with one or two groups selected            from (C₁-C₄)-alkyl and optionally up to five fluorine atoms,    -   R⁶ represents 6-membered heteroaryl, 2-oxopyridin-1(2H)-yl, a 4-        to 8-membered heterocycle or (C₄-C₈)-cycloalkyl,        -   or        -   represents a group of the formula

-   -   -   in which        -   ## represents the point of attachment to the pyrazole ring,        -   R³⁸ represents a hydrogen atom, halogen or methyl,        -   R^(38a) represents a hydrogen atom, halogen or methyl,        -   R³⁹ represents a hydrogen atom, cyano, fluorine or            (C₁-C₄)-alkylsulfanyl,        -   R^(39a) represents a hydrogen atom, cyano, fluorine or            (C₁-C₄)-alkylsulfanyl,        -   R⁴⁰ represents a hydrogen atom, halogen, cyano, hydroxy,            —(CH₂)_(n)NR¹⁶R¹⁷, (C₁-C₄)-alkyl, (C₁-C₄)-alkoxy or            (C₁-C₄)-alkoxycarbonyl,            -   wherein said (C₁-C₄)-alkyl is optionally substituted                with cyano and optionally with up to five fluorine                atoms,            -   wherein said (C₁-C₄)-alkoxy is optionally substituted                with up to five fluorine atoms,            -   wherein            -   n represents 0 or 1,            -   R¹⁶ represents a hydrogen atom or (C₁-C₄)-alkyl,                -   wherein said (C₁-C₄)-alkyl is optionally substituted                    with up to five fluorine atoms,            -   R¹⁷ represents a hydrogen atom or (C₁-C₄)-alkyl,                -   wherein said (C₁-C₄)-alkyl is optionally substituted                    with up to five fluorine atoms,            -   or            -   R¹⁶ and R¹⁷ together with the nitrogen atom they are                attached form a 4- to 8-membered heterocycle            -   wherein said 4- to 8-membered heterocycle is optionally                substituted, identically or differently, with one, two                or three groups selected from (C₁-C₄)-alkyl and                optionally up to five fluorine atoms,        -   wherein said 6-membered heteroaryl group is optionally            substituted, identically or differently, with one or two            groups selected from a halogen atom, cyano, (C₁-C₄)-alkyl,            and (C₁-C₄)-alkoxy,            -   wherein said (C₁-C₄)-alkyl is optionally substituted                with up to five fluorine atoms,            -   wherein said (C₁-C₄)-alkoxy is optionally substituted                with up to three fluorine atoms,        -   wherein said 2-oxopyridin-1(2H)-yl is optionally            substituted, identically or differently, with one or two            groups selected from a halogen atom, cyano, (C₁-C₄)-alkyl            and (C₁-C₄)-alkoxy,            -   wherein said (C₁-C₄)-alkyl is optionally substituted                with up to five fluorine atoms,            -   wherein said (C₁-C₄)-alkoxy is optionally substituted                with up to three fluorine atoms,        -   wherein said 4- to 8-membered heterocycle is optionally            substituted, identically or differently, with one, two or            three groups selected from (C₁-C₄)-alkyl, cyano,            (C₁-C₄)-alkoxycarbonyl and optionally up to five fluorine            atoms,            -   wherein said (C₁-C₄)-alkyl is optionally substituted                with up to five fluorine atoms,        -   wherein said (C₄-C₈)-cycloalkyl is optionally substituted,            identically or differently, with one or two groups selected            from (C₁-C₄)-alkyl, cyano and optionally up to five fluorine            atoms,            -   wherein said (C₁-C₄)-alkyl is optionally substituted                with (C₃-C₆)-cycloalkyl and optionally up to five                fluorine atoms,

    -   R⁷ represents a hydrogen atom, (C₁-C₄)-alkyl, a phenyl group, a        5- to 6-membered heteroaryl group or (C₁-C₄)-alkylsulfonyl,        -   wherein any phenyl group and any 5- to 6-membered heteroaryl            are each optionally substituted, identically or differently,            with one, two or three groups selected from a halogen atom,            (C₁-C₄)-alkyl, trifluoromethyl, (C₁-C₄)-alkoxy and            trifluoromethoxy,        -   wherein said (C₁-C₄)-alkyl is optionally substituted with a            group selected from (C₃-C₆)-cycloalkyl, 4- to 6-membered            heterocycle, hydroxy, —NR²⁰R²¹, (C₁-C₄)-alkoxy or benzyloxy            and optionally with up to five fluorine atoms,            -   wherein said (C₃-C₆)-cycloalkyl is optionally                substituted, identically or differently, with one or two                groups selected from (C₁-C₄)-alkyl, hydroxy and up to                five fluorine atoms,            -   wherein said 4- to 6-membered heterocycle is optionally                substituted, identically or differently, with one or two                groups selected from (C₁-C₄)-alkyl and optionally up to                five fluorine atoms,            -   and            -   wherein            -   R²⁰ represents a hydrogen atom or (C₁-C₄)-alkyl,            -   R²¹ represents a hydrogen atom or (C₁-C₄)-alkyl,            -   or            -   R²⁰ and R²¹ together with the nitrogen atom they are                attached form a 4- to 6-membered heterocycle                -   wherein said 4- to 6-membered heterocycle is                    optionally substituted, identically or differently,                    with one, two or three groups selected from                    (C₁-C₄)-alkyl and optionally up to five fluorine                    atoms,

    -   with the proviso that if R⁵ is (C₁-C₄)-alkoxy then R⁷ is        different from hydrogen,

    -   with the proviso that if R⁶ is 6-membered heteroaryl then R⁷ is        different from hydrogen,

    -   with the proviso that if R⁶ is 2-oxopyridin-1(2H)-yl then R⁷ is        different from hydrogen,

    -   with the proviso that if R⁶ is a 4- to 8-membered heterocycle        then R⁷ is different from hydrogen,

    -   R⁸ represents a group selected from a halogen atom, cyano,        (C₁-C₄)-alkyl, (C₁-C₄)-alkoxy, (C₃-C₆)-cycloalkyl, 4- to        6-membered heterocycle, (C₁-C₄)-alkylcarbonyl and a phenyl        group,        -   wherein said (C₁-C₄)-alkyl is optionally substituted,            identically or differently, with one or two groups selected            from —NR²²R²³ (C₁-C₄)-alkoxy and cyclopropyl and optionally            up to five fluorine atoms,            -   wherein said cyclopropyl is optionally substituted with                up to four fluorine atoms,            -   wherein said (C₁-C₄)-alkoxy is optionally substituted                with up to five fluorine atoms,            -   wherein            -   R²² represents a hydrogen atom or (C₁-C₄)-alkyl,            -   R²³ represents a hydrogen atom or (C₁-C₄)-alkyl,            -   or            -   R²² and R²³ together with the nitrogen atom they are                attached form a 4- to 6-membered heterocycle                -   wherein said 4- to 6-membered heterocycle is                    optionally substituted, identically or differently,                    with one, two or three groups selected from                    (C₁-C₄)-alkyl and optionally up to five fluorine                    atoms,        -   wherein said (C₁-C₄)-alkoxy is optionally substituted with            up to five fluorine atoms,        -   wherein said (C₃-C₆)-cycloalkyl is optionally substituted,            identically or differently, with one or two groups selected            from (C₁-C₄)-alkyl and optionally up to five fluorine atoms,        -   wherein said 4- to 6-membered heterocycle is optionally            substituted, identically or differently, with one or two            groups selected from (C₁-C₄)-alkyl and optionally up to five            fluorine atoms,        -   and        -   wherein said phenyl group is optionally substituted,            identically or differently, with one, two or three groups            selected from a halogen atom, cyano, (C₁-C₄)-alkyl,            trifluoromethyl, (C₁-C₄)-alkoxy and trifluoromethoxy,

    -   R⁹ represents 6-membered heteroaryl, 2-oxopyridin-1(2H)-yl,        (C₃-C₈)-cycloalkyl, a 4- to 8-membered heterocycle or        (C₁-C₄)-alkyl,        -   or        -   represents a group of the formula

-   -   -   in which        -   ## represents the point of attachment to the pyrazole ring,        -   R^(38b) represents a hydrogen atom, halogen or methyl,        -   R^(38c) represents a hydrogen atom, halogen or methyl,        -   R^(39b) represents a hydrogen atom, cyano, fluorine or            (C₁-C₄)-alkylsulfanyl,        -   R^(39c) represents a hydrogen atom, cyano, fluorine or            (C₁-C₄)-alkylsulfanyl,        -   R^(40a) represents a hydrogen atom, halogen, cyano, hydroxy,            —(CH₂)_(n)NR^(16a)R^(l7a), (C₁-C₄)-alkyl, (C₁-C₄)-alkoxy,            (C₁-C₄)-alkoxycarbonyl, a 4- to 6-membered heterocycle,            cyclopropyl or cyclobutyl,            -   wherein said (C₁-C₄)-alkyl is optionally substituted                with cyano and optionally with up to five fluorine                atoms,            -   wherein said (C₁-C₄)-alkoxy is optionally substituted                with up to five fluorine atoms,            -   wherein said 4- to 6-membered heterocycle is optionally                substituted, identically or differently, with one, two                or three groups selected from (C₁-C₄)-alkyl and                optionally up to five fluorine atoms,            -   wherein            -   n represents 0 or 1,            -   R^(16a) represents a hydrogen atom or (C₁-C₄)-alkyl,                -   wherein said (C₁-C₄)-alkyl is optionally substituted                    with up to five fluorine atoms,            -   R^(17a) represents a hydrogen atom or (C₁-C₄)-alkyl,                -   wherein said (C₁-C₄)-alkyl is optionally substituted                    with up to five fluorine atoms,            -   or            -   R^(16a) and R^(17a) together with the nitrogen atom they                are attached form a 4- to 8-membered heterocycle                -   wherein said 4- to 8-membered heterocycle is                    optionally substituted, identically or differently,                    with one, two or three groups selected from                    (C₁-C₄)-alkyl and optionally up to five fluorine                    atoms,        -   wherein said (C₁-C₄)-alkyl is optionally substituted with up            to five fluorine atoms,        -   wherein said 6-membered heteroaryl group is optionally            substituted, identically or differently, with one or two            groups selected from a halogen atom, cyano, (C₁-C₄)-alkyl,            and (C₁-C₄)-alkoxy,            -   wherein said (C₁-C₄)-alkyl is optionally substituted                with up to five fluorine atoms,            -   wherein said (C₁-C₄)-alkoxy is optionally substituted                with up to three fluorine atoms,        -   wherein said 2-oxopyridin-1(2H)-yl is optionally            substituted, identically or differently, with one or two            groups selected from a halogen atom, cyano, (C₁-C₄)-alkyl,            and (C₁-C₄)-alkoxy,            -   wherein said (C₁-C₄)-alkyl is optionally substituted                with up to five fluorine atoms,            -   wherein said (C₁-C₄)-alkoxy is optionally substituted                with up to three fluorine atoms,        -   wherein said (C₃-C₈)-cycloalkyl is optionally substituted,            identically or differently, with one or two groups selected            from (C₁-C₄)-alkyl, cyano and optionally up to five fluorine            atoms,            -   wherein said (C₁-C₄)-alkyl is optionally substituted                with (C₃-C₆)-cycloalkyl and optionally up to five                fluorine atoms,        -   wherein said 4- to 8-membered heterocycle is optionally            substituted identically or differently, with one or two            groups selected from (C₁-C₄)-alkyl, cyano,            (C₁-C₄)-alkoxycarbonyl and optionally up to five fluorine            atoms,            -   wherein said (C₁-C₄)-alkyl is optionally substituted                with up to five fluorine atoms,

    -   R¹⁰ represents a hydrogen atom, (C₁-C₄)-alkyl,        (C₃-C₅)-cycloalkyl, (C₁-C₄)-alkoxycarbonyl,        mono-(C₁-C₄)-alkylamino, a phenyl group or a 5- to 6-membered        heteroaryl group,        -   wherein any phenyl group and any 5- to 6-membered heteroaryl            are each optionally substituted, identically or differently,            with one, two or three groups selected from a halogen atom,            (C₁-C₄)-alkyl, trifluoromethyl, (C₁-C₄)-alkoxy and            trifluoromethoxy,        -   wherein said (C₁-C₄)-alkyl is optionally substituted with a            group selected from (C₃-C₆)-cycloalkyl, 5-membered            heteroaryl, —NR²⁸R²⁹, (C₁-C₄)-alkoxy or benzyloxy and            optionally with up to five fluorine atoms and is optionally            additionally substituted with hydroxy,            -   wherein said (C₃-C₆)-cycloalkyl is optionally                substituted, identically or differently, with hydroxy or                one or two groups (C₁-C₄)-alkyl and optionally up to                five fluorine atoms,            -   and            -   wherein            -   R²⁸ represents a hydrogen atom or (C₁-C₄)-alkyl,            -   R²⁹ represents a hydrogen atom or (C₁-C₄)-alkyl,            -   or            -   R²⁸ and R²⁹ together with the nitrogen atom they are                attached form a 4- to 6-membered heterocycle                -   wherein said 4- to 6-membered heterocycle is                    optionally substituted, identically or differently,                    with one, two or three groups selected from                    (C₁-C₄)-alkyl and optionally up to five fluorine                    atoms,            -   wherein said 5-membered heteroaryl is optionally                substituted with (C₁-C₄)-alkyl,

    -   with the proviso that if R⁹ is 6-membered heterorayl then R¹⁰ is        different from hydrogen,

    -   with the proviso that if R⁹ is 2-oxopyridin-1(2H)-yl then R¹⁰ is        different from hydrogen,

    -   with the proviso that if R⁹ is a 4- to 8-membered heterocycle        then R¹⁰ is different from hydrogen,

    -   with the proviso that if R⁸ is (C₁-C₄)-alkoxy then le° is        different from hydrogen,

    -   R¹¹ represents a group selected from a hydrogen atom, a fluorine        atom, a chlorine atom, (C₁-C₄)-alkyl and cyclopropyl,        -   wherein said (C₁-C₄)-alkyl is optionally substituted with            cyclopropyl and optionally up to five fluorine atoms,

    -   R¹² represents a 6-membered heteroaryl group,        2-oxopyridin-1(2H)-yl, (C₄-C₈)-cycloalkyl or (C₁-C₄)-alkyl,        -   or        -   represents a group of the formula

-   -   -   in which        -   ## represents the point of attachment to the pyrazole ring,        -   R^(38d) represents a hydrogen atom, halogen or methyl,        -   R^(38e) represents a hydrogen atom, halogen or methyl,        -   R^(39d) represents a hydrogen atom, cyano, fluorine or            (C₁-C₄)-alkylsulfanyl,        -   R^(39e) represents a hydrogen atom, cyano, fluorine or            (C₁-C₄)-alkylsulfanyl,        -   R^(40b) represents a hydrogen atom, halogen, cyano, hydroxy,            —(CH₂)_(n)NR^(16a)R^(17a), (C₁-C₄)-alkyl, (C₁-C₄)-alkoxy,            (C₁-C₄)-alkoxycarbonyl, a 4- to 6-membered heterocycle,            cyclopropyl or cyclobutyl,            -   wherein said (C₁-C₄)-alkyl is optionally substituted                with cyano and optionally with up to five fluorine                atoms,            -   wherein said (C₁-C₄)-alkoxy is optionally substituted                with up to five fluorine atoms,            -   wherein said 4- to 6-membered heterocycle is optionally                substituted, identically or differently, with one, two                or three groups selected from (C₁-C₄)-alkyl and                optionally up to five fluorine atoms,            -   wherein            -   n represents 0 or 1,            -   R^(16a) represents a hydrogen atom or (C₁-C₄)-alkyl,                -   wherein said (C₁-C₄)-alkyl is optionally substituted                    with up to five fluorine atoms,            -   R^(17a) represents a hydrogen atom or (C₁-C₄)-alkyl,                -   wherein said (C₁-C₄)-alkyl is optionally substituted                    with up to five fluorine atoms,            -   or            -   R^(16a) and R^(17a) together with the nitrogen atom they                are attached form a 4- to 8membered heterocycle,                -   wherein said 4- to 8-membered heterocycle is                    optionally substituted, identically or differently,                    with one, two or three groups selected from                    (C₁-C₄)-alkyl and optionally up to five fluorine                    atoms,        -   wherein said 6-membered heteroaryl group is optionally            substituted, identically or differently, with one or two            groups selected from a halogen atom, cyano, (C₁-C₄)-alkyl,            and (C₁-C₄)-alkoxy,            -   wherein said (C₁-C₄)-alkyl is optionally substituted                with up to five fluorine atoms,            -   wherein said (C₁-C₄)-alkoxy is optionally substituted                with up to three fluorine atoms,        -   wherein said 2-oxopyridin-1(2H)-yl is optionally            substituted, identically or differently, with one or two            groups selected from a halogen atom, cyano, (C₁-C₄)-alkyl,            and (C₁-C₄)-alkoxy,            -   wherein said (C₁-C₄)-alkyl is optionally substituted                with up to five fluorine atoms,            -   wherein said (C₁-C₄)-alkoxy is optionally substituted                with up to three fluorine atoms,        -   wherein said (C₄-C₈)-cycloalkyl is optionally substituted,            identically or differently, with one or two groups selected            from (C₁-C₄)-alkyl or cyano and optionally up to five            fluorine atoms,

    -   R¹³ represents a group selected from a hydrogen atom, a fluorine        atom, a chlorine atom, (C₁-C₄)-alkyl and cyclopropyl,        -   wherein said (C₁-C₄)-alkyl is optionally substituted with            cyclopropyl and up to five fluorine atoms,

-   R² represents a group selected from a hydrogen atom, (C₁-C₄)-alkyl,    (C₃-C₆)-cycloalkyl and (C₁-C₄)-alkoxycarbonyl,    -   wherein said (C₁-C₄)-alkyl is optionally substituted,        identically or differently, with one or two groups selected from        hydroxy, (C₁-C₄)-alkoxy, cyclopropyl and optionally up to five        fluorine atoms,

-   R³ represents a group selected from a hydrogen atom, a halogen atom,    cyano, hydroxy, nitro, amino, mono-(C₁-C₄)-alkylamino,    di-(C₁-C₄)-alkylamino, (C₁-C₄)-alkylsulfanyl, (C₁-C₄)-alkylsulfinyl,    (C₁-C₄)-alkylsulfonyl, (C₁-C₆)-alkyl, (C₁-C₄)-alkoxy,    (C₃-C₆)-cycloalkyl, 4- to 6-membered heterocycle, 5- to 6-membered    heteroaryl, —(CH₂)_(q)C(═O)—NR³⁴R³⁵, —O—C(═O)—NR³⁶R³⁷,    —O—C(═O)—OR^(37a), —NH—C(═)—NR³⁶R³⁷, —N(CH₃)—C(═O)—NR³⁶R³⁷,    —NH—C(═O)—OR^(37a), —N(CH₃)—C(═O)—OR^(37a)—NH—C(═O)—R³⁷,    —N(CH₃)—C(═O)—R³⁷, (C₁-C₄)-alkylcarbonyl, (C₁-C₄)-alkylcarbonyloxy    and (C₁-C₄)-alkoxycarbonyl,    -   wherein said (C₁-C₆)-alkyl is optionally substituted,        identically or differently, with one or two groups selected from        hydroxy, amino, mono-(C₁-C₄)-alkylamino, di-(C₁-C₄)-alkylamino,        cyano, (C₁-C₄)-alkoxy, 4- to 6-membered heterocycle,        (C₁-C₄)-alkoxycarbonyl and cyclopropyl and optionally up to six        fluorine atoms,        -   wherein said 4- to 6-membered heterocycle is optionally            substituted with (C₁-C₄)-alkyl or cyclopropyl and optionally            up to two fluorine atoms,    -   wherein said (C₁-C₄)-alkoxy is optionally substituted with        cyano, cyclopropyl and optionally up to five fluorine atoms,    -   wherein said (C₁-C₄)-alkyl of mono-(C₁-C₄)-alkylamino is        optionally substituted with cyano, cyclopropyl and optionally up        to five fluorine atoms,    -   wherein said di-(C₁-C₄)-alkylamino is optionally substituted        with cyano, cyclopropyl and optionally up to five fluorine        atoms,    -   wherein said (C₃-C₆)-cycloalkyl is optionally substituted,        identically or differently, with one or two groups selected from        (C₁-C₄)-alkyl, (C₁-C₄)-alkoxy, hydroxy and cyclopropyl and        optionally up to five fluorine atoms,    -   wherein said 4- to 6-membered heterocycle is optionally        substituted, identically or differently, with one or two groups        selected from (C₁-C₄)-alkyl, trifluoromethyl, difluoromethyl,        (C₁-C₄)-alkoxy, (C₁-C₄)-alkoxycarbonyl,        mono-(C₁-C₄)-alkylaminocarbonyl, di-(C₁-C₄)-alkylaminocarbonyl,        (C₁-C₄)-alkylcarbonyl, hydroxy and cyclopropyl and optionally up        to five fluorine atoms,    -   wherein said 5- to 6-membered heteroaryl is optionally        substituted, identically or differently, with one or two groups        selected from (C₁-C₄)-alkyl, (C₁-C₄)-alkoxy, and cyclopropyl and        optionally up to five fluorine atoms,    -   wherein    -   q represents 0 or 1,    -   R³⁴ represents a hydrogen atom or (C₁-C₄)-alkyl,    -   R³⁵ represents a hydrogen atom, (C₁-C₄)-alkyl or phenyl,    -   or    -   R³⁴ and R³⁵ together with the nitrogen atom they are attached        form a 4- to 7-membered heterocyclyl ring        -   wherein said 4- to 7-membered heterocyclyl ring is            optionally substituted, identically or differently, with            one, two or three groups selected from a fluorine atom,            hydroxy, (C₁-C₄)-alkyl, (C₁-C₄)-alkoxy, cyclopropyl,            difluoromethyl, trifluoromethyl and trifluoromethoxy,    -   wherein    -   R³⁶ represents a hydrogen atom or methyl,    -   R³⁷ represents a hydrogen atom, methyl, difluoromethyl,        trifluoromethyl or cyclopropyl,    -   R^(37a) represents methyl, difluoromethyl, trifluoromethyl or        cyclopropyl,

with the proviso that if R³ is —(CH₂)_(q)C(═O)—NR³⁴R³⁵,—O—C(═O)—NR³⁶R³⁷, —O—C(═O)—OR^(37a), —N(CH₃)—C(═O)—NR³⁶R³⁷,—NH—C(═O)—OR^(37a), —NH—C(═O)—NR³⁶R³⁷,—N(CH₃)—C(═O)—OR^(37a)—NH—C(═O)—R³⁷ or —N(CH₃)—C(═O)—R³⁷, then R⁷ andR¹⁰ are different from hydrogen,

with the proviso that if R³ is cyano then R² and R⁴ are different fromhydrogen,

with the proviso that if R³ is cyano then R⁶ and R⁹ are different from6-membered heteroaryl,

or

R² and R³ together with the carbon atoms they are attached form a 4- to6-membered carbocycle, a 4- to 7-membered azaheterocycle, a 4- to7-membered oxaheterocycle, a 5- to 6-membered heteroaryl group or aphenyl ring,

-   -   wherein said 4- to 7-membered azaheterocycle is optionally        substituted, identically or differently, with one or two groups        selected from hydroxy, oxo, (C₁-C₄)-alkyl, trifluoromethyl,        (C₁-C₄)-alkylcarbonyl and (C₁-C₄)-alkoxycarbonyl and optionally        up to five fluorine atoms,    -   wherein said 4- to 7-membered oxaheterocycle is optionally        substituted, identically or differently, with one or two groups        selected from hydroxy, oxo, (C₁-C₄)-alkyl, trifluoromethyl,        (C₁-C₄)-alkylcarbonyl and (C₁-C₄)-alkoxycarbonyl and optionally        up to five fluorine atoms,    -   wherein said 4- to 6-membered carbocycle is optionally        substituted, identically or differently, with one or two groups        selected from hydroxy, oxo, amino, mono-(C₁-C₄)-alkylamino,        di-(C₁-C₄)-alkylamino, (C₁-C₄)-alkyl, trifluoromethyl,        (C₁-C₄)-alkylcarbonyl and (C₁-C₄)-alkoxycarbonyl and optionally        up to five fluorine atoms,    -   and    -   wherein any phenyl group and any 5- to 6-membered heteroaryl        group are each optionally substituted, identically or        differently, with one, two or three groups selected from a        halogen atom, (C₁-C₄)-alkyl, trifluoromethyl, (C₁-C₄)-alkoxy and        trifluoromethoxy,

with the proviso that if R² and R³ together with the carbon atoms theyare attached to form a 4- to 7-membered azaheterocycle with anon-substituted nitrogen atom which is not directly attached to thepyrazole, then R⁷ and R¹⁰ are different from hydrogen,

with the proviso that if R⁷ and R¹⁰ are hydrogen then the nitrogen atomof the 4- to 7-membered azaheterocycle formed by le and R³ together withthe carbon atoms they are attached to is substituted with (C₁-C₄)-alkylor (C₁-C₄)-alkoxycarbonyl,

-   R⁴ represents a group selected from a hydrogen atom, (C₁-C₄)-alkyl,    (C₃-C₆)-cycloalkyl and (C₁-C₄)-alkoxycarbonyl and hydroxy,    -   wherein said (C₁-C₄)-alkyl is optionally substituted,        identically or differently, with one or two groups selected from        hydroxy, (C₁-C₄)-alkoxy and cyclopropyl and optionally up to        five fluorine atoms,

or

R³ and R⁴ together with the carbon atoms they are attached form a 4- to6-membered carbocycle, a 4- to 7-membered heterocycle, a 5- to6-membered heteroaryl group or a phenyl ring,

-   -   wherein said 4- to 7-membered heterocycle is optionally        substituted, identically or differently, with one or two groups        selected from a fluorine atom, hydroxy, oxo, (C₁-C₄)-alkyl,        trifluoromethyl, (C₁-C₄)-alkylcarbonyl and        (C₁-C₄)-alkoxycarbonyl and optionally up to five fluorine atoms,

wherein said 4- to 6-membered carbocycle is optionally substituted,identically or differently, with one or two groups selected from afluorine atom, hydroxy, oxo, (C₁-C₄)-alkyl, trifluoromethyl,(C₁-C₄)-alkylcarbonyl and (C₁-C₄)-alkoxycarbonyl and optionally up tofive fluorine atoms,

-   -   and    -   wherein any phenyl group and any 5- to 6-membered heteroaryl        group are each optionally substituted, identically or        differently, with one, two or three groups selected from a        halogen atom, (C₁-C₄)-alkyl, trifluoromethyl, (C₁-C₄)-alkoxy and        trifluoromethoxy,

with the proviso that if R³ and R⁴ together with the carbon atoms theyare attached form a 4- to 7-membered heterocycle with a non-substitutednitrogen atom which is not directly attached to the pyrazole, then R⁷and R¹⁰ is different from hydrogen,

with the proviso that if R⁷ and R¹⁰ are hydrogen then the nitrogen atomof the 4- to 7-membered heterocycle formed by R³ and R⁴ together withthe carbon atoms they are attached to is substituted with (C₁-C₄)-alkylor (C₁-C₄)-alkoxycarbonyl,

or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or asalt thereof, or a mixture of same.

The term “substituted” means that one or more hydrogen atoms on thedesignated atom or group are replaced with a selection from theindicated group, provided that the designated atom's normal valencyunder the existing circumstances is not exceeded. Combinations ofsubstituents and/or variables are permissible.

The term “optionally substituted” means that the number of substituentscan be equal to or different from zero. Unless otherwise indicated, itis possible that optionally substituted groups are substituted with asmany optional substituents as can be accommodated by replacing ahydrogen atom with a non-hydrogen substituent on any available carbonatom or heteroatom. Commonly, it is possible for the number of optionalsubstituents, when present, to be 1, 2, 3, 4 or 5, in particular 1, 2 or3.

As used herein, the term “one or more”, e.g. in the definition of thesubstituents of the compounds of general formula (I) of the presentinvention, means “1, 2, 3, 4 or 5, particularly 1, 2, 3 or 4, moreparticularly 1, 2 or 3, even more particularly 1 or 2”.

When groups in the compounds according to the invention are substituted,it is possible for said groups to be mono-substituted orpoly-substituted with substituent(s), unless otherwise specified. Withinthe scope of the present invention, the meanings of all groups whichoccur repeatedly are independent from one another. It is possible thatgroups in the compounds according to the invention are substituted withone, two or three identical or different substituents.

As used herein, an oxo substituent represents an oxygen atom, which isbound to a carbon atom or to a sulfur atom via a double bond.

The term “ring substituent” means a substituent attached to an aromaticor nonaromatic ring which replaces an available hydrogen atom on thering.

The term “comprising” when used in the specification includes“consisting of”.

If within the present text any item is referred to as “as mentionedherein”, it means that it may be mentioned anywhere in the present text.

The terms as mentioned in the present text have the following meanings:

The term “halogen atom” means a fluorine, chlorine, bromine or iodineatom, particularly a fluorine, chlorine or bromine atom, even moreparticularly fluorine or chlorine.

The term “C₁-C₄-alkyl” and “C₁-C₆-alkyl” means a linear or branched,saturated, monovalent hydrocarbon group having 1, 2, 3, or 4 carbonatoms, and 1, 2, 3, 4, 5 or 6 carbon atoms, e.g. a methyl, ethyl,propyl, isopropyl, butyl, sec-butyl, isobutyl, tert-butyl, pentyl,isopentyl, 2-methylbutyl, 1-methylbutyl, 1-ethylpropyl,1,2-dimethylpropyl, neo-pentyl, 1,1-dimethylpropyl, hexyl,1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl,1-ethylbutyl, 2-ethylbutyl, 1,1-dimethylbutyl, 2,2-dimethylbutyl,3,3-dimethylbutyl, 2,3-dimethylbutyl, 1,2-dimethylbutyl or1,3-dimethylbutyl group, or an isomer thereof. Particularly, said grouphas 1, 2, 3 or 4 carbon atoms (“C₁-C₄-alkyl”), e.g. a methyl, ethyl,propyl, isopropyl, butyl, sec-butyl isobutyl, or tert-butyl group, moreparticularly 1, 2 or 3 carbon atoms (“C₁-C₃-alkyl”), e.g. a methyl,ethyl, n-propyl or isopropyl group.

The term “(C₁-C₄)-alkylsulfanyl” means a linear or branched, saturated,monovalent group of formula (C₁-C₆-alkyl)—S—, in which the term“C₁-C₄-alkyl” is as defined supra, e.g. a methylsulfanyl, ethylsulfanyl,ppropylsulfanyl, isopropylsulfanyl, butylsulfanyl, sec-butylsulfanyl,isobutylsulfanyl, tert-butylsulfanyl group.

The term “C₁-C₄-alkoxy” means a linear or branched, saturated,monovalent group of formula (C₁-C₄-alkyl)-O—, in which the term“C₁-C₄-alkyl” is as defined supra, e.g. a methoxy, ethoxy, n-propoxy,isopropoxy, n-butoxy, sec-butoxy, isobutoxy, tert-butoxy, or an isomerthereof.

The term “C₃-C₆-cycloalkyl” and “C₅-C₆-cycloalkyl” means a saturated,monovalent, mono- or bicyclic hydrocarbon ring which contains 3, 4, 5 or6 carbon atoms (“C₃-C₆-cycloalkyl”). Said C₃-C₆-cycloalkyl group is forexample, a monocyclic hydrocarbon ring, e.g. a cyclopropyl, cyclobutyl,cyclopentyl or cyclohexyl group, or a bicyclic hydrocarbon ring. Theterm “3- to 6-membered cycloalkyl” is equivalent to a“C₃-C₆-cycloalkyl”, Thus a “4-membered cycloalkyl group” has the samemeaning as a “C₄-cycloalkyl group”.

The terms “(C₃-C₆)-cycloalky”l and “C₃-C₈-cycloalkyl” mean a saturated,monovalent, mono- or bicyclic hydrocarbon ring which contains 3, 4, 5,6, 7 or 8 carbon atoms (“C₃-C₈-cycloalkyl”). Said C₃-C₈-cycloalkyl groupis for example, a monocyclic hydrocarbon ring, e.g. a cyclopropyl,cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl or cyclooctyl group, ora bicyclic hydrocarbon ring, e.g. a bicyclo[4.2.0]octyl oroctahydropentalenyl.

The term “3- to 6-membered heterocycle”, “4-membered heterocycle”, “4-to 6-membered heterocycle”, “5- to 6-membered heterocycle”, “3- to8-membered heterocycle” and 4- to 8-membered heterocycle means amonocyclic, saturated heterocycle with 3 to 8, 4 to 8, 3 to 6, 4 to 6 or4 or 5 or 6, ring atoms in total, respectively, which contains one ortwo identical or different ring heteroatoms from the series N, S or O,it being possible for said heterocycloalkyl group to be attached to therest of the molecule via any one of the carbon atoms. A heterocycloalkylgroup which contains at least one ring nitrogen atom may be namedaza-heterocyloalkyl, respectively a heterocycloalkyl group whichcontains at least one ring oxygen atom may be named oxa-heterocyloalkyl.In particular, an aza-heterocyloalkyl group contains only ring nitrogenatoms and an oxa-heterocyloalkyl group contains only ring oxygen atoms.

Said heterocycle, without being limited thereto, can be a 4-memberedring, such as azetidinyl, oxetanyl or thietanyl, for example; or a5-membered ring, such as tetrahydrofuranyl, 1,3-dioxolanyl, thiolanyl,pyrrolidinyl, imidazolidinyl, pyrazolidinyl, 1,1-dioxidothiolanyl,1,2-oxazolidinyl, 1,3-oxazolidinyl or 1,3-thiazolidinyl, for example; ora 6-membered ring, such as tetrahydropyranyl, tetrahydrothiopyranyl,piperidinyl, morpholinyl, dithianyl, thiomorpholinyl, piperazinyl,1,3-dioxanyl, 1,4-dioxanyl or 1,2-oxazinanyl, for example, or a7-membered ring, such as azepanyl, 1,4-diazepanyl or 1,4-oxazepanyl, forexample.

The terms “azaheterocyclyl” and “azaheterocycle” in the context of theinvention mean a monocyclic or bicyclic, saturated or partly unsaturatedheterocycle which has the particular number of ring atoms specified,contains a nitrogen atom and may additionally contain one or two furtherring heteroatom(s) from the group of N, O, S, SO and/or SO₂, and isjoined via a ring nitrogen atom. Preferred examples include:pyrrolidinyl, pyrazolidinyl, piperidinyl, piperazinyl, morpholinyl,thiomorpholinyl, 1,1-dioxothiomorpholinyl, hexahydroazepinyl,hexahydro-1,4-diazepinyl, 1,2,3,4-tetrahydroisoquinolinyl,1,2,3,4-tetrahy droquinolinyl, indolinyl, 8-azabicyclo[3.2.1]octanyl,9-azabicyclo[3.3.1]nonanyl, 3-azabicyclo[4.1.0]heptanyl andquinuclidinyl.

The terms “oxaheterocyclyl” and “oxaheterocycle” in the context of theinvention mean a monocyclic or bicyclic, saturated or partly unsaturatedheterocycle which has the particular number of ring atoms specified,contains an oxygen atom and may additionally contain one or two furtherring heteroatom(s) from the group of N, O, S, SO and/or SO₂,

The term “5- to 6-membered heteroaryl”, “5-membered heteroaryl” and“6-membered heteroaryl” means a monovalent, monocyclic aromatic ringwith 5 to 6, or 5 or 6, ring atoms in total, respectively, 5 or 6 ringatoms, which contains at least one ring heteroatom and optionally one,two or three further ring heteroatoms from the series: N, O and/or S,and which is bound via a ring carbon atom or optionally via a ringnitrogen atom (if allowed by valency).

Said heteroaryl group can be a 5-membered heteroaryl group, such as, forexample, thienyl, furanyl, pyrrolyl, oxazolyl, thiazolyl, imidazolyl,pyrazolyl, isoxazolyl, isothiazolyl, oxadiazolyl, triazolyl,thia-diazolyl or tetrazolyl; or a 6-membered heteroaryl group, such as,for example, pyridinyl, pyridazinyl, pyrimidinyl, pyrazinyl ortriazinyl; or a tricyclic heteroaryl group, such as, for example,carbazolyl, acridinyl or phenazinyl

mono-(C₁-C₄)-alkylamino in the context of the invention means an aminogroup with one straight-chain or branched alkyl substituent whichcontains 1, 2, 3 or 4 carbon atoms, such as: methylamino, ethylamino,n-propylamino, isopropylamino, n-butylamino, and tert-butylamino, forexample.

di-(C₁-C₄)-alkylamino in the context of the invention means an aminogroup with two identical or different straight-chain or branched alkylsubstituents which each contain 1, 2, 3 or 4 carbon atoms, such as:N,N-dimethylamino, N,N-diethylamino, N-ethyl-N-methylamino,N-methyl-N-n-propylamino, N-isopropyl-N-methylamino,N-isopropyl-N-n-propylamino, N,N-diisopropylamino,N-n-butyl-N-methylamino, and N-tert-butyl-N-methylamino, for example.

(C₁-C₄)-Alkylcarbonyl in the context of the invention means astraight-chain or branched alkyl group having 1, 2, 3 or 4 carbon atomswhich is bound to the rest of the molecule via a carbonyl group[—C(═O)—], such as: acetyl, propionyl, n-butyryl, isobutyryl,n-pentanoyl, and pivaloyl, for example.

(C₁-C₄)-Alkoxycarbonyl in the context of the invention means astraight-chain or branched alkoxy group having 1, 2, 3 or 4 carbon atomswhich is bound to the rest of the molecule via a carbonyl group[—C(═O)—], such as: methoxy carbonyl, ethoxy carbonyl, n-propoxycarbonyl, isopropoxy carbonyl, n-butoxycarbonyl, andtert-butoxycarbonyl, for example

mono-(C₁-C₄)-alkylaminocarbonyl in the context of the invention means anamino group which is bound to the rest of the molecule via a carbonylgroup [—C(αO)—] and which has one straight-chain or branched alkylsubstituent having 1, 2, 3 or 4 carbon atoms, such as:methylaminocarbonyl, ethylaminocarbonyl, n-propylaminocarbonyl,isopropylaminocarbonyl, n-butylaminocarbonyl, andtert-butylaminocarbonyl, for example.

di-(C₁-C₄)-alkylaminocarbonyl in the context of the invention means anamino group which is bound to the rest of the molecule via a carbonylgroup [—C(═O)—] and which has two identical or different straight-chainor branched alkyl substituents having in each case 1, 2, 3 or 4 carbonatoms, such as: N,N-dimethylaminocarbonyl, N,N-diethylaminocarbonyl,N-ethyl-N-methylaminocarbonyl, N-methyl-N-n-propylaminocarbonyl,N-isopropyl-N-methylaminocarbonyl, N,N-diisopropylaminocarbonyl,N-n-butyl-N-methylaminocarbonyl, and N-tert-butyl-N-methylaminocarbonyl,for example.

An oxo substituent in the context of the invention means an oxygen atom,which is bound to a carbon atom via a double bond

In general, and unless otherwise mentioned, the heteroaryl orheteroarylene groups include all possible isomeric forms thereof, e.g.:tautomers and positional isomers with respect to the point of linkage tothe rest of the molecule. Thus, for some illustrative non-restrictingexamples, the term pyridinyl includes pyridin-2-yl, pyridin-3-yl andpyridin-4-yl; or the term thienyl includes thien-2-yl and thien-3-yl.

The term “C₁-C₄”, as used in the present text, e.g. in the context ofthe definition of “C₁-C₄-alkyl”, “C₁-C₄-alkoxy”, “or“C₁-C₄-alkylsulfanyl”, means an alkyl group having a finite number ofcarbon atoms of 1 to 4, i.e. 1, 2, 3, or 4 carbon atoms.

The term “C₁-C₆”, as used in the present text, e.g. in the context ofthe definition of “C₁-C₆-alkyl”, means an alkyl group having a finitenumber of carbon atoms of 1 to 6, i.e. 1, 2, 3, 4, 5 or 6 carbon atoms.

Further, as used herein, the term “C₃-C₆”, as used in the present text,e.g. in the context of the definition of “C₃-C₆-cycloalkyl”, means acycloalkyl group having a finite number of carbon atoms of 3 to 6, i.e.3, 4, 5 or 6 carbon atoms.

Further, as used herein, the term “C₃-C₈”, as used in the present text,e.g. in the context of the definition of “C₃-C₈-cycloalkyl”, means acycloalkyl group having a finite number of carbon atoms of 3 to 8, i.e.3, 4, 5, 6, 7 or 8 carbon atoms.

When a range of values is given, said range encompasses each value andsub-range within said range.

For example

“C₁-C₄” encompasses C₁, C₂, C₃, C₄, C₁-C₄, C₁-C₃, C₁-C₂, C₂-C₄, C₂-C₃,and C₃-C₄;

“C₁-C₃” encompasses C₁, C₂, C₃, C₁-C₃, C₁-C₂, and C₂-C₃;

“C₂-C₄” encompasses C₂, C₃, C₄, C₂-C₄, C₂-C₃, and C₃-C₄;

“C₃-C₆” encompasses C₃, C₄, C₅, C₆, C₃-C₆, C₃-C₅, C₃-C₄, C₄-C₆, C₄-C₅,and C₅-C₆;

As used herein, the term “leaving group” means an atom or a group ofatoms that is displaced in a chemical reaction as stable species takingwith it the bonding electrons. In particular, such a leaving group isselected from the group comprising: halide, in particular fluoride,chloride, bromide or iodide, (methylsulfonyl)oxy (me syl(ate), Ms),Ktrifluoromethypsulfonyll oxy (triflyl/(ate), Tf),[(nonafluorobutyl)sulfonyl]oxy (nonaflate, Nf), (phenylsulfonyl)oxy,[(4-methylphenyl)sulfonyl]oxy, [(4-bromophenyl)sulfonyl]oxy,[(4-nitrophenypsulfonyl]oxy, [(2-nitrophenyl)sulfonyl]oxy,[(4-isopropylphenyl)sulfonyl]oxy,[(2,4,6-triisopropylphenyl)sulfonyl]oxy,[(2,4,6-trimethylphenyl)sulfonyl]oxy, [(4-tert-butylphenyl)-sulfonyl]oxyand [(4-methoxyphenyl)sulfonyl]oxy.

It is possible for the compounds of general formula (I) to exist asisotopic variants. The invention therefore includes one or more isotopicvariant(s) of the compounds of general formula (I), particularlydeuterium-containing compounds of general formula (I).

The term “Isotopic variant” of a compound or a reagent is defined as acompound exhibiting an unnatural proportion of one or more of theisotopes that constitute such a compound.

The term “Isotopic variant of the compound of general formula (I)” isdefined as a compound of general formula (I) exhibiting an unnaturalproportion of one or more of the isotopes that constitute such acompound.

The expression “unnatural proportion” means a proportion of such isotopewhich is higher than its natural abundance. The natural abundances ofisotopes to be applied in this context are described in “IsotopicCompositions of the Elements 1997”, Pure Appl. Chem., 70(1), 217-235,1998.

Examples of such isotopes include stable and radioactive isotopes ofhydrogen, carbon, nitrogen, oxygen, phosphorus, sulfur, fluorine,chlorine, bromine and iodine, such as ²H (deuterium), ³H (tritium), ¹¹C,¹³C, ¹⁴C, ¹⁵N, ¹⁷O, ¹⁸O, ³²P, ³³P, ³³S, ³⁴S, ³⁵S, ³⁶S, ¹⁸F, ³⁶Cl, ⁸²Br,¹²³I, ¹²⁴I, ¹²⁵I, ¹²⁹I and ¹³¹I, respectively.

With respect to the treatment and/or prophylaxis of the disordersspecified herein the isotopic variant(s) of the compounds of generalformula (I) preferably contain deuterium (“deuterium-containingcompounds of general formula (I)”). Isotopic variants of the compoundsof general formula (I) in which one or more radioactive isotopes, suchas ³H or ¹⁴C, are incorporated are useful e.g. in drug and/or substratetissue distribution studies. These isotopes are particularly preferredfor the ease of their incorporation and detectability. Positron emittingisotopes such as ¹⁸F or ¹¹C may be incorporated into a compound ofgeneral formula (I). These isotopic variants of the compounds of generalformula (I) are useful for in vivo imaging applications.Deuterium-containing and ¹³C-containing compounds of general formula (I)can be used in mass spectrometry analyses in the context of preclinicalor clinical studies.

Isotopic variants of the compounds of general formula (I) can generallybe prepared by methods known to a person skilled in the art, such asthose described in the schemes and/or examples herein, by substituting areagent for an isotopic variant of said reagent, preferably for adeuterium-containing reagent. Depending on the desired sites ofdeuteration, in some cases deuterium from D₂O can be incorporated eitherdirectly into the compounds or into reagents that are useful forsynthesizing such compounds (Esaki et al., Tetrahedron, 2006, 62, 10954;Esaki et al., Chem. Eur. J., 2007, 13, 4052). Deuterium gas is also auseful reagent for incorporating deuterium into molecules. Catalyticdeuteration of olefinic bonds (H. J. Leis et al., Curr. Org. Chem.,1998, 2, 131; J. R. Morandi et al., J. Org. Chem., 1969, 34 (6), 1889)and acetylenic bonds (N. H. Khan, J. Am. Chem. Soc., 1952, 74 (12),3018; S. Chandrasekhar et al., Tetrahedron Letters, 2011, 52, 3865) is arapid route for incorporation of deuterium. Metal catalysts (i.e. Pd,Pt, and Rh) in the presence of deuterium gas can be used to directlyexchange deuterium for hydrogen in functional groups containinghydrocarbons (J. G. Atkinson et al., U.S. Pat. No. 3,966,781). A varietyof deuterated reagents and synthetic building blocks are commerciallyavailable from companies such as for example C/D/N Isotopes, Quebec,Canada; Cambridge Isotope Laboratories Inc., Andover, Mass., USA; andCombiPhos Catalysts, Inc., Princeton, N.J., USA. Further information onthe state of the art with respect to deuterium-hydrogen exchange isgiven for example in Hanzlik et al., J. Org. Chem. 55, 3992-3997, 1990;R. P. Hanzlik et al., Biochem. Biophys. Res. Commun 160, 844, 1989; P.J. Reider et al., J. Org. Chem. 52, 3326-3334, 1987; M. Jarman et al.,Carcinogenesis 16(4), 683-688, 1995; J. Atzrodt et al., Angew. Chem.,Int. Ed. 2007, 46, 7744; K. Matoishi et al., Chem. Commun. 2000,1519-1520; K. Kassahun et al., WO2012/112363.

The term “deuterium-containing compound of general formula (I)” isdefined as a compound of general formula (I), in which one or morehydrogen atom(s) is/are replaced by one or more deuterium atom(s) and inwhich the abundance of deuterium at each deuterated position of thecompound of general formula (I) is higher than the natural abundance ofdeuterium, which is about 0.015%. Particularly, in adeuterium-containing compound of general formula (I) the abundance ofdeuterium at each deuterated position of the compound of general formula(I) is higher than 10%, 20%, 30%, 40%, 50%, 60%, 70% or 80%, preferablyhigher than 90%, 95%, 96% or 97%, even more preferably higher than 98%or 99% at said position(s). It is understood that the abundance ofdeuterium at each deuterated position is independent of the abundance ofdeuterium at other deuterated position(s).

The selective incorporation of one or more deuterium atom(s) into acompound of general formula (I) may alter the physicochemical properties(such as for example acidity [C. L. Perrin, et al., J. Am. Chem. Soc.,2007, 129, 4490; A. Streitwieser et al., J. Am. Chem. Soc., 1963, 85,2759;], basicity [C. L. Perrin et al., J. Am. Chem. Soc., 2005, 127,9641; C. L. Perrin, et al., J. Am. Chem. Soc., 2003, 125, 15008; C. L.Perrin in Advances in Physical Organic Chemistry, 44, 144],lipophilicity [B. Testa et al., Int. J. Pharm., 1984, 19(3), 271])and/or the metabolic profile of the molecule and may result in changesin the ratio of parent compound to metabolites or in the amounts ofmetabolites formed. Such changes may result in certain therapeuticadvantages and hence may be preferred in some circumstances. Reducedrates of metabolism and metabolic switching, where the ratio ofmetabolites is changed, have been reported (A. E. Mutlib et al.,Toxicol. Appl. Pharmacol., 2000, 169, 102; D. J. Kushner et al., Can. J.Physiol. Pharmacol., 1999, 77, 79). These changes in the exposure toparent drug and metabolites can have important consequences with respectto the pharmacodynamics, tolerability and efficacy of adeuterium-containing compound of general formula (I). In some casesdeuterium substitution reduces or eliminates the formation of anundesired or toxic metabolite and enhances the formation of a desiredmetabolite (e.g. Nevirapine: A. M. Sharma et al., Chem. Res. Toxicol.,2013, 26, 410; Efavirenz: A. E. Mutlib et al., Toxicol. Appl.Pharmacol., 2000, 169, 102). In other cases the major effect ofdeuteration is to reduce the rate of systemic clearance. As a result,the biological half-life of the compound is increased. The potentialclinical benefits would include the ability to maintain similar systemicexposure with decreased peak levels and increased trough levels. Thiscould result in lower side effects and enhanced efficacy, depending onthe particular compound's pharmacokinetic/pharmacodynamic relationship.ML-337 (C. J. Wenthur et al., J. Med. Chem., 2013, 56, 5208) andOdanacatib (K. Kassahun et al., WO2012/112363) are examples for thisdeuterium effect. Still other cases have been reported in which reducedrates of metabolism result in an increase in exposure of the drugwithout changing the rate of systemic clearance (e.g. Rofecoxib: F.Schneider et al., Arzneim. Forsch./Drug. Res., 2006, 56, 295;Telaprevir: F. Maltais et al., J. Med. Chem., 2009, 52, 7993).Deuterated drugs showing this effect may have reduced dosingrequirements (e.g. lower number of doses or lower dosage to achieve thedesired effect) and/or may produce lower metabolite loads.

A compound of general formula (I) may have multiple potential sites ofattack for metabolism. To optimize the above-described effects onphysicochemical properties and metabolic profile, deuterium-containingcompounds of general formula (I) having a certain pattern of one or moredeuterium-hydrogen exchange(s) can be selected. Particularly, thedeuterium atom(s) of deuterium-containing compound(s) of general formula(I) is/are attached to a carbon atom and/or is/are located at thosepositions of the compound of general formula (I), which are sites ofattack for metabolizing enzymes such as e.g. cytochrome P₄₅₀.

In another embodiment the present invention concerns adeuterium-containing compound of general formula (I) having 1, 2, 3 or 4deuterium atoms, particularly with 1, 2 or 3 deuterium atoms.

Where the plural form of the word compounds, salts, polymorphs,hydrates, solvates and the like, is used herein, this is taken to meanalso a single compound, salt, polymorph, isomer, hydrate, solvate or thelike.

By “stable compound’ or “stable structure” is meant a compound that issufficiently robust to survive isolation to a useful degree of purityfrom a reaction mixture, and formulation into an efficacious therapeuticagent.

The compounds of the present invention optionally contain one or moreasymmetric centres, depending upon the location and nature of thevarious substituents desired. It is possible that one or more asymmetriccarbon atoms are present in the (R) or (S) configuration, which canresult in racemic mixtures in the case of a single asymmetric centre,and in diastereomeric mixtures in the case of multiple asymmetriccentres.

In certain instances, it is possible that asymmetry also be present dueto restricted rotation about a given bond, for example, the central bondadjoining two substituted aromatic rings of the specified compounds.

Preferred compounds are those which produce the more desirablebiological activity. Separated, pure or partially purified isomers andstereoisomers or racemic or diastereomeric mixtures of the compounds ofthe present invention are also included within the scope of the presentinvention. The purification and the separation of such materials can beaccomplished by standard techniques known in the art.

The optical isomers can be obtained by resolution of the racemicmixtures according to conventional processes, for example, by theformation of diastereoisomeric salts using an optically active acid orbase or formation of covalent diastereomers. Examples of appropriateacids are tartaric, diacetyltartaric, ditoluoyltartaric andcamphorsulfonic acid. Mixtures of diastereoisomers can be separated intotheir individual diastereomers on the basis of their physical and/orchemical differences by methods known in the art, for example, bychromatography or fractional crystallisation. The optically active basesor acids are then liberated from the separated diastereomeric salts. Adifferent process for separation of optical isomers involves the use ofchiral chromatography (e.g., HPLC columns using a chiral phase), with orwithout conventional derivatisation, optimally chosen to maximise theseparation of the enantiomers. Suitable HPLC columns using a chiralphase are commercially available, such as those manufactured by Daicel,e.g., Chiracel OD and Chiracel OJ, for example, among many others, whichare all routinely selectable. Enzymatic separations, with or withoutderivatisation, are also useful. The optically active compounds of thepresent invention can likewise be obtained by chiral syntheses utilizingoptically active starting materials.

In order to distinguish different types of isomers from each otherreference is made to IUPAC Rules Section E (Pure Appl Chem 45, 11-30,1976).

The present invention includes all possible stereoisomers of thecompounds of the present invention as single stereoisomers, or as anymixture of said stereoisomers, e.g. (R)- or (S)-isomers, in any ratio.Isolation of a single stereoisomer, e.g. a single enantiomer or a singlediastereomer, of a compound of the present invention is achieved by anysuitable state of the art method, such as chromatography, especiallychiral chromatography, for example.

Further, it is possible for the compounds of the present invention toexist as tautomers. For example, any compound of the present inventionwhich contains an imidazopyridine moiety as a heteroaryl group forexample can exist as a 1H tautomer, or a 3H tautomer, or even a mixturein any amount of the two tautomers, namely:

Moreover, in the course of the synthesis of the 1H-pyrazole group the1H-pyrazol-3-yl tautomer as well as its tautomer 1H-pyrazol-5-yltautomer are formed.

The present invention includes all possible tautomers of the compoundsof the present invention as single tautomers, or as any mixture of saidtautomers, in any ratio.

The present invention also covers useful forms of the compounds of thepresent invention, such as metabolites, hydrates, solvates, prodrugs,salts, in particular pharmaceutically acceptable salts, and/orco-precipitates.

The compounds of the present invention can exist as a hydrate, or as asolvate, wherein the compounds of the present invention contain polarsolvents, in particular water, methanol or ethanol for example, asstructural element of the crystal lattice of the compounds. It ispossible for the amount of polar solvents, in particular water, to existin a stoichiometric or non-stoichiometric ratio. In the case ofstoichiometric solvates, e.g. a hydrate, hemi-, (semi-), mono-, sesqui-,di-, tri-, tetra-, penta- etc. solvates or hydrates, respectively, arepossible. The present invention includes all such hydrates or solvates.

Further, it is possible for the compounds of the present invention toexist in free form, e.g. as a free base, or as a free acid, or as azwitterion, or to exist in the form of a salt, in particular as a freeacid. Said salt may be any salt, either an organic or inorganic additionsalt, particularly any pharmaceutically acceptable organic or inorganicaddition salt, which is customarily used in pharmacy, or which is used,for example, for isolating or purifying the compounds of the presentinvention.

The term “pharmaceutically acceptable salt” refers to an inorganic ororganic acid addition salt of a compound of the present invention. Forexample, see S. M. Berge, et al. “Pharmaceutical Salts,” J. Pharm. Sci.1977, 66, 1-19.

A suitable pharmaceutically acceptable salt of the compounds of thepresent invention may be, for example, an acid-addition salt of acompound of the present invention bearing a nitrogen atom, in a chain orin a ring, for example, which is sufficiently basic, such as anacid-addition salt with an inorganic acid, or “mineral acid”, such ashydrochloric, hydrobromic, hydroiodic, sulfuric, sulfamic, bisulfuric,phosphoric, or nitric acid, for example, or with an organic acid, suchas formic, acetic, acetoacetic, pyruvic, trifluoroacetic, propionic,butyric, hexanoic, heptanoic, undecanoic, lauric, benzoic, salicylic,2-(4-hydroxybenzoyl)-benzoic, camphoric, cinnamic,cyclopentanepropionic, digluconic, 3-hydroxy-2-naphthoic, nicotinic,pamoic, pectinic, 3-phenylpropionic, pivalic, 2-hydroxyethanesulfonic,itaconic, trifluoromethanesulfonic, dodecylsulfuric, ethane sulfonic ,benzene sulfonic , para-toluenesulfonic, methanesulfonic,2-naphthalenesulfonic, naphthalinedisulfonic, camphorsulfonic acid,citric, tartaric, stearic, lactic, oxalic, malonic, succinic, malic,adipic, alginic, maleic, fumaric, D-gluconic, mandelic, ascorbic,glucoheptanoic, glycerophosphoric, aspartic, sulfosalicylic, orthiocyanic acid, for example.

Further, another suitably pharmaceutically acceptable salt of a compoundof the present invention which is sufficiently acidic, is an alkalimetal salt, for example a sodium or potassium salt, an alkaline earthmetal salt, for example a calcium, magnesium or strontium salt, or analuminium or a zinc salt, or an ammonium salt derived from ammonia orfrom an organic primary, secondary or tertiary amine having 1 to 20carbon atoms, such as ethylamine, diethylamine, triethylamine,ethyldiisopropylamine, monoethanolamine, diethanolamine,triethanolamine, dicyclohexylamine, dimethylaminoethanol,diethylaminoethanol, tris(hydroxymethyl)aminomethane, procaine,dibenzylamine, N-methylmorpholine, arginine, lysine,1,2-ethylenediamine, N-methylpiperidine, N-methyl-glucamine,N,N-dimethyl-glucamine, N-ethyl-glucamine, 1,6-hexanediamine,glucosamine, sarcosine, serinol, 2-amino-1,3-propanediol,3-amino-1,2-propanediol, 4-amino-1,2,3-butanetriol, or a salt with aquarternary ammonium ion having 1 to 20 carbon atoms, such astetramethylammonium, tetraethylammonium, tetra(n-propyl)ammonium,tetra(n-butyl)ammonium, N-benzyl-N,N,N-trimethylammonium, choline orbenzalkonium.

In accordance with a preferred embodiment of the first aspect, thepresent invention covers a pharmaceutically acceptable salt of compoundsof general formula (I), (I-C), supra, which is an alkali metal salt, inparticular a sodium or potassium salt, or an ammonium salt derived froman organic tertiary amine, in particular choline.

Those skilled in the art will further recognise that it is possible foracid addition salts of the claimed compounds to be prepared by reactionof the compounds with the appropriate inorganic or organic acid via anyof a number of known methods. Alternatively, alkali and alkaline earthmetal salts of acidic compounds of the present invention are prepared byreacting the compounds of the present invention with the appropriatebase via a variety of known methods.

The present invention includes all possible salts of the compounds ofthe present invention as single salts, or as any mixture of said salts,in any ratio.

In the present text, in particular in the Experimental Section, for thesynthesis of intermediates and of examples of the present invention,when a compound is mentioned as a salt form with the corresponding baseor acid, the exact stoichiometric composition of said salt form, asobtained by the respective preparation and/or purification process, is,in most cases, unknown.

Unless specified otherwise, suffixes to chemical names or structuralformulae relating to salts, such as “hydrochloride”, “trifluoroacetate”,“sodium salt”, or “x HCl”, “x CF₃COOH”, “x Na⁺”, for example, mean asalt form, the stoichiometry of which salt form not being specified.

This applies analogously to cases in which synthesis intermediates orexample compounds or salts thereof have been obtained, by thepreparation and/or purification processes described, as solvates, suchas hydrates, with (if defined) unknown stoichiometric composition.

As used herein, the term “in vivo hydrolysable ester” means an in vivohydrolysable ester of a compound of the present invention containing acarboxy or hydroxy group, for example, a pharmaceutically acceptableester which is hydrolysed in the human or animal body to produce theparent acid or alcohol. Suitable pharmaceutically acceptable esters forcarboxy include for example alkyl, cycloalkyl and optionally substitutedphenylalkyl, in particular benzyl esters, C₁-C₆ alkoxymethyl esters,e.g. methoxymethyl, C₁-C₆ alkanoyloxymethyl esters, e.g.pivaloyloxymethyl, phthalidyl esters, C₃-C₈cycloalkoxy-carbonyloxy-C₁-C₆ alkyl esters, e.g.1-cyclohexylcarbonyloxyethyl; 1,3-dioxolen-2-onylmethyl esters, e.g.5-methyl-1,3-dioxolen-2-onylmethyl; and C₁-C₆-alkoxycarbonyloxyethylesters, e.g. 1-methoxycarbonyloxyethyl, it being possible for saidesters to be formed at any carboxy group in the compounds of the presentinvention.

An in vivo hydrolysable ester of a compound of the present inventioncontaining a hydroxy group includes inorganic esters such as phosphateesters and [alpha]-acyloxyalkyl ethers and related compounds which as aresult of the in vivo hydrolysis of the ester breakdown to give theparent hydroxy group. Examples of [alpha]-acyloxyalkyl ethers includeacetoxymethoxy and 2,2-dimethylpropionyloxymethoxy. A selection of invivo hydrolysable ester forming groups for hydroxy include alkanoyl,benzoyl, phenylacetyl and substituted benzoyl and phenylacetyl,alkoxycarbonyl (to give alkyl carbonate esters), dialkylcarbamoyl andN-(dialkylaminoethyl)-N-alkylcarbamoyl (to give carbamates),dialkylaminoacetyl and carboxyacetyl. The present invention covers allsuch esters.

Furthermore, the present invention includes all possible crystallineforms, or polymorphs, of the compounds of the present invention, eitheras single polymorph, or as a mixture of more than one polymorph, in anyratio.

Moreover, the present invention also includes prodrugs of the compoundsaccording to the invention. The term “prodrugs” here designatescompounds which themselves can be biologically active or inactive, butare converted (for example metabolically or hydrolytically) intocompounds according to the invention during their residence time in thebody.

Preference is given to compounds of the formula (I) in which

-   R¹ represents a group of the formula

-   -   in which    -   # represents the point of attachment to the amino group,    -   R⁵ represents a group selected from fluorine, chlorine, cyano,        (C₁-C₄)-alkyl, methoxy, ethoxy, (C₃-C₅)-cycloalkyl,        methylcarbonyl and ethylcarbonyl,        -   wherein said (C₁-C₄)-alkyl is optionally substituted,            identically or differently, with one or two groups selected            from -Nee, methoxy, ethoxy, difluoromethoxy,            trifluoromethoxy and cyclopropyl and optionally up to five            fluorine atoms,            -   wherein said cyclopropyl is optionally substituted with                up to four fluorine atoms,            -   wherein            -   R¹⁴ represents a hydrogen atom or (C₁-C₄)-alkyl,            -   R¹⁵ represents a hydrogen atom or (C₁-C₄)-alkyl,            -   or            -   R¹⁴ and R¹⁵ together with the nitrogen atom they are                attached form a 4- to 5-membered heterocycle                -   wherein said 4- to 5-membered heterocycle is                    optionally substituted, identically or differently,                    with one or two groups selected from (C₁-C₄)-alkyl,                    trifluormethyl, difluoromethyl and optionally up to                    five fluorine atoms,        -   wherein said methoxy and ethoxy are optionally substituted            with up to three fluorine atoms,        -   wherein said (C₃-C₅)-cycloalkyl is optionally substituted            with up to four fluorine atoms,    -   R⁶ represents pyridyl, pyrimidyl, 2-oxopyridin-1(2H)-yl,        (C₅-C₈)-cycloalkyl or a 6- to 8-membered heterocycle    -   or    -   represents a group of the formula

-   -   -   in which        -   ## represents the point of attachment to the pyrazole ring,        -   R³⁸ represents a hydrogen atom, halogen or methyl,        -   R^(38a) represents a hydrogen atom, halogen or methyl,        -   R³⁹ represents a hydrogen atom, cyano, fluorine or            (C₁-C₄)-alkylsulfanyl,        -   R^(39a) represents a hydrogen atom, cyano, fluorine or            (C₁-C₄)-alkylsulfanyl,        -   R⁴⁰ represents a hydrogen atom, fluorine, chlorine, cyano,            hydroxy, —(CH₂)_(n)NR¹⁶R¹⁷, (C₁-C₃)-alkyl, (C₁-C₃)-alkoxy or            (C₁-C₄)-alkoxycarbonyl,            -   wherein said (C₁-C₃)-alkyl is optionally substituted                with cyano and optionally with up to five fluorine                atoms,            -   wherein said (C₁-C₃)-alkoxy is optionally substituted                with up to five fluorine atoms,            -   wherein            -   n represents 0 or 1,            -   R¹⁶ represents a hydrogen atom or (C₁-C₄)-alkyl,            -   R¹⁷ represents a hydrogen atom or (C₁-C₄)-alkyl,            -   or            -   R¹⁶ and R¹⁷ together with the nitrogen atom they are                attached form a 4- to 6-membered heterocycle            -   wherein said 4- to 6-membered heterocycle is optionally                substituted, identically or differently, with one, two                or three groups selected from (C₁-C₄)-alkyl and                optionally up to five fluorine atoms,        -   wherein said pyridyl and pyrimidyl are optionally            substituted, identically or differently, with one or two            groups selected from a halogen atom, cyano, methyl, ethyl,            methoxy and ethoxy,            -   wherein said (C₁-C₄)-alkyl is optionally substituted                with up to five fluorine atoms,            -   wherein said methoxy and ethoxy are optionally                substituted with up to three fluorine atoms,        -   wherein said 2-oxopyridin-1(2H)-yl is optionally            substituted, identically or differently, with one or two            groups selected from fluorine, cyano, methyl, ethyl, methoxy            and ethoxy,            -   wherein said methyl and ethyl are optionally substituted                with up to three fluorine atoms,            -   wherein said methoxy and ethoxy are optionally                substituted with up to three fluorine atoms,        -   wherein said 6- to 8-membered heterocycle is optionally            substituted, identically or differently, with one or two            groups selected from (C₁-C₄)-alkyl, cyano,            (C₁-C₄)-alkoxycarbonyl and optionally up to five fluorine            atoms,            -   wherein said (C₁-C₄)-alkyl is optionally substituted                with up to three fluorine atoms,        -   wherein said (C₅-C₈)-cycloalkyl is optionally substituted,            identically or differently, with one or two groups selected            from (C₁-C₄)-alkyl and cyano, and optionally up to five            fluorine atoms,            -   wherein said (C₁-C₄)-alkyl is optionally substituted                with up to three fluorine atoms,

    -   R⁷ represents a hydrogen atom, (C₁-C₄)-alkyl, methylsulfonyl or        ethylsulfonyl,        -   wherein said (C₁-C₄)-alkyl is optionally substituted with a            group selected from (C₃-C₆)-cycloalkyl, hydroxy, —NR²⁰R²¹,            methoxy, ethoxy or benzyloxy and optionally with up to five            fluorine atoms,            -   wherein said (C₃-C₆)-cycloalkyl is optionally                substituted with hydroxy and optionally up to four                fluorine atoms,            -   and            -   wherein            -   R²⁰ represents a hydrogen atom or (C₁-C₄)-alkyl,            -   R²¹ represents a hydrogen atom or (C₁-C₄)-alkyl,

    -   with the proviso that if R⁵ is methoxy or ethoxy then R⁷ is        different from hydrogen,

    -   with the proviso that if R⁶ is pyridyl or pyrimidyl then R⁷ is        different from hydrogen,

    -   with the proviso that if R⁶ is 2-oxopyridin-1(2H)-yl then R⁷ is        different from hydrogen,

    -   with the proviso that if R⁶ is a 6- to 8-membered heterocycle        then R⁷ is different from hydrogen,

    -   R⁸ represents a group selected from fluorine, chlorine, cyano,        (C₁-C₄)-alkyl, methoxy, ethoxy, methylcarbonyl, ethylcarbonyl        and (C₃-C₅)-cycloalkyl,        -   wherein said (C₁-C₄)-alkyl is optionally substituted with            methoxy, —NR²²R²³ and cyclopropyl and optionally up to five            fluorine atoms,            -   wherein said cyclopropyl is optionally substituted with                up to four fluorine atoms            -   wherein said methoxy is optionally substituted with up                to three fluorine atoms,            -   wherein            -   R²² represents a hydrogen atom or (C₁-C₄)-alkyl,            -   R²³ represents a hydrogen atom or (C₁-C₄)-alkyl,            -   or            -   R²² and R²³ together with the nitrogen atom they are                attached form a 4- to 6-membered heterocycle                -   wherein said 4- to 6-membered heterocycle is                    optionally substituted, identically or differently,                    with one, two or three groups selected from                    (C₁-C₄)-alkyl and optionally up to five fluorine                    atoms,        -   wherein said methoxy and ethoxy are optionally substituted            with up to three fluorine atoms, and        -   wherein said (C₃-C₅)-cycloalkyl is optionally substituted            with up to four fluorine atoms,

    -   R⁹ represents pyridyl, pyrimidyl, 2-oxopyridin-1(2H)-yl,        (C₅-C₈)-cycloalkyl or a 6- to 8-membered heterocycle or        (C₁-C₄)-alkyl,        -   or        -   represents a group of the formula

-   -   -   in which        -   ## represents the point of attachment to the pyrazole ring,        -   R^(38b) represents a hydrogen atom, halogen or methyl,        -   R^(38c) represents a hydrogen atom, halogen or methyl,        -   R^(39b) represents a hydrogen atom, cyano, fluorine or            (C₁-C₄)-alkylsulfanyl,        -   R^(39c) represents a hydrogen atom, cyano, fluorine or            (C₁-C₄)-alkylsulfanyl,        -   R^(40a) represents a hydrogen atom, fluorine, chlorine,            cyano, hydroxy, —(CH₂)_(n)NR^(16a)R^(17a), (C₁-C₃)-alkyl,            (C₁-C₃)-alkoxy, (C₁-C₄)-alkoxycarbonyl, a 4- to 6-membered            heterocycle, cyclopropyl or cyclobutyl,            -   wherein said (C₁-C₃)-alkyl is optionally substituted                with cyano and optionally with up to five fluorine                atoms,            -   wherein said (C₁-C₃)-alkoxy is optionally substituted                with up to five fluorine atoms,            -   wherein said 4- to 6-membered heterocycle is optionally                substituted, identically or differently, with one, two                or three groups selected from (C₁-C₄)-alkyl and                optionally up to five fluorine atoms,            -   wherein            -   n represents 0 or 1,            -   R^(16a) represents a hydrogen atom or (C₁-C₄)-alkyl,            -   R^(17a) represents a hydrogen atom or (C₁-C₄)-alkyl,            -   or            -   R^(16a) and R^(17a) together with the nitrogen atom they                are attached form a 4- to 6-membered heterocycle                -   wherein said 4- to 6-membered heterocycle is                    optionally substituted, identically or differently,                    with one, two or three groups selected from                    (C₁-C₄)-alkyl and optionally up to five fluorine                    atoms,        -   wherein said (C₁-C₄)-alkyl is optionally substituted with up            to five fluorine atoms,        -   wherein said pyridyl and pyrimidyl are optionally            substituted, identically or differently, with one or two            groups selected from a halogen atom, cyano, methyl, ethyl,            methoxy and ethoxy,            -   wherein said methyl and ethyl is optionally substituted                with up to three fluorine atoms,            -   wherein said methoxy and ethoxy are optionally                substituted with up to three fluorine atoms,        -   wherein said 2-oxopyridin-1(2H)-yl is optionally            substituted, identically or differently, with one or two            groups selected from fluorine, cyano, methyl, ethyl, methoxy            and ethoxy,            -   wherein said methyl and ethyl are optionally substituted                with up to three fluorine atoms,            -   wherein said methoxy and ethoxy are optionally                substituted with up to three fluorine atoms,        -   wherein said 6- to 8-membered heterocycle is optionally            substituted, identically or differently, with one or two            groups selected from methyl, ethyl, cyano and            (C₁-C₄)-alkoxycarbonyl and optionally up to five fluorine            atoms,            -   wherein said methyl is optionally substituted with up to                three fluorine atoms,        -   wherein said (C₅-C₈)-cycloalkyl is optionally substituted,            identically or differently, with one or two groups selected            from methyl, ethyl and cyano, and optionally up to five            fluorine atoms,            -   wherein said methyl is optionally substituted with up to                three fluorine atoms,

    -   R¹⁰ represents a hydrogen atom, (C₁-C₄)-alkyl or        (C₃-C₅)-cycloalkyl,        -   wherein said (C₁-C₄)-alkyl is optionally substituted with a            group selected from (C₃-C₆)-cycloalkyl,            2-methyl-2H-tetrazol-5-yl, 1-methyl-1H-tetrazol-5-yl,            —NR²⁸R²⁹, methoxy, ethoxy or benzyloxy and optionally with            up to five fluorine atoms optionally with up to five            fluorine atoms and is optionally additionally substituted            with hydroxy,            -   wherein said (C₃-C₆)-cycloalkyl is optionally                substituted with up to four fluorine atoms,            -   and            -   wherein            -   R²⁸ represents a hydrogen atom or (C₁-C₄)-alkyl,            -   R²⁹ represents a hydrogen atom or (C₁-C₄)-alkyl,

    -   with the proviso that if R⁹ is pyridyl or pyrimidyl then R¹⁰ is        different from hydrogen,

    -   with the proviso that if R⁹ is 2-oxopyridin-1(2H)-yl then R¹⁰ is        different from hydrogen,

    -   with the proviso that if R⁹ is a 6- to 8-membered heterocycle        then R¹⁰ is different from hydrogen,

    -   with the proviso that if R⁸ is methoxy or ethoxy then R¹⁰ is        different from hydrogen,

    -   R¹¹ represents a group selected from a hydrogen atom,        (C₁-C₄)-alkyl and cyclopropyl,        -   wherein said (C₁-C₄)-alkyl is optionally substituted with            cyclopropyl and optionally with up to five fluorine atoms,

    -   R¹² represents pyridyl or 2-oxopyridin-1(2H)-yl,        -   or        -   represents a group of the formula

-   -   -   in which        -   ## represents the point of attachment to the pyrazole ring,        -   R^(38d) represents a hydrogen atom, fluorine or methyl,        -   R^(38e) represents a hydrogen atom, fluorine or methyl,        -   R^(39d) represents a hydrogen atom, cyano or fluorine,        -   R^(39e) represents a hydrogen atom,        -   R^(40b) represents a hydrogen atom, fluorine, chlorine,            cyano, hydroxy, methyl, trifluoromethyl, methoxy,            trifluoromethoxy or methoxycarbonyl,        -   wherein said pyridyl is optionally substituted, identically            or differently, with one or two groups selected from            fluorine, cyano, methyl and methoxy,            -   wherein said methyl is optionally substituted with up to                three fluorine atoms,            -   wherein said methoxy is optionally substituted with up                to three fluorine atoms,        -   wherein said 2-oxopyridin-1(2H)-yl is optionally            substituted, identically or differently, with one or two            groups selected from fluorine, cyano, methyl and methoxy,            -   wherein said methyl is optionally substituted with up to                three fluorine atoms,            -   wherein said methoxy is optionally substituted with up                to three fluorine atoms,

    -   R¹³ represents a group selected from a hydrogen atom,        (C₁-C₄)-alkyl and cyclopropyl,        -   wherein said (C₁-C₄)-alkyl is optionally substituted with            cyclopropyl and optionally with up to five fluorine atoms,

-   R² represents a group selected from a hydrogen atom, (C₁-C₄)-alkyl,    cyclopropyl, methoxycarbonyl and ethoxycarbonyl,    -   wherein said (C₁-C₄)-alkyl is optionally substituted,        identically or differently, with one or two groups selected from        hydroxy, methoxy, ethoxy, cyclopropyl and optionally up to five        fluorine atoms,

-   R³ represents a group selected from a hydrogen atom, fluorine,    chlorine, bromine, cyano, hydroxy, nitro, amino,    mono-(C₁-C₄)-alkylamino, di-(C₁-C₄)-alkylamino,    (C₁-C₄)-alkylsulfanyl, (C₁-C₄)-alkylsulfinyl, (C₁-C₄)-alkylsulfonyl,    (C₁-C₆)-alkyl, (C₁-C₄)-alkoxy, —O—C(═O)—NR³⁶R³⁷, —O—C(═O)—OR^(37a),    —NH—C(═O)—NR³⁶R³⁷, —N(CH₃)—C(═O)—NR³⁶R³⁷,    —NH—C(═O)—OR^(37a)—N(CH₃)—C(═O)—OR^(37a)—NH—C(═O)—R³⁷,    —N(CH₃)—C(═O)—R³⁷, (C₃-C₅)-cycloalkyl, 4- to 6-membered heterocycle,    5- to 6-membered heteroaryl, —(CH₂)_(q)—C(═O)—NR³⁴R³⁵,    methylcarbonyl, ethylcarbonyl, (C₁-C₄)-alkylcarbonyloxy and    (C₁-C₄)-alkoxycarbonyl,

wherein said (C₁-C₆)-alkyl is optionally substituted, identically ordifferently, with one or two groups selected from hydroxy, amino,mono-(C₁-C₄)-alkylamino, di-(C₁-C₄)-alkylamino, cyano, methoxy, ethoxy,methoxycarbonyl, ethoxycarbony, 4- to 6-membered heterocycle andcyclopropyl and optionally up to five fluorine atoms,

-   -   wherein said 4- to 6-membered heterocycle is optionally        substituted with methyl, ethyl or cyclopropyl and optionally up        to two fluorine atoms,

wherein said (C₁-C₄)-alkoxy is optionally substituted with cyano,cyclopropyl and optionally up to five fluorine atoms,

wherein said (C₃-C₅)-cycloalkyl is optionally substituted with hydroxyl,methoxy, ethoxy and optionally up to four fluorine atoms,

wherein said 4- to 6-membered heterocycle is optionally substituted withhydroxyl, trifluoromethyl, methoxy, ethoxy and optionally up to fourfluorine atoms,

wherein said 5- to 6-membered heteroaryl is optionally substituted,identically or differently, with one or two groups selected from methyl,ethyl and methoxy and optionally up to four fluorine atoms,

wherein

q is 0,

R³⁴ represents a hydrogen atom or (C₁-C₄)-alkyl,

R³⁵ represents a hydrogen atom or (C₁-C₄)-alkyl,

or

R³⁴ and R³⁵ together with the nitrogen atom they are attached form a 4-to 7-membered heterocycle,

-   -   wherein said 4- to 7-membered heterocyclel ring is optionally        substituted, identically or differently, with one, two or three        groups selected from a fluorine atom, hydroxy, methyl, ethyl,        methoxy, ethoxy, cyclopropyl, difluoromethyl, trifluoromethyl        and trifluoromethoxy,

wherein

R³⁶ represents a hydrogen atom or methyl,

R³⁷ represents a hydrogen atom, methyl, difluoromethyl, trifluoromethylor cyclopropyl,

-   -   R^(37a) represents methyl, difluoromethyl, trifluoromethyl or        cyclopropyl,

with the proviso that if R³ is —(CH₂)_(q)C(═O)—NR³⁴R³⁵,—O—C(═O)—NR³⁶R³⁷, —O—C(═O)—OR^(37a), —N(CH₃)—C(═O)—NR³⁶R³⁷,—NH—C(═O)—OR^(37a), —NH—C(═O)—NR³⁶R³⁷, —N(CH₃)—C(═O)—OR^(37a),—NH—C(═O)—R³⁷ or —N(CH₃)—C(═O)—R³⁷, then R⁷ and R¹⁰ are different fromhydrogen,

with the proviso that if R³ is cyano then R² and R⁴ are different fromhydrogen,

with the proviso that if R³ is cyano then R⁶ and R⁹ are different from6-membered heteroaryl,

or

R² and R³ together with the carbon atoms they are attached form a 5- to6-membered carbocycle, a 5- to 7-membered azaheterocycle, a 5- to7-membered oxaheterocycle, a 5- to 6-membered heteroaryl group or aphenyl ring,

-   -   wherein said 5- to 7-membered azaheterocycle is optionally        substituted, identically or differently, with one or two groups        selected from oxo, methyl, ethyl, propyl, trifluoromethyl and        (C₁-C₄)-alkoxycarbonyl and optionally up to four fluorine atoms,    -   wherein said 5- to 7-membered oxaheterocycle is optionally        substituted, identically or differently, with one or two groups        selected from oxo, methyl, ethyl, trifluoromethyl and        (C₁-C₄)-alkoxycarbonyl and optionally up to four fluorine atoms,    -   wherein said 5- to 6-membered carbocycle is optionally        substituted, identically or differently, with one or two groups        selected from hydroxy, oxo, amino, mono-(C₁-C₄)-alkylamino,        di-(C₁-C₄)-alkylamino, methyl, ethyl, trifluoromethyl and        (C₁-C₄)-alkoxycarbonyl and optionally up to four fluorine atoms,    -   and    -   wherein any phenyl group and any 5- to 6-membered heteroaryl        group are each optionally substituted, identically or        differently, with one or two groups selected from fluorine,        chlorine, methyl, ethyl, trifluoromethyl, methxoy and        trifluoromethoxy,

with the proviso that if R² and R³ together with the carbon atoms theyare attached to form a 5- to 7-membered azaheterocycle with anon-substituted nitrogen atom which is not directly attached to thepyrazole, then R⁷ and R¹⁰ are different from hydrogen, with the provisothat if R⁷ and R¹⁰ are hydrogen then the nitrogen atom of the 5- to7-membered azaheterocycle formed by R² and R³ together with the carbonatoms they are attached to is substituted with methyl, ethyl or(C₁-C₄)-alkoxycarbonyl,

-   R⁴ represents a group selected from a hydrogen atom, (C₁-C₄)-alkyl,    cyclopropyl, methoxycarbonyl, ethoxycarbonyl and hydroxy,    -   wherein said (C₁-C₄)-alkyl is optionally substituted,        identically or differently, with one or two groups selected from        hydroxy, methoxy and cyclopropyl and optionally up to five        fluorine atoms,

or

R³ and R⁴ together with the carbon atoms they are attached form a 5- to6-membered carbocycle, a 5- to 7-membered heterocycle, a 5- to6-membered heteroaryl group or a phenyl ring,

-   -   wherein said 5- to 7-membered heterocycle is optionally        substituted, identically or differently, with one or two groups        selected from oxo, methyl, ethyl, propyl trifluoromethyl and        (C₁-C₄)-alkoxycarbonyl and optionally up to four fluorine atoms,    -   wherein said 5- to 6-membered carbocycle is optionally        substituted, identically or differently, with one or two groups        selected from oxo, hydroxyl, methyl, ethyl, trifluoromethyl and        (C₁-C₄)-alkoxycarbonyl and optionally up to four fluorine atoms,    -   and    -   wherein any phenyl group and any 5- to 6-membered heteroaryl        group are each optionally substituted, identically or        differently, with one or two groups selected from fluorine,        chlorine, methyl, ethyl, trifluoromethyl, methoxy and        trifluoromethoxy,

with the proviso that if R³ and R⁴ together with the carbon atoms theyare attached form a 5- to 7-membered heterocycle with a non-substitutednitrogen atom which is not directly attached to the pyrazole, then R⁷and R¹⁰ is different from hydrogen,

with the proviso that if R⁷ and R¹⁰ are hydrogen then the nitrogen atomof the 5- to 7-membered heterocycle formed by R³ and R⁴ together withthe carbon atoms they are attached to is substituted with methyl, ethylor (C₁-C₄)-alkoxycarbonyl,

or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or asalt thereof, or a mixture of same.

Preference is given to compounds of the formula (I) in which:

-   R¹ represents a group of the formula

-   -   in which    -   # represents the point of attachment to the amino group,    -   R⁵ represents a group selected from chlorine, (C₁-C₄)-alkyl,        methoxy, ethoxy and (C₃-C₅)-cycloalkyl,        -   wherein said (C₁-C₄)-alkyl is optionally substituted with a            group selected from methoxy, difluoromethoxy,            trifluoromethoxy, —NR¹⁴R¹⁵, cyclopropyl or optionally with            up to three fluorine atoms,        -   wherein        -   R¹⁴ represents (C₁-C₄)-alkyl,        -   R¹⁵ represents (C₁-C₄)-alkyl,        -   or        -   R¹⁴ and R¹⁵ together with the nitrogen atom they are            attached form a 4- to 6-membered heterocycle            -   wherein said 4- to 6-membered heterocycle is optionally                substituted with methyl or trifluoromethyl or optionally                with up to four fluorine atoms,        -   wherein said methoxy and ethoxy are optionally substituted            with up to three fluorine atoms,        -   wherein said (C₃-C₅)-cycloalkyl is optionally substituted            with up to four fluorine atoms,    -   R⁶ represents pyridyl or (C₅-C₈)-cycloalkyl,        -   or        -   represents a group of the formula

-   -   -   in which        -   ## represents the point of attachment to the pyrazole ring,        -   R³⁸ represents a hydrogen atom, methyl or fluorine,        -   R^(38a) represents a hydrogen atom,        -   R³⁹ represents a hydrogen atom, cyano or fluorine,        -   R^(39a) represents a hydrogen atom, cyano, fluorine or            methylsulfanyl,        -   R⁴⁰ represents a hydrogen atom, fluorine, chlorine, cyano,            hydroxy, —(CH₂)_(n)NR¹⁶R¹⁷, methyl, methoxy, ethoxy,            difluoromethoxy, trifluoromethoxy, methoxycarbonyl or            ethoxycarbonyl,            -   wherein said methyl is optionally substituted with cyano                or optionally with up to three fluorine atoms,            -   wherein            -   n represents 0,            -   R¹⁶ represents a hydrogen atom or (C₁-C₄)-alkyl,            -   R¹⁷ represents (C₁-C₄)-alkyl,        -   wherein said pyridyl is optionally substituted, identically            or differently, with one or two groups selected from            fluorine, cyano, methyl, methoxy and ethoxy,            -   wherein said methyl is optionally substituted with up to                three fluorine atoms,            -   wherein said methoxy is optionally substituted with up                to three fluorine atoms,        -   wherein said (C₅-C₈)-cycloalkyl is optionally substituted,            identically or differently, with one or two groups selected            from (C₁-C₄)-alkyl and cyano, or optionally with up to five            fluorine atoms,            -   wherein said (C₁-C₄)-alkyl is optionally substituted                with up to three fluorine atoms,

    -   R⁷ represents a hydrogen atom or (C₁-C₄)-alkyl,        -   wherein said (C₁-C₄)-alkyl is optionally substituted with            (C₃-C₆)-cycloalkyl, methoxy or ethoxy or optionally with up            to three fluorine atoms,

    -   with the proviso that if R⁵ is methoxy, ethoxy, difluoromethoxy        or trifluoromethoxy then R⁷ is different from hydrogen,

    -   with the proviso that if R⁶ is pyridyl then R⁷ is different from        hydrogen,

    -   R⁸ represents a group selected from chlorine, (C₁-C₄)-alkyl,        methoxy, ethoxy and (C₃-C₅)-cycloalkyl,        -   wherein said (C₁-C₄)-alkyl is optionally substituted with a            group selected from methoxy —NR²²R²³, cyclopropyl or            optionally with up to three fluorine atoms,            -   wherein said methoxy is optionally substituted with up                to three fluorine atoms,            -   wherein            -   R²² represents (C₁-C₄)-alkyl,            -   R²³ represents (C₁-C₄)-alkyl,        -   wherein said methoxy and ethoxy are optionally substituted            with up to three fluorine atoms,        -   and        -   wherein said (C₃-C₅)-cycloalkyl is optionally substituted            with up to four fluorine atoms,

    -   R⁹ represents pyridyl or (C₅-C₈)-cycloalkyl,        -   or        -   represents a group of the formula

-   -   -   in which        -   ## represents the point of attachment to the pyrazole ring,        -   R^(38b) represents a hydrogen atom, methyl or fluorine,        -   R^(38c) represents a hydrogen atom or fluorine,        -   R^(39b) represents a hydrogen atom, cyano or fluorine,        -   R^(39c) represents a hydrogen atom, cyano or fluorine,        -   R^(40a) represents a hydrogen atom, fluorine, chlorine,            cyano, hydroxy, —(CH₂)_(n)NR^(16a)R^(17a), methyl, methoxy,            ethoxy, difluoromethoxy, trifluoromethoxy, methoxycarbonyl            or ethoxycarbonyl, a 4- to 6-membered heterocycle,            cyclopropyl or cyclobutyl,            -   wherein said methyl is optionally substituted with cyano                or optionally with up to three fluorine atoms,            -   wherein            -   n represents 0,            -   R^(16a) represents a hydrogen atom,            -   R^(17a) represents (C₁-C₄)-alkyl,            -   wherein said 4- to 6-membered heterocycle is optionally                substituted, with methyl or optionally with up to five                fluorine atoms,        -   wherein said pyridyl is optionally substituted, identically            or differently, with one or two groups selected from            fluorine, cyano, methyl, methoxy and ethoxy,            -   wherein said methyl is optionally substituted with up to                three fluorine atoms,            -   wherein said methoxy and ethoxy are optionally                substituted with up to three fluorine atoms,        -   wherein said (C₅-C₈)-cycloalkyl is optionally substituted,            identically or differently, with one or two groups selected            from methyl, ethyl, cyano or optionally with up to five            fluorine atoms,            -   wherein said methyl is optionally substituted with up to                three fluorine atoms,        -   R¹⁰ represents a hydrogen atom, (C₁-C₄)-alkyl or            cyclopropyl, wherein said (C₁-C₄)-alkyl is optionally            substituted with a group selected from (C₃-C₆)-cycloalkyl,            methoxy, ethoxy, 2-methyl-2H-tetrazol-5-yl,            1-methyl-1H-tetrazol-5-yl, —NR²⁸R²⁹ or optionally with up to            three fluorine atoms and is optionally additionally            substituted with hydroxy,            -   wherein said (C₃-C₆)-cycloalkyl is optionally                substituted with up to four fluorine atoms,            -   and            -   wherein            -   R²⁸ represents a hydrogen atom or (C₁-C₄)-alkyl,            -   R²⁹ represents (C₁-C₄)-alkyl,

    -   with the proviso that if R⁹ is pyridyl then R¹⁰ is different        from hydrogen,

    -   with the proviso that if R⁸ is methoxy, ethoxy, difluoromethoxy        or trifluoromethoxy then R¹⁰ is different from hydrogen,

    -   R¹¹ represents cyclopropyl, methyl or ethyl,        -   wherein said methyl or ethyl are optionally substituted with            cyclopropyl or optionally with up to three fluorine atoms,

    -   R¹² represents a group of the formula

-   -   -   in which        -   ## represents the point of attachment to the pyrazole ring,        -   R^(38d) represents a hydrogen atom or fluorine,        -   R^(38e) represents a hydrogen atom,        -   R^(39d) represents a hydrogen atom or fluorine,        -   R^(39e) represents a hydrogen atom,        -   R^(40b) represents a hydrogen atom, fluorine, chlorine or            cyano,

    -   R¹³ represents a group selected from a hydrogen atom, methyl and        cyclopropyl,        -   wherein said methyl is optionally substituted with            cyclopropyl or optionally with up to three fluorine atoms,

-   R² represents a hydrogen atom or methyl,    -   wherein said methyl is optionally substituted with up to three        fluorine atoms,

-   R³ represents a group selected from a hydrogen atom, fluorine,    chlorine, bromine, cyano, hydroxy, nitro, amino,    mono-(C₁-C₄)-alkylamino, di-(C₁-C₄)-alkylamino, methylsulfanyl,    ethylsulfanyl, methylsulfinyl, ethylsulfinyl, methylsulfonyl,    ethylsulfonyl, —O—C(═O)—OR^(37a), —NH—C(═O)—NR³⁶R³⁷,    —N(CH₃)—C(═O)—NR³⁶R³⁷, —NH—C(═O)—OR^(37a), (C₁-C₄)-alkyl, methoxy,    ethoxy, (C₃-C₅)-cycloalkyl, 4- to 6-membered heterocycle, 5-membered    heteroaryl, —(CH₂)_(q)—C(═O)—NR³⁴R³⁵, methoxycarbonyl and    ethoxycarbonyl,    -   wherein said (C₁-C₄)-alkyl is optionally substituted,        identically or differently, with one or two groups selected from        hydroxy, cyano, methoxy, ethoxy, methoxycarbonyl,        ethoxycarbonyl, methylamino, ethylamino, dimethylamino,        diethylamino, a 4- to 6-membered heterocycle and cyclopropyl and        optionally up to three fluorine atoms,        -   wherein said 4- to 6-membered heterocycle is optionally            substituted with methyl, ethyl or cyclopropyl and optionally            up to two fluorine atoms,    -   wherein said methoxy and ethoxy are optionally substituted with        cyano, cyclopropyl or optionally up to three fluorine atoms,    -   wherein said (C₃-C₅)-cycloalkyl is optionally substituted with        hydroxy or optionally with up to four fluorine atoms,    -   wherein said 4- to 6-membered heterocycle is optionally        substituted with hydroxyl or trifluoromethyl or optionally with        up to four fluorine atoms,    -   wherein said 5-membered heteroaryl is optionally substituted,        identically or differently, with one or two groups selected from        methyl and methoxy    -   wherein    -   q is 0,    -   R³⁴ represents a hydrogen atom or (C₁-C₄)-alkyl,    -   R³⁵ represents (C₁-C₄)-alkyl,    -   or    -   R³⁴ and R³⁵ together with the nitrogen atom they are attached        form a 4- to 6-membered heterocycle ring        -   wherein said 4- to 6-membered heterocycle ring is optionally            substituted, identically or differently, with one or two            groups selected from a fluorine atom, methyl,            difluoromethyl, trifluoromethyl and trifluoromethoxy,    -   wherein    -   R³⁶ represents a hydrogen atom or methyl,    -   R³⁷ represents a hydrogen atom, methyl, difluoromethyl,        trifluoromethyl or cyclopropyl,    -   R^(37a) represents methyl, difluoromethyl, trifluoromethyl or        cyclopropyl,

with the proviso that if R³ is —(CH₂)_(q)C(═O)—NR³⁴R³⁵,—O—C(═O)—OR^(37a), —NH—C(═O)—NR³⁶R³⁷, —N(CH₃)—C(′O)—NR³⁶R³⁷ or—NH—C(═O)—OR^(37a), then R⁷ and R¹⁰ are different from hydrogen,

with the proviso that if R³ is cyano then R² and R⁴ are different fromhydrogen,

with the proviso that if R³ is cyano then R⁶ and R⁹ are different frompyridyl or pyrimidyl,

or

R² and R³ together with the carbon atoms they are attached form a 4- to6-membered carbocycle, a 5- to 6-membered azaheterocycle, a 5- to6-membered oxaheterocycle, a 6-membered heteroaryl group or a phenylring,

wherein said phenyl group is optionally substituted, identically ordifferently, with one or two groups selected from fluorine, chlorine,methyl, trifluoromethyl, methxoy and trifluoromethoxy,

wherein said 5- to 6-membered carbocycle is optionally substituted,identically or differently, with one or two groups selected fromhydroxy, oxo, methyl, ethyl, trifluoromethyl and (C₁-C₄)-alkoxycarbonylor optionally with up to four fluorine atoms,

wherein said 5- to 6-membered azaheterocycle is optionally substitutedwith oxo, methyl, ethyl, propyl, trifluoromethyl, tert.-butoxycarbonylor optionally with up to four fluorine atoms,

wherein said 5- to 6-membered oxaheterocycle is optionally substitutedwith oxo, methyl, ethyl, trifluoromethyl, methoxycarbonyl andethoxycarbonyl or optionally with up to four fluorine atoms,

with the proviso that if R² and R³ together with the carbon atoms theyare attached to form a 5- to 6-membered azaheterocycle with anon-substituted nitrogen atom which is not directly attached to thepyrazole, then R⁷ and R¹⁰ are different from hydrogen,

with the proviso that if R⁷ and R¹⁰ are hydrogen then the nitrogen atomof the 5- to 6-membered azaheterocycle formed by R² and R³ together withthe carbon atoms they are attached to is substituted with methyl, ethyl,methoxycarbonyl or ethoxycarbonyl,

-   R⁴ represents a group selected from a hydrogen atom, (C₁-C₄)-alkyl,    cyclopropyl, methoxycarbonyl, ethoxycarbonyl and hydroxy,    -   wherein said (C₁-C₄)-alkyl is optionally substituted with a        group selected from hydroxy, methoxy and cyclopropyl or        optionally with up to three fluorine atoms,

or

R³ and R⁴ together with the carbon atoms they are attached form a 5- to6-membered carbocycle, a 5- to 6-membered heterocycle, a 6-memberedheteroaryl group or a phenyl ring,

-   -   wherein said 5- to 6-membered heterocycle is optionally        substituted, identically or differently, with one or two groups        selected from oxo, methyl, ethyl, propyl, trifluoromethyl,        methoxycarbonyl, ethoxycarbonyl, tert.-butoxycarbonyl or        optionally with up to four fluorine atoms,    -   wherein said 5- to 6-membered carbocycle is optionally        substituted, identically or differently, with one or two groups        selected from oxo, hydroxy, methyl, ethyl, trifluoromethyl        methoxycarbonyl and ethoxycarbonyl or optionally with up to four        fluorine atoms,    -   and    -   wherein any phenyl group and any 6-membered heteroaryl group are        each optionally substituted, identically or differently, with        one or two groups selected from fluorine, chlorine, methyl,        ethyl, trifluoromethyl, methxoy and trifluoromethoxy, with the        proviso that if R³ and R⁴ together with the carbon atoms they        are attached form a 5- to 6-membered heterocycle with a        non-substituted nitrogen atom which is not directly attached to        the pyrazole, then R⁷ and R¹⁰ is different from hydrogen,

with the proviso that if R⁷ and R¹⁰ are hydrogen then the nitrogen atomof the 5- to 6-membered heterocycle formed by R³ and R⁴ together withthe carbon atoms they are attached to is substituted with methyl, ethyl,methoxycarbonyl or ethoxycarbonyl,

or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or asalt thereof, or a mixture of same.

Preference is given to compounds of the formula (I) in which:

-   R¹ represents a group of the formula

-   -   in which    -   # represents the point of attachment to the amino group,    -   R⁵ represents a group selected from chlorine, methyl, ethyl,        methoxy or cyclopropyl,        -   wherein said methyl and ethyl are optionally substituted            with methoxy or optionally with up to three fluorine atoms,        -   wherein said methoxy is optionally substituted with up to            three fluorine atoms,    -   R⁶ represents 5-fluoropyridin-2-yl,        6-trifluoromethylpyridin-3-yl or cyclohexyl,        -   or        -   represents a group of the formula

-   -   -   in which        -   ## represents the point of attachment to the pyrazole ring,        -   R³⁸ represents a hydrogen atom or fluorine,        -   R^(38a) represents a hydrogen atom,        -   R³⁹ represents a hydrogen atom,        -   R^(39a) represents a hydrogen atom or cyano,        -   R⁴⁰ represents a hydrogen atom, fluorine, chlorine, cyano,            methyl, difluoromethyl, trifluoromethyl, methoxy, ethoxy,            difluoromethoxy, trifluoromethoxy, methoxycarbonyl or            ethoxycarbonyl,

    -   R⁷ represents a hydrogen atom, methyl, ethyl, cyclopropylmethyl,        2-cyclopropylethyl or 2,2-difluoroethyl,

    -   with the proviso that if R⁵ is methoxy, difluoromethoxy or        trifluoromethoxy then R⁷ is different from hydrogen,

    -   with the proviso that if R⁶ is 2-pyridinyl then R⁷ is different        from hydrogen,

    -   R⁸ represents a group selected from chlorine, methyl, ethyl,        methoxy and cylcopropyl,

    -   R⁹ represents pyridyl or        4-cyanopentacyclo[4.2.0.0^(2,5).0^(3,8).0^(4,7)]octan-1-yl,        -   or        -   represents a group of the formula

-   -   -   in which        -   ## represents the point of attachment to the pyrazole ring,        -   R^(38b) represents a hydrogen atom or fluorine,        -   R^(38c) represents a hydrogen atom,        -   R^(39b) represents a hydrogen atom,        -   R^(39c) represents a hydrogen atom,        -   R^(40a) represents a hydrogen atom, fluorine, chlorine,            cyano, methyl, difluoromethyl, trifluoromethyl, methylamino,            methoxy, difluoromethoxy, trifluoromethoxy or cyclopropyl,        -   wherein said pyridyl is optionally substituted with            fluorine, methyl, difluoromethyl, trifluoromethyl or            methoxy,

    -   R¹⁰ represents a hydrogen atom, methyl, ethyl,        2,2-difluoroethyl, cyclopropylmethyl, cyclobutylmethyl,        2-cyclopropylethyl, 2-cyclopropyl-2-hydroxypropyl,        2-cyclopropyl-2-hydroxyethyl, 2-methoxyethyl, or cyclopropyl,        -   wherein said methyl and ethyl are optionally substituted            with a group selected from cyclopropyl, methoxy or            optionally up to three fluorine atoms and is optionally            additionally substituted with hydroxy,

    -   with the proviso that if R⁹ is pyridyl then R¹⁰ is different        from hydrogen,

    -   with the proviso that if R⁸ is methoxy then R¹⁰ is different        from hydrogen,

    -   R¹¹ represents methyl,

    -   R¹² represents a group of the formula

-   -   -   in which        -   ## represents the point of attachment to the pyrazole ring,        -   R^(38d) represents a hydrogen atom,        -   R^(38e) represents a hydrogen atom,        -   R^(39d) represents a hydrogen atom,        -   R^(39e) represents a hydrogen atom,        -   R^(40b) represents fluorine or cyano,

    -   R¹³ represents a group selected from a hydrogen atom or methyl,

-   R² represents a hydrogen atom, methyl or difluoromethyl,

-   R³ represents a group selected from a hydrogen atom, fluorine,    chlorine, bromine, cyano, hydroxy, nitro, amino, ethylamino,    dimethylamino, —O—C(═O)—NR³⁶R³⁷, —O—C(═O)—OR^(37a),    —NH—C(═O)—OR^(37a), (C₁-C₄)-alkyl, methoxy, cyclopropyl, cyclobutyl,    4-membered heterocycle, 1,3,4-oxadiazol-2-yl,    2-(trifluoromethyl)-1,3-dioxolan-2-yl, —(CH₂)_(q)—C(═O)—NR³⁴R³⁵,    methoxycarbonyl and ethoxycarbonyl,    -   wherein said (C₁-C₄)-alkyl is optionally substituted,        identically or differently, with one or two groups selected from        hydroxy, methoxy, methoxycarbonyl, ethoxycarbonyl,        dimethylamino, a 4-membered azaheterocycle and cyclopropyl and        optionally up to three fluorine atoms,        -   wherein said 4-membered azaheterocycle is optionally            substituted with up to two fluorine atoms,    -   wherein said methoxy is optionally substituted with cyano,        cyclopropyl and optionally up to three fluorine atoms,    -   wherein said cyclopropyl and cyclobutyl are optionally        substituted with hydroxy,    -   wherein said 4-membered heterocycle is optionally substituted        with hydroxy,    -   wherein said 1,3,4-oxadiazol-2-yl is optionally substituted with        methyl,    -   wherein    -   q is 0,    -   R³⁴ represents methyl,    -   R³⁵ represents methyl,    -   or    -   R³⁴ and R³⁵ together with the nitrogen atom they are attached        form a 4- to 6-membered heterocycle ring        -   wherein said 4- to 6-membered heterocycle ring is optionally            substituted, identically or differently, with one or two            groups selected from a fluorine atom, methyl, difluoromethyl            and trifluoromethyl,    -   wherein    -   R³⁶ represents a methyl atom,    -   R³⁷ represents a hydrogen atom or methyl,    -   R^(37a) represents methyl,

with the proviso that if R³ is —(CH₂)_(q)C(═O)—NR³⁴R³⁵ O—C(═O)—NR³⁶R³⁷,—O—C(═O)—OR^(37a) or —NH—C(═O)—OR^(37a), then R⁷ and R¹⁰ are differentfrom hydrogen,

with the proviso that if R³ is cyano then R² and R⁴ are different fromhydrogen,

with the proviso that if R³ is cyano then R⁶ and R⁹ are different frompyridyl,

or

R² and R³ together with the carbon atoms they are attached form a 5- to6-membered carbocycle, a pyrrolidinyl, a pyridyl or a phenyl ring,

wherein said 5- to 6-membered carbocycle is optionally substituted,identically or differently, with one or two groups selected from oxo,methyl, trifluoromethyl and hydroxy,

wherein said pyrrolidinyl is substituted with propyl ortert.-butoxycarbonyl,

-   R⁴ represents a group selected from a hydrogen atom, methyl,    2-hydroxypropan-2-yl, fluoromethyl, difluoromethyl, methoxycarbonyl,    ethoxycarbonyl and hydroxy,

or

R³ and R⁴ together with the carbon atoms they are attached form a 5- to6-membered carbocycle, a pyrrolidinyl ring or a piperidinyl ring, apyridyl group or a phenyl ring,

-   -   wherein said pyrrolidinyl ring is substituted with propyl or        tert-butoxycarbonyl,    -   wherein said piperidinyl ring is substituted with propyl or        tert-butoxycarbonyl,    -   wherein said 5- to 6-membered carbocycle is optionally        substituted, identically or differently, with one or two groups        selected from oxo, hydroxy and methyl,

or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or asalt thereof, or a mixture of same.

Preference is also given to compounds of the formula (I) in which

R¹ represents a group of the formula

in which

# represents the point of attachment to the amino group,

R⁵ represents a group selected from a halogen atom, cyano,(C₁-C₄)-alkyl, (C₁-C₄)-alkoxy, (C₃-C₆)-cycloalkyl, 3- to 6-memberedheterocycle and (C₁-C₄)-alkylcarbonyl,

wherein said (C₁-C₄)-alkyl is optionally substituted, identically ordifferently, with one or two groups selected from hydroxy, —NR¹⁴R¹⁵,(C₁-C₄)-alkoxy and cyclopropyl and optionally up to five fluorine atoms,

-   -   wherein said cyclopropyl is optionally substituted with up to        four fluorine atoms,

wherein

R¹⁴ represents a hydrogen atom or (C₁-C₄)-alkyl,

R¹⁵ represents a hydrogen atom or (C₁-C₄)-alkyl,

or

R¹⁴ and R¹⁵ together with the nitrogen atom they are attached form a 3-to 6-membered heterocycle

wherein said 3- to 6-membered heterocycle is optionally substituted,identically or differently, with one, two or three groups selected from(C₁-C₄)-alkyl and optionally up to five fluorine atoms,

wherein said 3- to 6-membered heterocycle is optionally substituted,identically or differently, with one or two groups selected from(C₁-C₄)-alkyl and up to five fluorine atoms,

wherein said 3- to 6-membered heterocycle is optionally substituted,identically or differently, with one or two groups selected from(C₁-C₄)-alkyl and optionally up to five fluorine atoms,

wherein said (C₃-C₆)-cycloalkyl is optionally substituted, identicallyor differently, with one or two groups selected from (C₁-C₄)-alkyl andoptionally up to five fluorine atoms,

R⁶ represents a phenyl group or (C₄-C₆)-cycloalkyl,

wherein said phenyl group is optionally substituted, identically ordifferently, with one, two or three groups selected from a halogen atom,cyano, hydroxy, —(CH₂)_(n)NR¹⁶R¹⁷, (C₁-C₄)-alkyl, (C₁-C₄)-alkoxy,(C₁-C₄)-alkoxycarbonyl and —C(═O)—NR¹⁸R¹⁹,

wherein said (C₁-C₄)-alkyl is optionally substituted with cyano andoptionally with up to five fluorine atoms,

wherein said (C₁-C₄)-alkoxy is optionally substituted with up to fivefluorine atoms, wherein

n represents 0 or 1,

R¹⁶ represents a hydrogen atom or (C₁-C₄)-alkyl,

wherein said (C₁-C₄)-alkyl is optionally substituted with up to fivefluorine atoms,

R¹⁷ represents a hydrogen atom or (C₁-C₄)-alkyl,

wherein said (C₁-C₄)-alkyl is optionally substituted with up to fivefluorine atoms,

or

R¹⁶ and R¹⁷ together with the nitrogen atom they are attached form a 3-to 8-membered heterocycle

wherein said 3- to 8-membered heterocycle is optionally substituted,identically or differently, with one, two or three groups selected from(C₁-C₄)-alkyl and optionally up to five fluorine atoms,

wherein

R¹⁸ represents a hydrogen atom or (C₁-C₄)-alkyl,

R¹⁹ represents a hydrogen atom or (C₁-C₄)-alkyl,

or

R¹⁸ and R¹⁹ together with the nitrogen atom they are attached form a 3-to 8-membered heterocycle

wherein said 3- to 8-membered heterocycle is optionally substituted,identically or differently, with one, two or three groups selected from(C₁-C₄)-alkyl and optionally up to five fluorine atoms,

wherein said (C₄-C₆)-cycloalkyl is optionally substituted, identicallyor differently, with one or two groups selected from (C₁-C₄)-alkyl andoptionally up to five fluorine atoms,

wherein said (C₁-C₄)-alkyl is optionally substitutedwith(C₃-C₆)-cycloalkyl and optionally up to five fluorine atoms,

R⁷ represents a hydrogen atom, (C₁-C₄)-alkyl, a phenyl group, a 5- to6-membered heteroaryl group or (C₁-C₄)-alkylsulfonyl,

wherein any phenyl group and any 5- to 6-membered heteroaryl are eachoptionally substituted, identically or differently, with one, two orthree groups selected from a halogen atom, (C₁-C₄)-alkyl,trifluoromethyl, (C₁-C₄)-alkoxy and trifluoromethoxy,

wherein said (C₁-C₄)-alkyl is optionally substituted with a groupselected from(C₃-C₆)-cycloalkyl, 4- to 6-membered heterocycle, —NR²⁰R²¹,(C₁-C₄)-alkoxy or benzyloxy and optionally with up to five fluorineatoms,

wherein said (C₃-C₆)-cycloalkyl is optionally substituted, identicallyor differently, with one or two groups selected from (C₁-C₄)-alkyl andup to five fluorine atoms,

wherein said 4- to 6-membered heterocycle is optionally substituted,identically or differently, with one or two groups selected from(C₁-C₄)-alkyl and optionally up to five fluorine atoms,

and

wherein

R²⁰ represents a hydrogen atom or (C₁-C₄)-alkyl,

R²¹ represents a hydrogen atom or (C₁-C₄)-alkyl,

or

R²⁰ and R²¹ together with the nitrogen atom they are attached form a 3-to 6-membered heterocycle

wherein said 3- to 6-membered heterocycle is optionally substituted,identically or differently, with one, two or three groups selected from(C₁-C₄)-alkyl and optionally up to five fluorine atoms,

R⁸ represents a group selected from a halogen atom, cyano,(C₁-C₄)-alkyl, (C₃-C₆)-cycloalkyl, 3- to 6-membered heterocycle,(C₁-C₄)-alkylcarbonyl and a phenyl group,

wherein said (C₁-C₄)-alkyl is optionally substituted, identically ordifferently, with one or two groups selected from hydroxy, —NR²²R²³(C₁-C₄)-alkoxy and cyclopropyl and optionally up to five fluorine atoms,

-   -   wherein said cyclopropyl is optionally substituted with up to        four fluorine atoms

wherein

R²² represents a hydrogen atom or (C₁-C₄)-alkyl,

R²³ represents a hydrogen atom or (C₁-C₄)-alkyl,

or

R²² and R²³ together with the nitrogen atom they are attached form a 3-to 6-membered heterocycle

wherein said 3- to 6-membered heterocycle is optionally substituted,identically or differently, with one, two or three groups selected from(C₁-C₄)-alkyl and optionally up to five fluorine atoms,

wherein said (C₃-C₆)-cycloalkyl is optionally substituted, identicallyor differently, with one or two groups selected from (C₁-C₄)-alkyl andoptionally up to five fluorine atoms,

wherein said 3- to 6-membered heterocycle is optionally substituted,identically or differently, with one or two groups selected from(C₁-C₄)-alkyl and optionally up to five fluorine atoms,

and

wherein said phenyl group is optionally substituted, identically ordifferently, with one, two or three groups selected from a halogen atom,cyano, (C₁-C₄)-alkyl, trifluoromethyl, (C₁-C₄)-alkoxy andtrifluoromethoxy,

R⁹ represents a phenyl group, (C₄-C₆)-cycloalkyl or (C₁-C₄)-alkyl,

wherein said (C₁-C₄)-alkyl is optionally substituted with up to fivefluorine atoms,

wherein said phenyl group is optionally substituted, identically ordifferently, with one, two or three groups selected from a halogen atom,cyano, hydroxy, —(CH₂)_(m)NR²⁴R²⁵, (C₁-C₄)-alkyl, (C₁-C₄)-alkoxy,(C₁-C₄)-alkoxycarbonyl and —C(═O)—NR²⁶R²⁷,

wherein said (C₁-C₄)-alkyl is optionally substituted with cyano andoptionally with up to five fluorine atoms,

wherein said (C₁-C₄)-alkoxy is optionally substituted with up to fivefluorine atoms,

wherein

m represents 0 or 1,

R²⁴ represents a hydrogen atom or (C₁-C₄)-alkyl,

wherein said (C₁-C₄)-alkyl is optionally substituted with up to fivefluorine atoms,

R²⁵ represents a hydrogen atom or (C₁-C₄)-alkyl,

wherein said (C₁-C₄)-alkyl is optionally substituted with up to fivefluorine atoms,

or

R²⁴ and R²⁵ together with the nitrogen atom they are attached form a 3-to 6-membered heterocycle

wherein said 3- to 6-membered heterocycle is optionally substituted,identically or differently, with one, two or three groups selected from(C₁-C₄)-alkyl and optionally up to five fluorine atoms,

wherein

R²⁶ represents a hydrogen atom or (C₁-C₄)-alkyl,

R²⁷ represents a hydrogen atom or (C₁-C₄)-alkyl,

or

R²⁶ and R²⁷ together with the nitrogen atom they are attached form a 3-to 8-membered heterocycle wherein said 3- to 8-membered heterocycle isoptionally substituted, identically or differently, with one, two orthree groups selected from (C₁-C₄)-alkyl and optionally up to fivefluorine atoms,

wherein said (C₄-C₆)-cycloalkyl is optionally substituted, identicallyor differently, with one or two groups selected from (C₁-C₄)-alkyl andoptionally up to five fluorine atoms,

wherein said (C₁-C₄)-alkyl is optionally substituted with(C₃-C₆)-cycloalkyl and optionally up to five fluorine atoms,

R¹⁰ represents a hydrogen atom, (C₁-C₄)-alkyl, (C₃-05)-cycloalkyl aphenyl group or a 5- to 6-membered heteroaryl group,

wherein any phenyl group and any 5- to 6-membered heteroaryl are eachoptionally substituted, identically or differently, with one, two orthree groups selected from a halogen atom, (C₁-C₄)-alkyl,trifluoromethyl, (C₁-C₄)-alkoxy and trifluoromethoxy,

wherein said (C₁-C₄)-alkyl is optionally substituted with a groupselected from(C₃-C₆)-cycloalkyl, 3- to 6-membered heterocycle, —NR²⁸R²⁹,(C₁-C₄)-alkoxy or benzyloxy and optionally with up to five fluorineatoms,

wherein said (C₃-C₆)-cycloalkyl is optionally substituted, identicallyor differently, with one or two groups selected from (C₁-C₄)-alkyl andoptionally up to five fluorine atoms,

wherein said 3- to 6-membered heterocycle is optionally substituted,identically or differently, with one or two groups selected from(C₁-C₄)-alkyl and optionally up to five fluorine atoms,

and

wherein

R²⁸ represents a hydrogen atom or (C₁-C₄)-alkyl,

R²⁹ represents a hydrogen atom or (C₁-C₄)-alkyl,

or

R²⁸ and R²⁹ together with the nitrogen atom they are attached form a 3-to 6-membered heterocycle

wherein said 3- to 6-membered heterocycle is optionally substituted,identically or differently, with one, two or three groups selected from(C₁-C₄)-alkyl and optionally up to five fluorine atoms,

R¹¹ represents a group selected from a hydrogen atom, a fluorine atom, achlorine atom, (C₁-C₄)-alkyl and cyclopropyl,

wherein said (C₁-C₄)-alkyl is optionally substituted with up to fivefluorine atoms,

R¹² represents a phenyl group, a 5- to 6-membered heteroaryl group,(C₄-C₆)-cycloalkyl or (C₁-C₄)-alkyl,

wherein said phenyl group is optionally substituted, identically ordifferently, with one, two or three groups selected from a halogen atom,cyano, hydroxy, —(CH₂)_(p)NR³⁰R³¹, (C₁-C₄)-alkyl, trifluoromethyl,(C₁-C₄)-alkoxy, trifluoromethoxy, (C₁-C₄)-alkoxycarbonyl and—C(═O)—NR³²R³³,

wherein said (C₄-C₆)-cycloalkyl is optionally substituted, identicallyor differently, with one or two groups selected from (C₁-C₄)-alkyl andoptionally up to five fluorine atoms,

wherein

p represents 0 or 1,

R³⁰ represents a hydrogen atom or (C₁-C₄)-alkyl,

wherein said (C₁-C₄)-alkyl is optionally substituted with up to fivefluorine atoms,

R³¹ represents a hydrogen atom or (C₁-C₄)-alkyl,

wherein said (C₁-C₄)-alkyl is optionally substituted with up to fivefluorine atoms,

or

R³⁰ and R³¹ together with the nitrogen atom they are attached form a 3-to 6-membered heterocycle

wherein said 3- to 6-membered heterocycle is optionally substituted,identically or differently, with one, two or three groups selected from(C₁-C₄)-alkyl and optionally up to five fluorine atoms,

wherein

R³² represents a hydrogen atom or (C₁-C₄)-alkyl,

R³³ represents a hydrogen atom or (C₁-C₄)-alkyl,

or

R³² and R³³ together with the nitrogen atom they are attached form a 3-to 8-membered heterocycle

wherein said 3- to 8-membered heterocycle is optionally substituted,identically or differently, with one, two or three groups selected from(C₁-C₄)-alkyl and optionally up to five fluorine atoms,

R¹³ represents a group selected from a hydrogen atom, a fluorine atom, achlorine atom, (C₁-C₄)-alkyl and cyclopropyl,

wherein said (C₁-C₄)-alkyl is optionally substituted with up to fivefluorine atoms,

R² represents a group selected from a hydrogen atom, (C₁-C₄)-alkyl,(C₃-C₆)-cycloalkyl and (C₁-C₄)-alkoxycarbonyl,

wherein said (C₁-C₄)-alkyl is optionally substituted, identically ordifferently, with one or two groups selected from hydroxy,(C₁-C₄)-alkoxy, cyclopropyl and optionally up to five fluorine atoms,

R³ represents a group selected from a hydrogen atom, a halogen atom,cyano, (C₁-C₆)-alkyl, (C₃-C₆)-cycloalkyl, 3- to 6-membered heterocycle,5- to 6-membered heteroaryl, —(CH₂)_(q)C(═O)—NR³⁴R³⁵,(C₁-C₄)-alkylcarbonyl and (C₁-C₄)-alkoxycarbonyl,

wherein said (C₁-C₆)-alkyl is optionally substituted, identically ordifferently, with one or two groups selected from hydroxy, cyano,(C₁-C₄)-alkoxy, (C₁-C₄)-alkoxycarbonyl and cyclopropyl and optionally upto five fluorine atoms,

wherein said (C₃-C₆)-cycloalkyl is optionally substituted, identicallyor differently, with one or two groups selected from (C₁-C₄)-alkyl,(C₁-C₄)-alkoxy, and cyclopropyl and optionally up to five fluorineatoms,

wherein said 3- to 6-membered heterocycle is optionally substituted,identically or differently, with one or two groups selected from(C₁-C₄)-alkyl, (C₁-C₄)-alkoxy, and cyclopropyl and optionally up to fivefluorine atoms,

wherein said 5- to 6-membered heteroaryl is optionally substituted,identically or differently, with one or two groups selected from(C₁-C₄)-alkyl, (C₁-C₄)-alkoxy, and cyclopropyl and optionally up to fivefluorine atoms,

wherein

q represents 0 or 1,

R³⁴ represents a hydrogen atom or (C₁-C₄)-alkyl,

R³⁵ represents a hydrogen atom, (C₁-C₄)-alkyl or phenyl,

or

R³⁴ and R³⁵ together with the nitrogen atom they are attached form a 3-to 7-membered heterocyclyl ring

wherein said 3- to 7-membered heterocyclyl ring is optionallysubstituted, identically or differently, with one, two or three groupsselected from a fluorine atom, hydroxy, (C₁-C₄)-alkyl, (C₁-C₄)-alkoxy,cyclopropyl, difluoromethyl, trifluoromethyl and trifluoromethoxy,

or

R² and R³ together with the carbon atoms they are attached form a 4- to6-membered carbocycle, a 4- to 7-membered heterocycle, a 5- to6-membered heteroaryl group or a phenyl ring,

wherein said 4- to 7-membered heterocycle is optionally substituted,identically or differently, with one or two groups selected from afluorine atom, hydroxy, oxo, (C₁-C₄)-alkyl, trifluoromethyl,(C₁-C₄)-alkylcarbonyl and (C₁-C₄)-alkoxycarbonyl and optionally up tofive fluorine atoms,

wherein said 4- to 6-membered carbocycle is optionally substituted,identically or differently, with one or two groups selected from afluorine atom, hydroxy, oxo, (C₁-C₄)-alkyl, trifluoromethyl,(C₁-C₄)-alkylcarbonyl and (C₁-C₄)-alkoxycarbonyl and optionally up tofive fluorine atoms,

and

wherein any phenyl group and any 5- to 6-membered heteroaryl group areeach optionally substituted, identically or differently, with one, twoor three groups selected from a halogen atom, (C₁-C₄)-alkyl,trifluoromethyl, (C₁-C₄)-alkoxy and trifluoromethoxy,

R⁴ represents a group selected from a hydrogen atom, (C₁-C₄)-alkyl,(C₃-C₆)-cycloalkyl and (C₁-C₄)-alkoxycarbonyl and hydroxy,

wherein said (C₁-C₄)-alkyl is optionally substituted, identically ordifferently, with one or two groups selected from hydroxy,(C₁-C₄)-alkoxy and cyclopropyl and optionally up to five fluorine atoms,

or

R³ and R⁴ together with the carbon atoms they are attached form a a 4-to 6-membered carbocycle, a 4- to 7-membered heterocycle, a 5- to6-membered heteroaryl group or a phenyl ring,

wherein said 4- to 7-membered heterocycle is optionally substituted,identically or differently, with one or two groups selected from afluorine atom, hydroxy, oxo, (C₁-C₄)-alkyl, trifluoromethyl,(C₁-C₄)-alkylcarbonyl and (C₁-C₄)-alkoxycarbonyl and optionally up tofive fluorine atoms,

wherein said 4- to 6-membered carbocycle is optionally substituted,identically or differently, with one or two groups selected from afluorine atom, hydroxy, oxo, (C₁-C₄)-alkyl, trifluoromethyl,(C₁-C₄)-alkylcarbonyl and (C₁-C₄)-alkoxycarbonyl and optionally up tofive fluorine atoms,

and

wherein any phenyl group and any 5- to 6-membered heteroaryl group areeach optionally substituted, identically or differently, with one, twoor three groups selected from a halogen atom, (C₁-C₄)-alkyl,trifluoromethyl, (C₁-C₄)-alkoxy and trifluoromethoxy,

or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or asalt thereof, or a mixture of same.

Preference is also given to compounds of the formula (I) in which

R¹ represents a group of the formula

in which

# represents the point of attachment to the amino group,

R⁵ represents a group selected from fluorine, chlorine, cyano,(C₁-C₄)-alkyl, methoxy, ethoxy, (C₃-C₅)-cycloalkyl, 4- to 6-memberedheterocycle, methylcarbonyl and ethylcarbonyl,

wherein said (C₁-C₄)-alkyl is optionally substituted, identically ordifferently, with one or two groups selected from hydroxy, —NR¹⁴R¹⁵,methoxy, ethoxy and cyclopropyl and optionally up to five fluorineatoms,

-   -   wherein said cyclopropyl is optionally substituted with up to        four fluorine atoms,

wherein

R¹⁴ represents a hydrogen atom or (C₁-C₄)-alkyl,

R¹⁵ represents a hydrogen atom or (C₁-C₄)-alkyl,

or

R¹⁴ and R¹⁵ together with the nitrogen atom they are attached form a 3-to 6-membered heterocycle

wherein said 3- to 6-membered heterocycle is optionally substituted,identically or differently, with one, two or three groups selected from(C₁-C₄)-alkyl and optionally up to five fluorine atoms,

wherein said (C₃-C₅)-cycloalkyl is optionally substituted with up tofour fluorine atoms,

wherein said 4- to 6-membered heterocycle is optionally substituted upto four fluorine atoms,

R⁶ represents a phenyl group or cyclohexyl,

wherein said phenyl group is optionally substituted, identically ordifferently, with one, two or three groups selected from fluorine,chlorine, —(CH₂)_(r)CN, hydroxy, —NR¹⁶R¹⁷, (C₁-C₃)-alkyl,(C₁-C₃)-alkoxy, methoxycarbonyl, ethoxy carbonyl and —C(═O)—NR¹⁸R¹⁹,

wherein said (C₁-C₃)-alkyl is optionally substituted with up to threefluorine atoms,

wherein said (C₁-C₃)-alkoxy is optionally substituted with up to threefluorine atoms,

wherein

r represents 0 or 1,

R¹⁶ represents a hydrogen atom or (C₁-C₄)-alkyl,

R¹⁷ represents a hydrogen atom or (C₁-C₄)-alkyl,

or

R¹⁶ and R¹⁷ together with the nitrogen atom they are attached form a 3-to 6-membered heterocycle

wherein said 3- to 6-membered heterocycle is optionally substituted,identically or differently, with one, two or three groups selected from(C₁-C₄)-alkyl and optionally up to four fluorine atoms,

wherein

R¹⁸ represents a hydrogen atom or (C₁-C₄)-alkyl,

R¹⁹ represents a hydrogen atom or (C₁-C₄)-alkyl,

or

R¹⁸ and R¹⁹ together with the nitrogen atom they are attached form a 3-to 8-membered heterocycle

wherein said 3- to 8-membered heterocycle is optionally substituted,identically or differently, with one, two or three groups selected from(C₁-C₄)-alkyl and optionally up to four fluorine atoms,

wherein said cyclohexyl is optionally substituted, identically ordifferently, with one or two groups selected from (C₁-C₄)-alkyl andoptionally up to four fluorine atoms,

R⁷ represents a hydrogen atom, (C₁-C₄)-alkyl, (C₃-C₅)-cycloalkyl,methylsulfonyl or ethylsulfonyl,

wherein said (C₁-C₄)-alkyl is optionally substituted with a groupselected from (C₃-C₆)-cycloalkyl, 4- to 6-membered heterocycle,—NR²⁰R²¹, methoxy, ethoxy or benzyloxy and optionally with up to fivefluorine atoms,

wherein said (C₃-C₆)-cycloalkyl is optionally substituted with up tofour fluorine atoms,

wherein said 4- to 6-membered heterocycle is optionally substituted,identically or differently, with one or two groups selected from(C₁-C₄)-alkyl and optionally up to five fluorine atoms,

and

wherein

R²⁰ represents a hydrogen atom or (C₁-C₄)-alkyl,

R²¹ represents a hydrogen atom or (C₁-C₄)-alkyl,

or

R²⁰ and R²¹ together with the nitrogen atom they are attached form a 3-to 6-membered heterocycle

wherein said 3- to 6-membered heterocycle is optionally substituted,identically or differently, with one, two or three groups selected from(C₁-C₄)-alkyl and optionally up to five fluorine atoms,

R⁸ represents a group selected from fluorine, chlorine, cyano,(C₁-C₄)-alkyl, methoxy, ethoxy, (C₃-C₅)-cycloalkyl, 4- to 6-memberedheterocycle and a phenyl group,

wherein said (C₁-C₄)-alkyl is optionally substituted with hydroxy,methoxy, —NR²²R²³ and cyclopropyl and optionally up to five fluorineatoms,

-   -   wherein said cyclopropyl is optionally substituted with up to        four fluorine atoms

wherein

R²² represents a hydrogen atom or (C₁-C₄)-alkyl,

R²³ represents a hydrogen atom or (C₁-C₄)-alkyl,

or

R²² and R²³ together with the nitrogen atom they are attached form a 3-to 6-membered heterocycle

wherein said 3- to 6-membered heterocycle is optionally substituted,identically or differently, with one, two or three groups selected from(C₁-C₄)-alkyl and optionally up to five fluorine atoms,

wherein said (C₃-C₅)-cycloalkyl is optionally substituted with up tofour fluorine atoms,

wherein said 4- to 6-membered heterocycle is optionally substituted upto four fluorine atoms,

and

wherein said phenyl group is optionally substituted with fluorine,chlorine, cyano, methyl, trifluoromethyl, methoxy and trifluoromethoxy,

R⁹ represents a phenyl group, cyclohexyl or (C₁-C₄)-alkyl,

wherein said (C₁-C₄)-alkyl is optionally substituted with up to fivefluorine atoms,

wherein said phenyl group is optionally substituted, identically ordifferently, with one, two or three groups selected from fluorine,chlorine, (CH₂)_(t)CN, hydroxy, —NR²⁴R²⁵, (C₁-C₃)-alkyl, (C₁-C₃)-alkoxy,trifluoromethoxy, methoxycarbonyl, ethoxycarbonyl and —C(═O)—NR²⁶R²⁷,

-   -   wherein    -   t represents 0 or 1,    -   wherein said (C₁-C₃)-alkyl is optionally substituted with up to        three fluorine atoms,

wherein said (C₁-C₃)-alkoxy is optionally substituted with up to threefluorine atoms,

wherein

R²⁴ represents a hydrogen atom or (C₁-C₄)-alkyl,

R²⁵ represents a hydrogen atom or (C₁-C₄)-alkyl,

or

R²⁴ and R²⁵ together with the nitrogen atom they are attached form a 3-to 6-membered heterocycle

wherein said 3- to 6-membered heterocycle is optionally substituted,identically or differently, with one, two or three groups selected from(C₁-C₄)-alkyl and optionally up to five fluorine atoms,

wherein

R²⁶ represents a hydrogen atom or (C₁-C₄)-alkyl,

R²⁷ represents a hydrogen atom or (C₁-C₄)-alkyl,

or

R²⁶ and R²⁷ together with the nitrogen atom they are attached form a 3-to 5-membered heterocycle

wherein said 3- to 5-membered heterocycle is optionally substituted,identically or differently, with one, two or three groups selected from(C₁-C₄)-alkyl and optionally up to five fluorine atoms,

wherein said cyclohexyl is optionally substituted, identically ordifferently, with one or two groups selected from (C₁-C₄)-alkyl andoptionally up to five fluorine atoms,

R¹⁰ represents a hydrogen atom, (C₁-C₄)-alkyl or (C₃-C₅)-cycloalkyl,

wherein said (C₁-C₄)-alkyl is optionally substituted with a groupselected from(C₃-C₆)-cycloalkyl, 4- to 6-membered heterocycle, —NR²⁸R²⁹,methoxy, ethoxy or benzyloxy and optionally with up to five fluorineatoms,

wherein said (C₃-C₆)-cycloalkyl is optionally substituted with up tofour fluorine atoms,

wherein said 4- to 6-membered heterocycle is optionally substituted withup to four fluorine atoms,

and

wherein

R²⁸ represents a hydrogen atom or (C₁-C₄)-alkyl,

R²⁹ represents a hydrogen atom or (C₁-C₄)-alkyl,

or

R²⁸ and R²⁹ together with the nitrogen atom they are attached form a 3-to 6-membered heterocycle

wherein said 3- to 6-membered heterocycle is optionally substituted,identically or differently, with one, two or three groups selected from(C₁-C₄)-alkyl and optionally up to five fluorine atoms,

R¹¹ represents a group selected from a hydrogen atom, (C₁-C₄)-alkyl andcyclopropyl,

wherein said (C₁-C₄)-alkyl is optionally substituted with up to fivefluorine atoms,

R¹² represents a phenyl group,

wherein said phenyl group is optionally substituted, identically ordifferently, with one or two groups selected from fluorine, chlorine,cyano, methyl, trifluoromethyl, methoxy, trifluoromethoxy andmethoxycarbonyl,

R¹³ represents a group selected from a hydrogen atom, (C₁-C₄)-alkyl andcyclopropyl,

wherein said (C₁-C₄)-alkyl is optionally substituted with up to fivefluorine atoms,

R² represents a group selected from a hydrogen atom, (C₁-C₄)-alkyl,cyclopropyl, methoxycarbonyl and ethoxy carbonyl,

wherein said (C₁-C₄)-alkyl is optionally substituted, identically ordifferently, with one or two groups selected from hydroxy, methoxy,ethoxy, cyclopropyl and optionally up to five fluorine atoms,

R³ represents a group selected from a hydrogen atom, fluorine, chlorine,cyano, (C₁-C₆)-alkyl, (C₃-C₅)-cycloalkyl, 4- to 6-membered heterocycle,5- to 6-membered heteroaryl, —C(═O)—NR³⁴R³⁵, methylcarbonyl,ethylcarbonyl and (C₁-C₄)-alkoxycarbonyl,

wherein said (C₁-C₆)-alkyl is optionally substituted, identically ordifferently, with one or two groups selected from hydroxy, cyano,methoxy, ethoxy, methoxycarbonyl, ethoxycarbonyl and cyclopropyl andoptionally up to five fluorine atoms,

wherein said (C₃-C₆)-cycloalkyl is optionally substituted with up tofour fluorine atoms,

wherein said 3- to 6-membered heterocycle is optionally substituted withup to four fluorine atoms,

wherein said 5- to 6-membered heteroaryl is optionally substituted,identically or differently, with one or two groups selected from methyl,ethyl and methoxy and optionally up to four fluorine atoms,

wherein

R³⁴ represents a hydrogen atom or (C₁-C₄)-alkyl,

R³⁵ represents a hydrogen atom or (C₁-C₄)-alkyl,

or

R³⁴ and R³⁵ together with the nitrogen atom they are attached form a(C₃-C₇)-heterocyclyl ring

wherein said (C₃-C₇)-heterocyclyl ring is optionally substituted,identically or differently, with one, two or three groups selected froma fluorine atom, hydroxy, methyl, ethyl, methoxy, ethoxy, cyclopropyl,difluoromethyl, trifluoromethyl and trifluoromethoxy,

or

R² and R³ together with the carbon atoms they are attached form a 4- to6-membered carbocycle, a 4- to 7-membered heterocycle, a 5- to6-membered heteroaryl group or a phenyl ring,

wherein said 4- to 7-membered heterocycle is optionally substituted,identically or differently, with one or two groups selected from oxo,methyl, ethyl, trifluoromethyl and (C₁-C₄)-alkoxycarbonyl and optionallyup to four fluorine atoms,

wherein said 4- to 6-membered carbocycle is optionally substituted,identically or differently, with one or two groups selected from oxo,methyl, ethyl, trifluoromethyl and (C₁-C₄)-alkoxycarbonyl and optionallyup to four fluorine atoms,

and

wherein any phenyl group and any 5- to 6-membered heteroaryl group areeach optionally substituted, identically or differently, with one or twogroups selected from fluorine, chlorine, methyl, ethyl, trifluoromethyl,methxoy and trifluoromethoxy,

R⁴ represents a group selected from a hydrogen atom, (C₁-C₄)-alkyl,cyclopropyl, methoxycarbonyl, ethoxycarbonyl and hydroxy,

wherein said (C₁-C₄)-alkyl is optionally substituted, identically ordifferently, with one or two groups selected from hydroxy, methoxy andcyclopropyl and optionally up to five fluorine atoms,

or

R³ and R⁴ together with the carbon atoms they are attached form a 4- to6-membered carbocycle, a 4- to 7-membered heterocycle, a 5- to6-membered heteroaryl group or a phenyl ring,

wherein said 4- to 7-membered heterocycle is optionally substituted,identically or differently, with one or two groups selected from oxo,methyl, ethyl, trifluoromethyl and (C₁-C₄)-alkoxycarbonyl and optionallyup to four fluorine atoms,

wherein said 4- to 6-membered carbocycle is optionally substituted,identically or differently, with one or two groups selected from oxo,hydroxyl, methyl, ethyl, trifluoromethyl and (C₁-C₄)-alkoxycarbonyl andoptionally up to four fluorine atoms,

and

wherein any phenyl group and any 5- to 6-membered heteroaryl group areeach optionally substituted, identically or differently, with one or twogroups selected from fluorine, chlorine, methyl, ethyl, trifluoromethyl,methoxy and trifluoromethoxy,

or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or asalt thereof, or a mixture of same.

Preference is also given to compounds of the formula (I) in which:

R¹ represents a group of the formula

in which

# represents the point of attachment to the amino group,

R⁵ represents a group selected from chlorine, (C₁-C₄)-alkyl, methoxy,ethoxy, (C₃-C₅)-cycloalkyl and 4- to 6-membered heterocycle,

wherein said (C₁-C₄)-alkyl is optionally substituted with a groupselected from methoxy, —NR¹⁴R¹⁵, cyclopropyl and optionally up to threefluorine atoms,

wherein

R¹⁴ represents (C₁-C₄)-alkyl,

R¹⁵ represents (C₁-C₄)-alkyl,

or

R¹⁴ and R¹⁵ together with the nitrogen atom they are attached form a 3-to 6-membered heterocycle

wherein said (C₃-C₅)-cycloalkyl is optionally substituted with up tofour fluorine atoms,

wherein said 4- to 6-membered heterocycle is optionally substituted upto four fluorine atoms,

R⁶ represents a phenyl group,

wherein said phenyl group is optionally substituted, identically ordifferently, with one or two groups selected from fluorine, chlorine,cyano, hydroxy, —NR¹⁶R¹⁷, methyl, methoxy, ethoxy, trifluoromethoxy,methoxycarbonyl, ethoxy carbonyl and —C(═O)—NR¹⁸R¹⁹,

wherein said methyl is optionally substituted with up to three fluorineatoms,

wherein

R¹⁶ represents (C₁-C₄)-alkyl,

R¹⁷ represents (C₁-C₄)-alkyl,

or

R¹⁶ and R¹⁷ together with the nitrogen atom they are attached form a 3-to 6-membered heterocycle

wherein said 3- to 6-membered heterocycle is optionally substituted,identically or differently, with one, two or three groups selected from(C₁-C₄)-alkyl and optionally up to four fluorine atoms,

wherein

R¹⁸ represents (C₁-C₄)-alkyl,

R¹⁹ represents (C₁-C₄)-alkyl,

or

R¹⁸ and R¹⁹ together with the nitrogen atom they are attached form a 3-to 6-membered heterocycle

wherein said 3- to 6-membered heterocycle is optionally substituted,identically or differently, with one, two or three groups selected from(C₁-C₄)-alkyl and optionally up to four fluorine atoms,

R⁷ represents a hydrogen atom or (C₁-C₄)-alkyl,

wherein said (C₁-C₄)-alkyl is optionally substituted with a groupselected from (C₃-C₆)-cycloalkyl, 4- to 6-membered heterocycle, —NR²⁰R²¹and optionally with up to three fluorine atoms,

wherein said 4- to 6-membered heterocycle is optionally substituted,identically or differently, with one or two groups selected from(C₁-C₄)-alkyl and optionally up to five fluorine atoms,

and

wherein

R²⁰ represents a hydrogen atom or (C₁-C₄)-alkyl,

R²¹ represents a hydrogen atom or (C₁-C₄)-alkyl,

or

R²⁰ and R²¹ together with the nitrogen atom they are attached form a 3-to 6-membered heterocycle wherein said 3- to 6-membered heterocycle isoptionally substituted, identically or differently, with one, two orthree groups selected from (C₁-C₄)-alkyl and optionally up to fivefluorine atoms,

R⁸ represents a group selected from chlorine, (C₁-C₄)-alkyl, methoxy,ethoxy, (C₃-C₆)-cycloalkyl and 4- to 6-membered heterocycle,

wherein said (C₁-C₄)-alkyl is optionally substituted with a groupselected from methoxy —NR²²R²³, cyclopropyl and optionally up to threefluorine atoms,

wherein

R²² represents (C₁-C₄)-alkyl,

R²³ represents (C₁-C₄)-alkyl,

or

R²² and R²³ together with the nitrogen atom they are attached form a 3-to 6-membered heterocycle

wherein said (C₃-C₆)-cycloalkyl is optionally substituted with up tofour fluorine atoms,

wherein said 4- to 6-membered heterocycle is optionally substituted upto four fluorine atoms,

R⁹ represents a phenyl group,

wherein said phenyl group is optionally substituted, identically ordifferently, with one or two groups selected from fluorine, chlorine,cyano, hydroxy, —NR²⁴R²⁵, methyl, methoxy, ethoxy, trifluoromethoxy,methoxycarbonyl, ethoxy carbonyl and —C(═O)—NR²⁶R²⁷,

wherein said methyl is optionally substituted with up to three fluorineatoms,

wherein

R²⁴ represents (C₁-C₄)-alkyl,

R²⁵ represents (C₁-C₄)-alkyl,

or

R²⁴ and R²⁵ together with the nitrogen atom they are attached form a 3-to 6-membered heterocycle

wherein said 3- to 6-membered heterocycle is optionally substituted,identically or differently, with one, two or three groups selected from(C₁-C₄)-alkyl and optionally up to five fluorine atoms,

wherein

R²⁶ represents (C₁-C₄)-alkyl,

R²⁷ represents (C₁-C₄)-alkyl,

or

R²⁶ and R²⁷ together with the nitrogen atom they are attached form a 3-to 5-membered heterocycle

wherein said 3- to 5-membered heterocycle is optionally substituted,identically or differently, with one, two or three groups selected from(C₁-C₄)-alkyl and optionally up to five fluorine atoms,

R¹⁰ represents a hydrogen atom, (C₁-C₄)-alkyl or cyclopropyl,

wherein said (C₁-C₄)-alkyl is optionally substituted with a groupselected from(C₃-C₆)-cycloalkyl, 4- to 6-membered heterocycle, —NR²⁸R²⁹and optionally with up to three fluorine atoms,

wherein said (C₃-C₆)-cycloalkyl is optionally substituted with up tofour fluorine atoms,

wherein said 4- to 6-membered heterocycle is optionally substituted withup to four fluorine atoms,

and

wherein

R²⁸ represents a hydrogen atom or (C₁-C₄)-alkyl,

R²⁹ represents (C₁-C₄)-alkyl,

or

R²⁸ and R²⁹ together with the nitrogen atom they are attached form a 3-to 6-membered heterocycle

wherein said 3- to 6-membered heterocycle is optionally substituted,identically or differently, with one, two or three groups selected from(C₁-C₄)-alkyl and optionally up to five fluorine atoms,

R¹¹ represents cyclopropyl or methyl,

wherein said methyl is optionally substituted with up to three fluorineatoms,

R¹² represents a phenyl group,

wherein said phenyl group is optionally substituted, identically ordifferently, with one or two groups selected from fluorine, chlorine orcyano,

R¹³ represents a group selected from a hydrogen atom, methyl andcyclopropyl,

wherein said methyl is optionally substituted with up to three fluorineatoms, R³ represents a hydrogen atom or methyl,

wherein said methyl is optionally substituted with up to three fluorineatoms,

R³ represents a group selected from a hydrogen atom, fluorine, chlorine,cyano, (C₁-C₄)-alkyl, (C₃-C₅)-cycloalkyl, 4- to 6-membered heterocycle,5- to 6-membered heteroaryl, —C(═O)—NR³⁴R³⁵, methoxycarbonyl andethoxycarbonyl,

wherein said (C₁-C₄)-alkyl is optionally substituted with a groupselected from hydroxy, cyano, methoxy, ethoxy, methoxycarbonyl,ethoxycarbonyl and cyclopropyl and optionally up to five fluorine atoms,

wherein said (C₃-C₅)-cycloalkyl is optionally substituted with up tofour fluorine atoms,

wherein said 3- to 6-membered heterocycle is optionally substituted withup to four fluorine atoms,

wherein said 5- to 6-membered heteroaryl is optionally substituted,identically or differently, with one or two groups selected from methyl,ethyl and methoxy and optionally up to three fluorine atoms,

wherein

R³⁴ represents a hydrogen atom or (C₁-C₄)-alkyl,

R³⁵ represents (C₁-C₄)-alkyl,

or

R³⁴ and R³⁵ together with the nitrogen atom they are attached form a 3-to 6-membered heterocycle ring

wherein said 3- to 6-membered heterocycle ring is optionallysubstituted, identically or differently, with one or two groups selectedfrom a fluorine atom, methyl, difluoromethyl, trifluoromethyl andtrifluoromethoxy,

or

R² and R³ together with the carbon atoms they are attached form a phenylor a 4- to 6-membered carbocycle,

wherein said phenyl group is optionally substituted, identically ordifferently, with one or two groups selected from fluorine, chlorine,methyl, trifluoromethyl, methxoy and trifluoromethoxy,

wherein said 4- to 6-membered carbocycle is optionally substituted,identically or differently, with one or two groups selected from oxo,methyl, ethyl, trifluoromethyl and (C₁-C₄)-alkoxycarbonyl and optionallyup to four fluorine atoms,

R⁴ represents a group selected from a hydrogen atom, (C₁-C₄)-alkyl,hydroxy and cyclopropyl,

wherein said (C₁-C₄)-alkyl is optionally substituted with a groupselected from hydroxy, methoxy and cyclopropyl and optionally up to fivefluorine atoms,

or

R³ and R⁴ together with the carbon atoms they are attached form a a 4-to 6-membered carbocycle, a 4- to 6-membered heterocycle, a 5- to6-membered heteroaryl group or a phenyl ring,

wherein said 4- to 6-membered heterocycle is optionally substituted,identically or differently, with one or two groups selected from oxo,methyl, ethyl, trifluoromethyl and (C₁-C₄)-alkoxycarbonyl and optionallyup to four fluorine atoms,

wherein said 4- to 6-membered carbocycle is optionally substituted,identically or differently, with one or two groups selected from oxo,hydroxyl, methyl, ethyl, trifluoromethyl and (C₁-C₄)-alkoxycarbonyl andoptionally up to four fluorine atoms,

and

wherein any phenyl group and any 5- to 6-membered heteroaryl group areeach optionally substituted, identically or differently, with one or twogroups selected from fluorine, chlorine, methyl, ethyl, trifluoromethyl,methxoy and trifluoromethoxy,

or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or asalt thereof, or a mixture of same.

Preference is also given to compounds of the formula (I) in which,

R¹ represents a group of the formula

in which

# represents the point of attachment to the amino group,

R⁵ represents a group selected from chlorine, methyl, ethyl, methoxy andcyclopropyl

wherein said methyl is optionally substituted with a group selected frommethoxy and cyclopropyl and optionally up to three fluorine atoms,

R⁶ represents a phenyl group,

wherein said phenyl group is optionally substituted, identically ordifferently, with one or two groups selected from fluorine, chlorine,cyano, methyl, methoxy, ethoxy, trifluoromethoxy, methoxycarbonyl andethoxycarbonyl,

wherein said methyl is optionally substituted with up to three fluorineatoms,

R⁷ represents a hydrogen atom, methyl, ethyl or cyclopropyl,

wherein said methyl and ethyl are optionally substituted withcyclopropyl and optionally with up to three fluorine atoms,

R⁸ represents a group selected from chlorine, methyl, ethyl, methoxy andcyclopropyl,

wherein said methyl is optionally substituted with a group selected frommethoxy and cyclopropyl and optionally up to three fluorine atoms,

R⁹ represents a phenyl group,

wherein said phenyl group is optionally substituted, identically ordifferently, with one or two groups selected from fluorine, chlorine,cyano, methyl, methoxy, ethoxy, trifluoromethoxy, methoxycarbonyl andethoxy carbonyl,

wherein said methyl is optionally substituted with up to three fluorineatoms,

R¹⁰ represents a hydrogen atom, methyl, ethyl or cyclopropyl,

wherein said methyl and ethyl are optionally substituted withcyclopropyl and optionally with up to three fluorine atoms,

R¹¹ represents cyclopropyl or methyl,

wherein said methyl is optionally substituted with up to three fluorineatoms,

R¹² represents a phenyl group,

wherein said phenyl group is optionally substituted, identically ordifferently, with one or two groups selected from fluorine, chlorine orcyano,

R¹³ represents a group selected from a hydrogen atom, methyl andcyclopropyl,

wherein said methyl is optionally substituted with up to three fluorineatoms,

R² represents a hydrogen atom or methyl,

R³ represents a group selected from a hydrogen atom, fluorine, chlorine,cyano, (C₁-C₄)-alkyl, cyclopropyl, 4- to 6-membered heterocycle, 5- to6-membered heteroaryl, —C(═O)—NR³⁴R³⁵, methoxycarbonyl andethoxycarbonyl,

wherein said (C₁-C₄)-alkyl is optionally substituted with a groupselected from hydroxy, ethoxycarbonyl and cyclopropyl and optionally upto three fluorine atoms,

wherein said 5- to 6-membered heteroaryl is optionally substituted,identically or differently, with one or two groups selected from methyl,ethyl and methoxy and optionally up to two fluorine atoms,

wherein

R³⁴ represents a hydrogen atom, methyl or ethyl,

R³⁵ represents methyl or ethyl,

or

R³⁴ and R³⁵ together with the nitrogen atom they are attached form a 4-to 6-membered heterocycle ring

wherein said 4- to 6-membered heterocycle ring is optionallysubstituted, identically or differently, with one or two groups selectedfrom a fluorine atom, methyl, difluoromethyl and trifluoromethyl,

or

R² and R³ together with the carbon atoms they are attached form a phenylor a 5- to 6-membered carbocycle, wherein said phenyl group isoptionally substituted with one or two fluorine atoms,

wherein said 5- to 6-membered carbocycle is optionally substituted, withup to four fluorine atoms,

R⁴ represents a group selected from a hydrogen atom, methyl andcyclopropyl,

wherein said methyl is optionally substituted with up to three fluorineatoms,

or

R³ and R⁴ together with the carbon atoms they are attached form a 5- to6-membered carbocycle, a 4- to 6-membered heterocycle, a 5- to6-membered heteroaryl group or a phenyl ring,

wherein said 4- to 6-membered heterocycle is optionally substituted,identically or differently, with (C₁-C₄)-alkoxycarbonyl and optionallyup to four fluorine atoms,

wherein said 4- to 6-membered carbocycle is optionally substituted withup to four fluorine atoms, and

wherein any phenyl group and any 5- to 6-membered heteroaryl group areeach optionally substituted with one or two fluorine aoms,

or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or asalt thereof, or a mixture of same.

Preference is also given to compounds of the formula (I) in which

R¹ represents a group of the formula

-   -   in which    -   # represents the point of attachment to the amino group,    -   R⁵ represents a group selected from chlorine, methyl, ethyl,        methoxy or cyclopropyl,        -   wherein said methyl and ethyl are optionally substituted            with methoxy or optionally with up to three fluorine atoms,        -   wherein said methoxy is optionally substituted with up to            three fluorine atoms,    -   R⁶ represents 5-fluoropyridin-2-yl,        6-trifluoromethylpyridin-3-yl or cyclohexyl,        -   or        -   represents a group of the formula

-   -   -   in which        -   ## represents the point of attachment to the pyrazole ring,        -   R³⁸ represents a hydrogen atom or fluorine,        -   R^(38a) represents a hydrogen atom,        -   R³⁹ represents a hydrogen atom,        -   R^(39a) represents a hydrogen atom or cyano,        -   R⁴⁰ represents a hydrogen atom, fluorine, chlorine, cyano,            methyl, difluoromethyl, trifluoromethyl, methoxy, ethoxy,            difluoromethoxy, trifluoromethoxy, methoxycarbonyl or            ethoxycarbonyl,        -   R⁷ represents a hydrogen atom, methyl, ethyl,            cyclopropylmethyl, 2-cyclopropylethyl or 2,2-difluoroethyl,        -   with the proviso that if R⁵ is methoxy, difluoromethoxy or            trifluoromethoxy then R⁷ is different from hydrogen,        -   with the proviso that if R⁶ is 2-pyridinyl then R⁷ is            different from hydrogen,

and stereoisomers, tautomers, hydrates, solvates, and salts thereof, andmixtures of same.

Preference is also given to compounds of the formula (I) in which

R¹ represents a group of the formula

-   -   in which    -   # represents the point of attachment to the amino group,    -   R⁵ represents a group selected from chlorine, methyl, ethyl,        methoxy or cyclopropyl,        -   wherein said methyl and ethyl are optionally substituted            with methoxy or optionally with up to three fluorine atoms,        -   wherein said methoxy is optionally substituted with up to            three fluorine atoms,    -   R⁶ represents 5-fluoropyridin-2-yl,        6-trifluoromethylpyridin-3-yl or cyclohexyl,        -   or        -   represents a group of the formula

-   -   -   in which        -   ## represents the point of attachment to the pyrazole ring,        -   R³⁸ represents a hydrogen atom,        -   R^(38a) represents a hydrogen atom,        -   R³⁹ represents a hydrogen atom,        -   R^(39a) represents a hydrogen atom,        -   R⁴⁰ represents a hydrogen atom, fluorine, chlorine, cyano,            methyl, difluoromethyl, trifluoromethyl, methoxy, ethoxy,            difluoromethoxy, trifluoromethoxy, methoxycarbonyl or            ethoxycarbonyl,

    -   R⁷ represents a hydrogen atom, methyl, ethyl, cyclopropylmethyl,        2-cyclopropylethyl or 2,2-difluoroethyl,

    -   with the proviso that if R⁵ is methoxy, difluoromethoxy or        trifluoromethoxy then R⁷ is different from hydrogen,

    -   with the proviso that if R⁶ represents 5-fluoropyridin-2-yl or        6-trifluoromethylpyridin-3-yl then R⁷ is different from        hydrogen,

and stereoisomers, tautomers, hydrates, solvates, and salts thereof, andmixtures of same.

Preference is also given to compounds of the formula (I) in which

-   -   R⁵ represents methyl, ethyl or methoxy

and stereoisomers, tautomers, hydrates, solvates, and salts thereof, andmixtures of same.

Preference is also given to compounds of the formula (I) in which

R¹ represents group of the formula,

-   -   R⁸ represents a group selected from chlorine, methyl, ethyl,        methoxy and cylcopropyl,    -   R⁹ represents pyridyl or        4-cyanopentacyclo[4.2.0.0^(2,5).0^(3,8).0^(4,7)]octan-1-yl,        -   or        -   represents a group of the formula

-   -   -   in which        -   ## represents the point of attachment to the pyrazole ring,        -   R^(38b) represents a hydrogen atom or fluorine,        -   R^(38c) represents a hydrogen atom,        -   R^(39b) represents a hydrogen atom,        -   R^(39c) represents a hydrogen atom,        -   R^(40a) represents a hydrogen atom, fluorine, chlorine,            cyano, methyl, difluoromethyl, trifluoromethyl, methylamino,            methoxy, difluoromethoxy, trifluoromethoxy or cyclopropyl,        -   wherein said pyridyl is optionally substituted with            fluorine, methyl, difluoromethyl, trifluoromethyl or            methoxy,

    -   R¹⁰ represents a hydrogen atom, methyl, ethyl,        2,2-difluoroethyl, cyclopropylmethyl, cyclobutylmethyl,        2-cyclopropylethyl, 2-cyclopropyl-2-hydroxypropyl,        2-cyclopropyl-2-hydroxyethyl, 2-methoxyethyl, or cyclopropyl,        -   wherein said methyl and ethyl are optionally substituted            with a group selected from cyclopropyl, methoxy or            optionally up to three fluorine atoms and is optionally            additionally substituted with hydroxy,

    -   with the proviso that if R⁹ is pyridyl then R¹⁰ is different        from hydrogen,

    -   with the proviso that if R⁸ is methoxy then R¹⁰ is different        from hydrogen,

and stereoisomers, tautomers, hydrates, solvates, and salts thereof, andmixtures of same.

Preference is also given to compounds of the formula (I) in which

R¹ represents group of the formula,

-   -   R⁸ represents a group selected from chlorine, methyl, ethyl,        methoxy and cylcopropyl,    -   R⁹ represents pyridyl or        4-cyanopentacyclo[4.2.0.0^(2,5).0^(3,8).0^(4,7)]octan-1-yl,        -   or        -   represents a group of the formula

-   -   -   in which        -   ## represents the point of attachment to the pyrazole ring,        -   R^(38b) represents a hydrogen atom,        -   R^(38c) represents a hydrogen atom,        -   R^(39b) represents a hydrogen atom,        -   R^(39c) represents a hydrogen atom,        -   R^(40a) represents a hydrogen atom, fluorine, chlorine,            cyano, methyl, difluoromethyl, trifluoromethyl, methylamino,            methoxy, difluoromethoxy, trifluoromethoxy or cyclopropyl,        -   wherein said pyridyl is optionally substituted with            fluorine, methyl, difluoromethyl, trifluoromethyl or            methoxy,

    -   R¹⁰ represents a hydrogen atom, methyl, ethyl,        2,2-difluoroethyl, cyclopropylmethyl, cyclobutylmethyl,        2-cyclopropylethyl, 2-cyclopropyl-2-hydroxypropyl,        2-cyclopropyl-2-hydroxyethyl, 2-methoxyethyl, or cyclopropyl,        -   wherein said methyl and ethyl are optionally substituted            with a group selected from cyclopropyl, methoxy or            optionally up to three fluorine atoms and is optionally            additionally substituted with hydroxy,

    -   with the proviso that if R⁹ is pyridyl then R¹⁰ is different        from hydrogen,

    -   with the proviso that if R⁸ is methoxy then R¹⁰ is different        from hydrogen,

and stereoisomers, tautomers, hydrates, solvates, and salts thereof, andmixtures of same.

Preference is also given to compounds of the formula (I) in which

R¹ represents group of the formula,

-   -   R⁸ represents a group selected from methyl, ethyl or methoxy,

and stereoisomers, tautomers, hydrates, solvates, and salts thereof, andmixtures of same.

Preference is also given to compounds of the formula (I) in which

-   -   R⁹ represents pyridyl    -   wherein said pyridyl is optionally substituted with fluorine,        methyl, difluoromethyl, trifluoromethyl or methoxy,

and stereoisomers, tautomers, hydrates, solvates, and salts thereof, andmixtures of same.

Preference is also given to compounds of the formula (I) in which

-   -   R⁹ represents        4-cyanopentacyclo[4.2.0.0^(2,5).0^(3,8).0^(4,7)]octan-1-yl,

and stereoisomers, tautomers, hydrates, solvates, and salts thereof, andmixtures of same.

Preference is also given to compounds of the formula (I) in which

R¹ represents group of the formula,

-   -   R¹¹ represents methyl,    -   R¹² represents a group of the formula

-   -   -   in which        -   ## represents the point of attachment to the pyrazole ring,        -   R^(38d) represents a hydrogen atom,        -   R^(38e) represents a hydrogen atom,        -   R^(39d) represents a hydrogen atom,        -   R^(39e) represents a hydrogen atom,        -   R^(40b) represents fluorine or cyano,

    -   R¹³ represents a group selected from a hydrogen atom or methyl,

and stereoisomers, tautomers, hydrates, solvates, and salts thereof, andmixtures of same.

Preference is also given to compounds of the formula (I) in which

R² represents a hydrogen atom, methyl or difluoromethyl,

and stereoisomers, tautomers, hydrates, solvates, and salts thereof, andmixtures of same.

Preference is also given to compounds of the formula (I) in which

-   R³ represents a group selected from a hydrogen atom, fluorine,    chlorine, bromine, cyano, hydroxy, nitro, amino, ethylamino,    dimethylamino, —O—C(═O)—NR³⁶R³⁷, —O—C(═O)—OR^(37a),    —NH—C(═O)—OR^(37a), (C₁-C₄)-alkyl, methoxy, cyclopropyl, cyclobutyl,    4-membered heterocycle, 1,3,4-oxadiazol-2-yl,    2-(trifluoromethyl)-1,3-dioxolan-2-yl, —(CH₂)_(q)—C(═O)—NR³⁴R³⁵,    methoxycarbonyl and ethoxycarbonyl,    -   wherein said (C₁-C₄)-alkyl is optionally substituted,        identically or differently, with one or two groups selected from        hydroxy, methoxy, methoxycarbonyl, ethoxycarbonyl,        dimethylamino, a 4-membered azaheterocycle and cyclopropyl and        optionally up to three fluorine atoms,        -   wherein said 4-membered azaheterocycle is optionally            substituted with up to two fluorine atoms,    -   wherein said methoxy is optionally substituted with cyano,        cyclopropyl and optionally up to three fluorine atoms,    -   wherein said cyclopropyl and cyclobutyl are optionally        substituted with hydroxy,    -   wherein said 4-membered heterocycle is optionally substituted        with hydroxy,    -   wherein said 1,3,4-oxadiazol-2-yl is optionally substituted with        methyl,    -   wherein    -   q is 0,    -   R³⁴ represents methyl,    -   R³⁵ represents methyl,    -   or    -   R³⁴ and R³⁵ together with the nitrogen atom they are attached        form a 4- to 6-membered heterocycle ring        -   wherein said 4- to 6-membered heterocycle ring is optionally            substituted, identically or differently, with one or two            groups selected from a fluorine atom, methyl, difluoromethyl            and trifluoromethyl,    -   wherein    -   R³⁶ represents a methyl atom,    -   R³⁷ represents a hydrogen atom or methyl,    -   R^(37a) represents methyl,

and stereoisomers, tautomers, hydrates, solvates, and salts thereof, andmixtures of same.

Preference is also given to compounds of the formula (I) in which

R² and R³ together with the carbon atoms they are attached form a 5- to6-membered carbocycle, a pyrrolidinyl, a pyridyl or a phenyl ring,

wherein said 5- to 6-membered carbocycle is optionally substituted,identically or differently, with one or two groups selected from oxo,methyl, trifluoromethyl and hydroxy,

wherein said pyrrolidinyl is substituted with propyl ortert.-butoxycarbonyl,

and stereoisomers, tautomers, hydrates, solvates, and salts thereof, andmixtures of same.

Preference is also given to compounds of the formula (I) in which

-   R⁴ represents a group selected from a hydrogen atom, methyl,    2-hydroxypropan-2-yl, fluoromethyl, difluoromethyl, methoxycarbonyl,    ethoxycarbonyl and hydroxy,

and stereoisomers, tautomers, hydrates, solvates, and salts thereof, andmixtures of same.

Preference is also given to compounds of the formula (I) in which

R³ and R⁴ together with the carbon atoms they are attached form a 5- to6-membered carbocycle, a pyrrolidinyl ring or a piperidinyl ring, apyridyl group or a phenyl ring,

-   -   wherein said pyrrolidinyl ring is substituted with propyl or        tert-butoxycarbonyl,    -   wherein said piperidinyl ring is substituted with propyl or        tert-butoxycarbonyl,    -   wherein said 5- to 6-membered carbocycle is optionally        substituted, identically or differently, with one or two groups        selected from oxo, hydroxy and methyl,

and stereoisomers, tautomers, hydrates, solvates, and salts thereof, andmixtures of same.

Preference is also given to compounds of the formula (I) in which

R¹ represents group of the formula,

in which

# represents the point of attachment to the amino group,

R⁵ represents a group selected from chlorine, methyl, ethyl, methoxy andcyclopropyl

wherein said methyl is optionally substituted with a group selected frommethoxy and cyclopropyl and optionally up to three fluorine atoms,

R⁶ represents a phenyl group,

wherein said phenyl group is optionally substituted, identically ordifferently, with one or two groups selected from fluorine, chlorine,cyano, methyl, methoxy, ethoxy, trifluoromethoxy, methoxycarbonyl andethoxy carbonyl,

wherein said methyl is optionally substituted with up to three fluorineatoms,

R⁷ represents a hydrogen atom, methyl, ethyl or cyclopropyl,

wherein said methyl and ethyl are optionally substituted withcyclopropyl and optionally with up to three fluorine atoms,

and stereoisomers, tautomers, hydrates, solvates, and salts thereof, andmixtures of same.

Preference is also given to compounds of the formula (I) in which

R¹ represents group of the formula,

in which

# represents the point of attachment to the amino group,

R⁸ represents a group selected from chlorine, methyl, ethyl, methoxy andcyclopropyl,

wherein said methyl is optionally substituted with a group selected frommethoxy and cyclopropyl and optionally up to three fluorine atoms,

R⁹ represents a phenyl group,

wherein said phenyl group is optionally substituted, identically ordifferently, with one or two groups selected from fluorine, chlorine,cyano, methyl, methoxy, ethoxy, trifluoromethoxy, methoxycarbonyl andethoxy carbonyl,

wherein said methyl is optionally substituted with up to three fluorineatoms,

R¹⁰ represents a hydrogen atom, methyl, ethyl or cyclopropyl,

wherein said methyl and ethyl are optionally substituted withcyclopropyl and optionally with up to three fluorine atoms,

and stereoisomers, tautomers, hydrates, solvates, and salts thereof, andmixtures of same.

Preference is also given to compounds of the formula (I) in which

R¹ represents group of the formula,

in which

# represents the point of attachment to the amino group,

R¹¹ represents cyclopropyl or methyl,

wherein said methyl is optionally substituted with up to three fluorineatoms,

R¹² represents a phenyl group,

wherein said phenyl group is optionally substituted, identically ordifferently, with one or two groups selected from fluorine, chlorine orcyano,

R¹³ represents a group selected from a hydrogen atom, methyl andcyclopropyl,

wherein said methyl is optionally substituted with up to three fluorineatoms,

and stereoisomers, tautomers, hydrates, solvates, and salts thereof, andmixtures of same.

Preference is also given to compounds of the formula (I) in which

R² represents methyl,

and stereoisomers, tautomers, hydrates, solvates, and salts thereof, andmixtures of same.

Preference is also given to compounds of the formula (I) in which

R² represents a hydrogen atom,

and stereoisomers, tautomers, hydrates, solvates, and salts thereof, andmixtures of same.

Preference is also given to compounds of the formula (I) in which

R³ represents a group selected from a hydrogen atom, fluorine, chlorine,cyano, (C₁-C₄)-alkyl, cyclopropyl, 4- to 6-membered heterocycle, 5- to6-membered heteroaryl, —C(═O)—NR³⁴R³⁵, methoxycarbonyl andethoxycarbonyl,

wherein said (C₁-C₄)-alkyl is optionally substituted with a groupselected from hydroxy, ethoxycarbonyl and cyclopropyl and optionally upto three fluorine atoms,

wherein said 5- to 6-membered heteroaryl is optionally substituted,identically or differently, with one or two groups selected from methyl,ethyl and methoxy and optionally up to two fluorine atoms,

wherein

R³⁴ represents a hydrogen atom, methyl or ethyl,

R³⁵ represents methyl or ethyl,

or

R³⁴ and R³⁵ together with the nitrogen atom they are attached form a 4-to 6-membered heterocycle ring

wherein said 4- to 6-membered heterocycle ring is optionallysubstituted, identically or differently, with one or two groups selectedfrom a fluorine atom, methyl, difluoromethyl and trifluoromethyl,

and stereoisomers, tautomers, hydrates, solvates, and salts thereof, andmixtures of same.

Preference is also given to compounds of the formula (I) in which

R³ represents a group selected from a hydrogen atom, chlorine, cyano,(C₁-C₄)-alkyl, —C(═O)—NR³⁴R³⁵ and ethoxycarbonyl,

wherein said (C₁-C₄)-alkyl is optionally substituted with a groupselected from hydroxyl and ethoxycarbonyl and optionally up to threefluorine atoms,

wherein

R³⁴ represents methyl or ethyl,

R³⁵ represents methyl or ethyl,

or

R³⁴ and R³⁵ together with the nitrogen atom they are attached form a 4-to 6-membered heterocycle ring

wherein said 4- to 6-membered heterocycle ring is optionallysubstituted, identically or differently, with one or two groups selectedfrom a fluorine atom, methyl, difluoromethyl and trifluoromethyl,

and stereoisomers, tautomers, hydrates, solvates, and salts thereof, andmixtures of same.

Preference is also given to compounds of the formula (I) in which

R³ represents a hydrogen atom,

and stereoisomers, tautomers, hydrates, solvates, and salts thereof, andmixtures of same.

Preference is also given to compounds of the formula (I) in which

R³ represents chlorine,

and stereoisomers, tautomers, hydrates, solvates, and salts thereof, andmixtures of same.

Preference is also given to compounds of the formula (I) in which

R² and R³ together with the carbon atoms they are attached form a phenylor a 5- to 6-membered carbocycle,

wherein said phenyl group is optionally substituted with one or twofluorine atoms,

wherein said 5- to 6-membered carbocycle is optionally substituted, withup to four fluorine atoms,

and stereoisomers, tautomers, hydrates, solvates, and salts thereof, andmixtures of same.

Preference is also given to compounds of the formula (I) in which

R² and R³ together with the carbon atoms they are attached form a phenylor a 5- to 6-membered carbocycle, and stereoisomers, tautomers,hydrates, solvates, and salts thereof, and mixtures of same.

Preference is also given to compounds of the formula (I) in which

R⁴ represents a group selected from a hydrogen atom, methyl andcyclopropyl,

wherein said methyl is optionally substituted with up to three fluorineatoms,

and stereoisomers, tautomers, hydrates, solvates, and salts thereof, andmixtures of same.

Preference is also given to compounds of the formula (I) in which

R⁴ represents methyl,

wherein said methyl is optionally substituted with up to three fluorineatoms,

and stereoisomers, tautomers, hydrates, solvates, and salts thereof, andmixtures of same.

Preference is also given to compounds of the formula (I) in which

R⁴ represents methyl,

and stereoisomers, tautomers, hydrates, solvates, and salts thereof, andmixtures of same.

Preference is also given to compounds of the formula (I) in which

R³ and R⁴ together with the carbon atoms they are attached form a 5- to6-membered carbocycle, a 4- to 6-membered heterocycle, a 5- to6-membered heteroaryl group or a phenyl ring,

wherein said 4- to 6-membered heterocycle is optionally substituted,identically or differently, with (C₁-C₄)-alkoxycarbonyl and optionallyup to four fluorine atoms,

wherein said 4- to 6-membered carbocycle is optionally substituted withup to four fluorine atoms,

and

wherein any phenyl group and any 5- to 6-membered heteroaryl group areeach optionally substituted with one or two fluorine aoms,

and stereoisomers, tautomers, hydrates, solvates, and salts thereof, andmixtures of same.

Preference is also given to compounds of the formula (I) in which

R³ and R⁴ together with the carbon atoms they are attached form a 5- to6-membered carbocycle, a 4- to 6-membered heterocycle or a phenyl ring,

wherein said 4- to 6-membered heterocycle is optionally substituted,identically or differently, with (C₁-C₄)-alkoxycarbonyl and optionallyup to four fluorine atoms,

wherein said 4- to 6-membered carbocycle is optionally substituted withup to four fluorine atoms,

and

wherein any phenyl group and any 5- to 6-membered heteroaryl group areeach optionally substituted with one or two fluorine aoms,

and stereoisomers, tautomers, hydrates, solvates, and salts thereof, andmixtures of same.

Preference is also given to compounds of the formula (I) in which

R³ and R⁴ together with the carbon atoms they are attached form a 5- to6-membered carbocycle, a 4- to 6-membered heterocycle or a phenyl ring,

wherein said 4- to 6-membered heterocycle is optionally substituted with(C₁-C₄)-alkoxycarbonyl,

and stereoisomers, tautomers, hydrates, solvates, and salts thereof, andmixtures of same.

In a particular further embodiment of the first aspect, the presentinvention covers combinations of two or more of the above mentionedembodiments under the heading “further embodiments of the first aspectof the present invention”.

The present invention covers any sub-combination within any embodimentor aspect of the present invention of compounds of general formula (I),supra.

The present invention covers the compounds of general formula (I) whichare disclosed in the Example Section of this text, infra.

In accordance with a second aspect, the present invention covers methodsof preparing compounds of general formula (I) as defined supra, saidmethods comprising the step

[A] of allowing an intermediate compound of general formula (II-A),(II-B) or (II-C):

in which R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹, R¹² and R¹³ are as defined forthe compound of general formula (I) as defined supra,

to react in the presence of sodium iodide and a suitable base, with4,6-dichloropyrimidine (III),

or

to react in the presence of a suitable Broenstedt acid or Lewis acidwith 4,6-dichloropyrimidine (III),

or

to react in the presence of a suitable base with 4,6-dichloropyrimidine(III),

or

to react in the presence of a suitable base and in the presence of asuitable catalyst, in particular a suitable palladium catalyst, and asuitable ligand with 4,6-dichloropyrimidine (III),

thereby giving a compound of general formula (IV-A), (IV-B) and (IV-C),respectively:

in which R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹, R¹² and R¹³ are as defined forthe compound of general formula (I) as defined supra,

which is allowed to react in the presence of a suitable base and whereappropiate in the presence of a suitable catalyst, in particular asuitable palladium catalyst, with a pyrazole of general formula (V),

in which R², R³ and R⁴ are as defined for the compound of generalformula (I) as defined supra,

thereby giving a compound of general formula (I-A), (I-B) and (I-C),respectively.

in which R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹, R¹² and R¹³ are asdefined for the compound of general formula (I) as defined supra,

then optionally converting said compound into solvates, salts and/orsolvates of such salts using the corresponding (i) solvents and/or (ii)bases or acids.

or

[B] of allowing an intermediate compound of general formula (IV-A),(IV-B) or (IV-C):

in which R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹, R¹² and R¹³ are as defined forthe compound of general formula (I) as defined supra,

to react in the presence of a hydrazine equivalent, in particularhydrazine monohydrate,

thereby giving a compound of general formula (V-A), (V-B) and (V-C),respectively,

which is allowed to react in the presence of a 1,3 dicarbonyl compoundof general formula (VI),

in which R², R³ and R⁴ are as defined for the compound of generalformula (I) as defined supra,

thereby giving a compound of general formula (I-A), (I-B) and (I-C),respectively,

in which R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹, R¹² and R¹³ are asdefined for the compound of general formula (I) as defined supra,

then optionally converting said compound into solvates, salts and/orsolvates of such salts using the corresponding (i) solvents and/or (ii)bases or acids.

or

[C] of allowing an intermediate compound of general formula (IV-A),(IV-B) or (IV-C):

in which R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹, R¹² and R¹³ are as defined forthe compound of general formula (I) as defined supra,

to react in the presence of a hydrazine equivalent, in particularhydrazine monohydrate,

thereby giving a compound of general formula (V-A), (V-B) and (V-C),respectively,

which is allowed to react in the presence of a 1,3 dicarbonyl compoundof general formula (VII),

in which R² and R³ are as defined for the compound of general formula(I) as defined supra, and

T¹ represents methoxy or ethoxy,

thereby giving a compound of general formula (I-D), (I-E) and (I-F),respectively,

in which R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹, R¹² and R¹³ are asdefined for the compound of general formula (I) as defined supra,

then optionally converting said compound into solvates, salts and/orsolvates of such salts using the corresponding (i) solvents and/or (ii)bases or acids.

or

[D] of allowing an intermediate compound of general formula (VIII) :

in which R², R³ and R⁴ are as defined for the compound of generalformula (I) as defined supra,

to react in the presence of a suitable base with 4,6-dichloropyrimidine(III),

thereby giving a compound of general formula (IX),

in which R¹, R², R³ and R⁴ are as defined for the compound of generalformula (I) as defined supra,

which is allowed to react

b) in the presence of a suitable Broenstedt acid or Lewis acid with anintermediate compound of general formula (II-A), (II-B) or (II-C),

or

c) in the presence of a suitable base with an intermediate compound ofgeneral formula (II-A), (II-B) or (II-C),

or

d) in the presence of a suitable base and in the presence of a suitablecatalyst, in particular a suitable palladium catalyst, and a suitableligand with an intermediate compound of general formula (II-A), (II-B)or (II-C),

in which R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹, R¹² and R¹³ are as defined forthe compound of general formula (I) as defined supra, and

thereby giving a compound of general formula (I-A), (I-B) and (I-C),respectively,

in which R², R³, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹, R¹² and R¹³ are asdefined for the compound of general formula (I) as defined supra,

then optionally converting said compound into solvates, salts and/orsolvates of such salts using the corresponding (i) solvents and/or (ii)bases or acids.

or

[E] of allowing 4,6-dichloropyrimidine (III),

to react with a hydrazine equivalent, in particular hydrazinemonohydrate,

thereby giving a compound of general formula (X),

which is allowed to react in the presence of a 1,3 dicarbonyl compoundof general formula (VI),

in which R², R³ and R⁴ are as defined for the compound of generalformula (I) as defined supra,

thereby giving a compound of general formula (VII),

in which R¹, R², R³ and R⁴ are as defined for the compound of generalformula (I) as defined supra,

which is allowed to react

b) in the presence of a suitable Broenstedt acid with an intermediatecompound of general formula (II-A), (II-B) or (II-C),

or

c) in the presence of a suitable base with an intermediate compound ofgeneral formula (II-A), (II-B) or (II-C),

or

d) in the presence of a suitable base and in the presence of a suitablecatalyst, in particular a suitable palladium catalyst, and a suitableligand with an intermediate compound of general formula (II-A), (II-B)or (II-C),

in which R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹, R¹² and R¹³ are as defined forthe compound of general formula (I) as defined supra, and

thereby giving a compound of general formula (I-A), (I-B) and (I-C),respectively,

in which R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹, R¹² and R¹³ are asdefined for the compound of general formula (I) as defined supra,

then optionally converting said compound into solvates, salts and/orsolvates of such salts using the corresponding (i) solvents and/or (ii)bases or acids.

or

[F] of allowing compound of general formula (IX),

in which R², R³ and R⁴ are as defined for the compound of generalformula (I) as defined supra,

which is allowed to react

b) in the presence of a suitable Broenstedt acid or a suitable base withan intermediate compound of general formula (X),

or

c) in the presence of a suitable base with an intermediate compound ofgeneral formula (X)

or

d) in the presence of a suitable base and in the presence of a suitablecatalyst, in particular a suitable palladium catalyst, and a suitableligand with an intermediate compound of general formula (X),

in which R⁵, and R⁷ are as defined for the compound of general formula(I) as defined supra, and

thereby giving a compound of general formula (XI),

in which R², R³, R⁴, R⁵ and R⁷ are as defined for the compound ofgeneral formula (I) as defined supra,

which is allowed to react in the presence of a suitable base and in thepresence of a suitable palladium catalyst with a compound of generalformula (XII),

in which R⁶ is as defined for the compound of general formula (I) asdefined supra, and

X is chlorine, bromine, iodine or triflate,

thereby giving a compound of general formula (I-A),

in which R², R³, R⁴, R⁵, R⁶ and R⁷ are as defined for the compound ofgeneral formula (I) as defined supra,

then optionally converting said compound into solvates, salts and/orsolvates of such salts using the corresponding (i) solvents and/or (ii)bases or acids.

The compounds of the formulae (I-A), (I-B), (I-C), (I-D), (I-E) and(I-F) form a subset of the compounds of the formula (I) according to theinvention.

The compounds of the formulae (II-A), (II-B), (II-C), (III), (V), (VI),(VII) and (VIII) are commercially available, known from the literatureor can be prepared analogously to processes known from the literature.

The preparation processes described can be illustrated in an exemplarymanner by the synthesis schemes below (Schemes 1 to 3):

[a): NaI, DIPEA, DMF, 80° C.; b): DBU, NMP, 190° C.].

[a): Cs₂CO₃, DMF, r.t.; b): Pd₂(dba)₃, Xantphos, NaOPh, dioxane, 80°C.].

a): Pd₂(dba)₃, Xantphos, NaOPh, dioxane, 80° C.; b): PdCl(C₃H₅)dppb,KOAc, DMAc, 150° C.

Further preparation processes used for preparing compounds of thepresent invention can be illustrated in an exemplary manner by thesynthesis schemes below (Schemes 8 to 13):

a): THF, 0° C. to rt; b): MgSO₄, n-Butylacetate AcOH, 0° C. to 110° C.;c): diethyl [bromo(difluoro)methyl]phosphonate, KOH, MeCN/H₂O, −20° C.;d): NaOH, THF, MeOH, H₂O, rt; e): diphenylphosporyl azide, NEt₃, t-BuOH,Toluene, rt to 80° C.; f): TFA, CH₂Cl₂, rt. 3

a): aq. Methylamine solution, SiO₂; b): difluoroacetic anhydride, NEt₃,MTBE, 0° C. to rt; c): hydrazine monohydrate, MeOH, −20° C. to rt; d):4,6-dichloropyrimidine, Cs₂CO₃, DMF

a): Nickel (II) chloride dimethoxyethane adduct,4,4′-di-tert-butyl-2,2′-bipyridine, Ir(F₂(CF3)ppy]₂(dtbbpy)PF₆,tris(trimethyl)silane, LiOH, dimethoxyethane, two 34 W blue LEDs.

a): NaOAc, DMSO, rt; b) L: hydrazine monohydrate, EtOH, rt; c):(6-chloropyrimidin-4-yl)hydrazine, EtOH, reflux; d): K₂CO₃, MeOH, 0° C.;e): Cs₂CO₃, MeI, DMF, rt.

a): Cs₂CO₃, DMF, rt; b): Pd(dba)₂, XantPhos, NaOPh, 85° C.; c): TMSCF₃,TBAFH₂O, THF/toluene, −20° C. to rt.

The present invention covers methods of preparing compounds of thepresent invention of general formula (I), said methods comprising thesteps as described in the Experimental Section herein.

The schemes and procedures described below illustrate synthetic routesto the compounds of general formula (I) of the invention and are notintended to be limiting. It is clear to the person skilled in the artthat the order of transformations as exemplified in schemes 1, 2, 3 and4 can be modified in various ways. The order of transformationsexemplified in these schemes is therefore not intended to be limiting.In addition, interconversion of any of the substituents, R¹, R², R³, R⁴,R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹, R¹², R¹³, R¹⁴, R¹⁵, R¹⁶, R¹⁷, R^(A), T¹,Q, and X can be achieved before and/or after the exemplifiedtransformations. These modifications can be such as the introduction ofprotecting groups, cleavage of protecting groups, reduction or oxidationof functional groups, halogenation, metallation, substitution or otherreactions known to the person skilled in the art. These transformationsinclude those which introduce a functionality which allows for furtherinterconversion of substituents. Appropriate protecting groups and theirintroduction and cleavage are well-known to the person skilled in theart (see for example T. W. Greene and P. G. M. Wuts in Protective Groupsin Organic Synthesis, 3^(rd) edition, Wiley 1999). Specific examples aredescribed in the subsequent paragraphs.

Suitable bases for the process step (II-A), (II-B) or(II-C)+(III)→(IV-A), (IV-B) or (IV-C) and (II-A), (II-B) or(II-C)+(IX)→(I-A), (I-B) or (I-C), when using approach a) or c) are thecustomary inorganic or organic bases. These preferably include alkalimetal hydroxides, for example lithium hydroxide, sodium hydroxide orpotassium hydroxide, alkali metal or alkaline earth metal carbonatessuch as lithium carbonate, sodium carbonate, potassium carbonate,calcium carbonate or caesium carbonate, if appropriate with addition ofan alkali metal iodide, for example sodium iodide or potassium iodide,alkali alkoxides such as sodium methoxide or potassium methoxide, sodiumethoxide or potassium ethoxide or sodium tert-butoxide or potassiumtert-butoxide, alkali metal hydrides such as sodium hydride orpotassium—hydride, amides such as sodium amide, lithiumbis(trimethylsilyl)amide or potassium bis(trimethylsilyl)-amide orlithium diisopropylamide, or organic amines such as triethylamine,N-methylmorpholine, N-methylpiperidine, N,N-diisopropylethylamine,pyridine, 4-(N,N-dimethylamino)pyridine (DMAP),1,5-diazabicyclo[4.3.0]non-5-ene (DBN),1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) or1,4-diazabicyclo-[2.2.2]octane (DABCO®). Preference is given to usingN,N-diisopropylethylamine

Suitable Broensted acids for the process step (II-A), (II-B) or(II-C)+(III)→(IV-A), (IV-B) or (IV-C) and (II-A), (II-B) or(II-C)+(IX)→(I-A), (I-B) or (I-C), when using approach b) are aqueoushydrochloric acid, hydrobromic acid, hydrochloric acid in dioxane,acetic acid, trifluoroacetic acid, difluoroacetic, p-toluene sulfonicacid, camphor sulfonic acid, methane sulfonic acid, perchloric acid,sulfuric acid, phosphoric acid. Preference is given to hydrochloricacid. Suitable A Lewis acid for this process step is tin chloride.

Suitable bases for the process step (II-A), (II-B) or(II-C)+(III)→(IV-A), (IV-B) or (IV-C) and (II-A), (II-B) or(II-C)+(IX)→(I-A), (I-B) or (I-C), and (IX)+(X)→(XI) when using approachd) and for the process step (IV-A), (IV-B) or (IV-C)+(V)→(I-A), (I-B) or(I-C), and for the process step (VIII)+(III)→(IX) are for example,alkali metal or alkaline earth metal carbonates such as lithiumcarbonate, sodium carbonate, potassium carbonate, calcium carbonate orcaesium carbonate, alkali metal or alkaline earth metal hydroxides suchas sodium hydroxide, potassium hydroxide or barium hydroxide, alkalimetal or alkaline earth metal phosphates such as potassium phosphate,alkali metal alkoxides such as sodium tert-butoxide or potassiumtert-butoxide and sodium methoxide, alkali metal phenoxides such assodium phenoxide, amides such as sodium amide, lithiumbis(trimethylsilyl)amide, sodium bis(trimethylsilyl)amide or potassiumbis(trimethylsilyl)amide or lithium diisopropylamide or organic aminessuch as 1,5-diazabicyclo[4.3.0]non-5-ene (DBN),1,8-diazabicyclo[5.4.0]undec-7-ene (DBU); preference is given to sodiumphenoxide, caesium carbonate, potassium carbonate, sodium tert-butoxideor potassium tert-butoxide or lithium bis(trimethylsilyl)amide.

Suitable inert solvents for the process step (II-A), (II-B) or(II-C)+(III)→(IV-A), (IV-B) or (IV-C) and (IX)+(X)→(XI) for example,when using approach a), b, c) are, aromatic hydrocarbons such asbenzene, toluene or xylene, ethers such as diethyl ether, diisopropylether, methyl tert-butyl ether, 1,2-dimethoxyethane,bis-(2-methoxyethyl) ether, tetrahydrofuran or 1,4-dioxane, or dipolaraprotic solvents such as acetonitrile, N,N-dimethylformamide (DMF),N,N-dimethylacetamide (DMA), dimethyl sulfoxide (DMSO),N,N′-dimethylpropyleneurea (DMPU), N-methylpyrrolidinone (NMP) orpyridine. It is also possible to use mixtures of the solvents mentioned,optionally also in a mixture with water. Preference is given to usingdimethylformamide in a), N-methylpyrrolidinone in b).

Suitable inert solvents for the process step (II-A), (II-B) or(II-C)+(III)→(IV-A), (IV-B) or (IV-C) when using approach d) and for theprocess step (IV-A), (IV-B) or (IV-C)+(V)→(I-A), (I-B) or (I-C) and forthe process steps (IX)+(X)→(XI), (XI)+(XII)→(I-A) and (VIII)+(III)→(IX)are for example, ethers such as 1,4-dioxane, tetrahydrofuran,2-methyltetrahydrofuran, diethyl ether, di-n-butylether, glycol dimethylether or diethylene glycol dimethyl ether, alcohols such as tert-butanolor amyl alcohols or other solvents such as dimethylformamide (DMF),dimethyl sulphoxide (DMSO), dimethylacetamide (DMA), toluene oracetonitrile, or mixtures of the solvents mentioned; preference is givento dimethylformamide, tert-butanol, 1,4-dioxane or toluene.

Suitable Palladium catalysts for the process step (II-A), (II-B) or(II-C)+(III)→(IV-A), (IV-B) or (IV-C) when using approach d) and for theprocess step (IV-A), (IV-B) or (IV-C)+(V)→(I-A), (I-B) or (I-C) and forthe process steps (VIII)+(III)→(IX), (IX)+(X)→(XI) and pay(XII)→(I-A)are, for example, palladium on activated carbon, palladium(II) acetate,bis(dibenzylideneacetone)palladium(0),tetrakis(triphenylphosphine)palladium(0),bis(triphenyl-phosphine)palladium(II) chloride,bis(acetonitrile)palladium(II) chloride and[1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) and thecorresponding dichloromethane complex, optionally in conjunction withadditional phosphane ligands, for example1,4-Bis(diphenylphosphino)butane-palladium(II) chloride (Pd(dppb)Cl₂);Dichloro[1,3-bis(diphenylphosphino)propane]palladium(II) (Pd(dppp)Cl₂),[1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladiu (Pd(dppf)Cl₂,2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (BINAP),(2-biphenyl)di-tert-butylphosphine,dicyclohexyl[2′,4′,6′-tris(1-methylethyl)biphenyl-2-yl]phosphane(XPhos), bis(2-phenylphosphinophenyl) ether (DPEphos) or4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (Xantphos) [cf., forexample, Hassan J. et al., Chem. Rev. 2002, 102, 1359-1469],2-(dicyclohexylphosphine)-3,6-dimethoxy-2′,4′,6′-triisopropyl-1,1′-biphenyl(BrettPhos), 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (SPhos),2-dicyclohexylphosphino-2′,6′-diisopropoxybiphenyl (RuPhos),2-(di-t-butylphosphino)-3-methoxy-6-methyl-2′,4′,6′-tri-i-propyl-1,1′-biphenyl(RockPhos) and 2-di-tert-butylphosphino-2′,4′,6′-triisopropylbiphenyl(tert-ButylXPhos). It is furthermore possible to use appropriateprecatalysts such aschloro-[2-(dicyclohexylphosphine)-3,6-dimethoxy-2′,4′,6′-triisopropyl-1,1′-biphenyl][2-(2-aminoethyp-phenyl]palladium(II) (BrettPhosprecatalyst) [cf., for example, S. L. Buchwald et al., Chem. Sci. 2013,4, 916], optionally in combination with additional phosphane ligandssuch as2-(dicyclohexylphosphine)-3,6-dimethoxy-2′,4′,6′-triisopropyl-1,1′-biphenyl(BrettPhos); preference is given tobis(dibenzylideneacetone)palladium(0) in combination with4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (Xantphos) andchloro-[2-(dicyclohexylphosphine)-3,6-dimethoxy-2′,4′,6′-triisopropyl-1,1′-biphenyl][2-(2-aminoethyl)phenyl]-palladium(II)(BrettPhos precatalyst) or a mixture ofchloro-[2-(dicyclohexylphosphine)-3,6-dimethoxy-2′,4′,6′-triisopropyl-1,1′-biphenyl][2-(2-aminoethyl)phenyl]palladium(II) (BrettPhos precatalyst) and2-(dicyclohexylphosphine)-3,6-dimethoxy-2′,4′,6′-triisopropyl-1,1′-biphenyl(BrettPhos).

The process steps (II-A), (II-B) or (II-C)+(III)→(IV-A), (IV-B) or(IV-C) and (IX)+(X)→(XI) are generally carried out when using approacha) in a temperature range of from −10° C. to +220° C., preferably in a)from +60° C. to +100° C., at atmospheric pressure; in b) and c) from+60° C. to +220° C.; in d) +10° C. to +150° C. However, it is alsopossible to carry out the reaction at reduced or at elevated pressure(for example at from 0.5 to 5 bar). It may optionally be advantageous tocarry out the reaction with microwave irradiation.

The process step (IV-A), (IV-B) or (IV-C)+(V)→(I-A), (I-B) or (I-C) andthe process step (VIII)+(III)→(IX) are generally carried out in atemperature range of from −10° C. to +220° C., preferably in a) from+60° C. to +150° C. However, it is also possible to carry out thereaction at reduced or at elevated pressure (for example at from 0.5 to5 bar). It may optionally be advantageous to carry out the reaction withmicrowave irradiation.

The process step (XI)+(XII)→(I-A) is _(g)enerally carried out in atemperature range of from −20° C. to +250° C., preferably in a) from+80° C. to +150° C. However, it is also possible to carry out thereaction at reduced or at elevated pressure (for example at from 0.5 to5 bar). It may optionally be advantageous to carry out the reaction withmicrowave irradiation.

Suitable inert solvents for the process step (II-A), (II-B) or(II-C)+hydrazine or hydrazine equivalent→(V-A), (V-B) or (V-C) and(IV-A), (IV-B) or (IV-C)+hydrazine or hydrazine equivalent→(V-A), (V-B)or (V-C) and (III)+hydrazine or hydrazine equivalent→(X) are ethers suchas 1,4-dioxane, tetrahydrofuran, 2-methyltetrahydrofuran, diethyl ether,di-n-butylether, glycol dimethyl ether or diethylene glycol dimethylether, alcohols such as tert-butanol or amyl alcohols or other solventssuch as dimethylformamide (DMF), dimethyl sulphoxide (DMSO),dimethylacetamide (DMA), toluene or acetonitrile, or mixtures of thesolvents mentioned; preference is given to dimethylformamide,tert-butanol, 1,4-dioxane or toluene.

The process step (II-A), (II-B) or (II-C)+hydrazine or hydrazineequivalent→(V-A), (V-B) or (V-C) and (IV-A), (IV-B) or (IV-C)+hydrazineor hydrazine equivalent→(V-A), (V-B) or (V-C) and (III)+hydrazine orhydrazine equivalent→(X) is generally carried out in a temperature rangeof from −20° C. to +250° C., preferably in from +50° C. to +120° C., atatmospheric pressure. However, it is also possible to carry out thereaction at reduced or at elevated pressure (for example at from 0.5 to5 bar). It may optionally be advantageous to carry out the reaction withmicrowave irradiation.

Suitable inert solvents for the process step (V-A), (V-B) or(V-C)+(VII)→(I-A), (I-B) or (I-C) and (V-A), (V-B) or (V-C)+(VI)→(I-D),(I-E) or (I-F) and (X)+(VI)→(IX) are ethers such as 1,4-dioxane,tetrahydrofuran, 2-methyltetrahydrofuran, diethyl ether,di-n-butylether, glycol dimethyl ether or diethylene glycol dimethylether, alcohols such as tert-butanol or amyl alcohols or other solventssuch as dimethylformamide (DMF), dimethyl sulphoxide (DMSO),dimethylacetamide (DMA), toluene or acetonitrile, or mixtures of thesolvents mentioned; preference is given to ethanol.

The process step (V-A), (V-B) or (V-C)+(VI)→(I-A), (I-B) or (I-C) and(V-A), (V-B) or (V-C)+(VI)→(I-D), (I-E) or (I-F) and (X)+(VI)→(IX) isgenerally carried out in a temperature range of from −20° C. to +250°C., preferably in from +50° C. to +120° C., at atmospheric pressure.However, it is also possible to carry out the reaction at reduced or atelevated pressure (for example at from 0.5 to 5 bar). It may optionallybe advantageous to carry out the reaction with microwave irradiation.

The compounds of the formula (II-A) and (II-B) are known from theliterature or can be prepared by reacting a compound of the formula(XIII),

in which R⁶ is as defined for the compound of general formula (I) asdefined supra, and

in which R⁹ is as defined for the compound of general formula (I) asdefined supra, and

T² represents chlorine, methoxy, ethoxy or phenoxy

in the presence of a suitable base, with a compound of general formula(XIV),

thereby giving a compound of general formula (XV),

in which R⁶ and R⁶ are as defined for the compound of general formula(I) as defined supra, which is allowed

[G] to react with a hydrazine equivalent, in particular hydrazinemonohydrate, thereby giving a compound of general formula (II-A1),

in which R⁶ and R⁶ are as defined for the compound of general formula(I) as defined supra, or

[H] to react in the presence of a suitable base with dimethyl sulfatethereby giving a compound of general formula (XVI),

in which R⁶ and R⁶ are as defined for the compound of general formula(I) as defined supra, which is then allowed to react with a hydrazineequivalent, in particular hydrazine monohydrate, thereby giving acompound of general formula (II-A1),

in which R⁶ and R⁶ are as defined for the compound of general formula(I) as defined supra, which is then allowed to react with a compound ofgeneral formula (XVII),

in which R³⁶ and R³⁷ are methyl or preferably form a phenyl ringtogether with the atoms they are attached to,

thereby giving a compound of general formula (XVIII-1),

in which R⁵ and R⁶ are as defined for the compound of general formula(I) as defined supra, and R³⁶ and R³⁷ are methyl or preferably form aphenyl ring together with the atoms they are attached to, which is thenin the presence of a suitable base allowed to react with a compound ofgeneral formula (XIX),

in which R⁷ is as defined for the compound of general formula (I) asdefined supra, and

X represents a suitable leaving group, in particular chlorine, bromine,iodine, mesylate, triflate or tosylate,

thereby giving a compound of general formula (XX-1),

in which R⁵, R⁶ and R⁶ are as defined for the compound of generalformula (I) as defined supra, and R³⁶ and R³⁷ are methyl or preferablyform a phenyl ring together with the atoms they are attached to, whichis the allowed to react with a hydrazine equivalent, in particularhydrazine monohydrate.

In the process steps (XV)+hydrazine or hydrazine equivalent→(II-A1) and(XVI)+hydrazine or hydrazine equivalent→(II-A1) the correspondingtautomere (II-B1)

in which R⁹ and R⁸ are as defined for the compound of general formula(I) as defined supra, given that R⁶ is R⁹ and R⁵ is R⁸ is also formed asa person skilled in the art would expect. As a consequence thetautomeres of (XX-1) and (XVIII-1) which are (XVIII-2) and (XX-2),respectively, are formed in the following process steps.

in which R⁹ and R⁸ are as defined for the compound of general formula(I) as defined supra, given that R⁶ is R⁹ and R⁵ is R⁸

The process described is illustrated in an exemplary manner by theschemes below (Scheme 4-6):

[a): LiHMDS, THF, r.t.; b): Hydrazine Monohydrate, EtOH, reflux; c):NaI, DIPEA, DMF, 80° C.; d): DBU, NMP, 190° C.].

[a): Dimethyl sulfate, dioaxne/water, NaHCO₃, reflux b): HydrazineMonohydrate, 2-propanol, reflux].

[a): AcOH, reflux; b): MeI, K₂CO₃, DMF, r.t. c): Hydrazine Monohydrate,EtOH, 80° C.].

The compounds of the formula (II-C) are known from the literature or canbe prepared by reacting a compound of the formula (XXI),

in which R¹¹ and R¹³ are as defined for the compound of general formula(I) as defined supra,

in the presence of a suitable base and in the presenc of a suitablecopper salt with a compound of general formula (XXII),

in which R¹² is as defined for the compound of general formula (I) asdefined supra, and

T³ and T⁴ are defined as hydrogen, methyl or they form a4,4,5,5-tetramethyl-1,3,2-dioxaborolane ring together with the atomsthey are attached to.

thereby giving a compound of general formula (XXIII),

in which R¹¹, R¹² and R¹³ are as defined for the compound of generalformula (I) as defined supra,

which is then hydrogenated in the presence of iron and hydrochloricacid, hydrogen/palladium, iron and ammonium chloride, hydrogen/platiniumdioxide or acetic acid/zinc.

The compounds of the formulae (XIII), (XIV), (XV), (XVII), (XIX), (XXI)and (XXII) are commercially available, known from the literature or canbe prepared analogously to processes known from the literature.

The process described is illustrated in an exemplary manner by thescheme below (Scheme 7):

[a): Cu(OAc)₂, pyridine, DCM, molecular sieves, r.t.; b): Fe, HCl, MeOH,reflux].

Starting materials are either commercially available or can be preparedaccording to procedures available from the public domain, asunderstandable to the person skilled in the art. Specific examples aredescribed in the Experimental Section.

Suitable inert solvents for the process step (XIII)+(XIV)→(XV) forexample, are aromatic hydrocarbons such as benzene, toluene or xylene,ethers such as diethyl ether, diisopropyl ether, methyl tert-butylether, 1,2-dimethoxyethane, bis-(2-methoxyethyl) ether, tetrahydrofuraneor 1,4-dioxane. It is also possible to use mixtures of the solventsmentioned, optionally also in a mixture with water. Preference is givento using tetrahydrofurane in a) ethanol in b).

Suitable bases for the process step (XIII)+(XIV)→(XV) are for example,alkali metal or alkaline earth metal carbonates such as lithiumcarbonate, sodium carbonate, potassium carbonate, calcium carbonate orcaesium carbonate, alkali metal or alkaline earth metal hydroxides suchas sodium hydroxide, potassium hydroxide or barium hydroxide, alkalimetal or alkaline earth metal phosphates such as potassium phosphate,alkali metal alkoxides such as sodium tert-butoxide or potassiumtert-butoxide and sodium methoxide, alkali metal phenoxides such assodium phenoxide, amides such as sodium amide, lithiumbis(trimethylsilyl)amide, sodium bis(trimethylsilyl)amide or potassiumbis(trimethylsilyl)amide or lithium diisopropylamide or organic aminessuch as 1,5-diazabicyclo[4.3.0]non-5-ene (DBN),1,8-diazabicyclo[5.4.0]undec-7-ene (DBU); preference is given to lithiumbis(trimethylsilyl)amide.

The process (XIII)+(XIV)→(XV) is generally carried out in a temperaturerange of from −80° C. to +220° C., preferably in a) from 0° C. to +60°C.

Suitable inert solvents for the process steps (XV)+hydrazine orhydrazine equivalent→(II-Al), (XVI)+hydrazine or hydrazineequivalent→(II-Al) and (XX)+hydrazine or hydrazine equivalent→(II-A) areethers such as 1,4-dioxane, tetrahydrofuran, 2-methyltetrahydrofuran,diethyl ether, di-n-butylether, glycol dimethyl ether or diethyleneglycol dimethyl ether, alcohols such as methanol, ethanol, 2-propanol,tert-butanol or amyl alcohols or other solvents such asdimethylformamide (DMF), dimethyl sulphoxide (DMSO), dimethylacetamide(DMA), toluene or acetonitrile, or mixtures of the solvents mentioned;preference is given to ethanol and 2-propanol.

The process steps (XV)+hydrazine or hydrazine equivalent→(II-Al),(XVI)+hydrazine or hydrazine equivalent→(II-Al) and (XX-1)+hydrazine orhydrazine equivalent→(II-A) are generally carried out in a temperaturerange of from −20° C. to the respective boiling point of the solvent,preferably in from +50° C. to +120° C., at atmospheric pressure.However, it is also possible to carry out the reaction at reduced or atelevated pressure (for example at from 0.5 to 5 bar). It may optionallybe advantageous to carry out the reaction with microwave irradiation.

Suitable inert solvents for the process step (XV)→(XVI) are, aromatichydrocarbons such as benzene, toluene or xylene, ethers such as diethylether, diisopropyl ether, methyl tert-butyl ether, 1,2-dimethoxyethane,bis-(2-methoxyethyl) ether, tetrahydrofuran or 1,4-dioxane, or dipolaraprotic solvents such as acetonitrile, N,N-dimethylformamide (DMF),N,N-dimethylacetamide (DMA), dimethyl sulfoxide (DMSO),N,N′-dimethylpropyleneurea (DMPU), N-methylpyrrolidinone (NMP) orpyridine. It is also possible to use mixtures of the solvents mentioned,optionally also in a mixture with water. Preference is given to using1,4-dioxane or a mixture of 1,4-dioxane and water.

Suitable bases for the process step (XV)→(XVI) are for example, alkalimetal or alkaline earth metal carbonates such as lithium carbonate,sodium carbonate, sodium hydrogen carbonate, potassium carbonate,potassium hydrogen carbonate, calcium carbonate, calcium hydrogencarbonate, or caesium carbonate, alkali metal or alkaline earth metalhydroxides such as sodium hydroxide, potassium hydroxide or bariumhydroxide, alkali metal or alkaline earth metal phosphates such aspotassium phosphate, alkali metal alkoxides such as sodium tert-butoxideor potassium tert-butoxide and sodium methoxide, alkali metal phenoxidessuch as sodium phenoxide, amides such as sodium amide, lithiumbis(trimethylsilyl)amide, sodium bis(trimethylsilyl)amide or potassiumbis(trimethylsilyl)amide or lithium diisopropylamide or organic aminessuch as 1,5-diazabicyclo[4.3.0]non-5-ene (DBN),1,8-diazabicyclo[5.4.0]undec-7-ene (DBU); preference is given to sodiumhydrogen carbonate.

The process step (XV)→(XVI) is generally carried out in a temperaturerange of from −20° C. to to the respective boiling point of the solvent,preferably in from +50° C. to to the respective boiling point of thesolvent, at atmospheric pressure. However, it is also possible to carryout the reaction at reduced or at elevated pressure (for example at from0.5 to 5 bar). It may optionally be advantageous to carry out thereaction with microwave irradiation.

Suitable inert solvents for the process steps (II-Al)+(XVII)>(XVIII) areacids like acetic acid, ethers such as 1,4-dioxane, tetrahydrofuran,2-methyltetrahydrofuran, diethyl ether, di-n-butylether, glycol dimethylether or diethylene glycol dimethyl ether, alcohols such as tert-butanolor amyl alcohols or other solvents such as dimethylformamide (DMF),dimethyl sulphoxide (DMSO), dimethylacetamide (DMA), toluene oracetonitrile, or mixtures of the solvents mentioned; preference is givento acetic acid.

The process step (II-Al)+(XVII)→(XVIII-1) is generally carried out in atemperature range of from −20° C. to to the respective boiling point ofthe solvent, preferably in from +50° C. to +150° C., at atmosphericpressure. However, it is also possible to carry out the reaction atreduced or at elevated pressure (for example at from 0.5 to 5 bar). Itmay optionally be advantageous to carry out the reaction with microwaveirradiation.

Inert solvents for the process step (XVIII-1)+(XIX)→(XX-1) are, forexample, halogenated hydrocarbons such as dichloromethane,trichloromethane, carbon tetrachloride, trichloroethylene orchlorobenzene, ethers such as diethyl ether, dioxane, tetrahydrofuran,glycol dimethyl ether or diethylene glycol dimethyl ether, hydrocarbonssuch as benzene, toluene, xylene, hexane, cyclohexane or mineral oilfractions, or other solvents such as acetone, methyl ethyl ketone, ethylacetate, acetonitrile, N,N-di-methylformamide, N,N-dimethylacetamide,dimethyl sulphoxide, N,N′-dimethylpropyleneurea (DMPU),N-methylpyrrolidone (NMP) or pyridine. It is also possible to usemixtures of the solvents mentioned. Preference is given to usingdimethylformamide or dimethyl sulphoxide.

Suitable bases for the process step (XVIII-1)+(XIX)→(XX-1) are thecustomary inorganic or organic bases. These preferably include alkalimetal hydroxides, for example lithium hydroxide, sodium hydroxide orpotassium hydroxide, alkali metal or alkaline earth metal carbonatessuch as lithium carbonate, sodium carbonate, potassium carbonate,calcium carbonate or caesium carbonate, if appropriate with addition ofan alkali metal iodide, for example sodium iodide or potassium iodide,alkali alkoxides such as sodium methoxide or potassium methoxide, sodiumethoxide or potassium ethoxide or sodium tert-butoxide or potassiumtert-butoxide, alkali metal hydrides such as sodium hydride or potassiumhydride, amides such as sodium amide, lithium bis(trimethylsilyl)amideor potassium bis(trimethylsilyl)amide or lithium diisopropylamide, ororganic amines such as triethylamine, N-methylmorpholine,N-methylpiperidine, N,N-diisopropylethylamine, pyridine,4-(N,N-dimethylamino)pyridine (DMAP), 1,5-diazabicyclo[4.3.0]non-5-ene(DBN), 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) or1,4-diazabicyclo-[2.2.2]octane (DABCO®). Preference is given to usingpotassium carbonate, caesium carbonate or sodium methoxide.

The reaction is generally carried out in a temperature range of from 0°C. to +120° C., preferably at from +20° C. to +80° C., if appropriate ina microwave. The reaction can be carried out at atmospheric, elevated orreduced pressure (for example from 0.5 to 5 bar).

Suitable inert solvents for the process step (XXI)+(XXII)→(XXIII) are,ethers such as diethyl ether, dioxane, tetrahydrofuran, glycol dimethylether or diethylene glycol dimethyl ether, hydrocarbons such as benzene,toluene, xylene, hexane, cyclohexane or mineral oil fractions,halogenated hydrocarbons such as dichloromethane, trichloromethane,carbon tetrachloride, 1,2-dichloroethane, trichloroethylene orchlorobenzene, or other solvents such as acetone, ethyl acetate,acetonitrile, pyridine, dimethyl sulphoxide, N,N-dimethylformamide,N,N-dimethylacetamide, N,N′-dimethylpropyleneurea (DMPU) orN-methylpyrrolidone (NMP). It is also possible to use mixtures of thesolvents mentioned. Preference is given to using dichloromethane.

Suitable bases for the process step (XXI)+(XXII)→(XXIII) are thecustomary inorganic or organic bases. These preferably include alkalimetal hydroxides, for example lithium hydroxide, sodium hydroxide orpotassium hydroxide, alkali metal or alkaline earth metal carbonatessuch as lithium carbonate, sodium carbonate, potassium carbonate,calcium carbonate or caesium carbonate, if appropriate with addition ofan alkali metal iodide, for example sodium iodide or potassium iodide,alkali alkoxides such as sodium methoxide or potassium methoxide, sodiumethoxide or potassium ethoxide or sodium tert-butoxide or potassiumtert-butoxide, alkali metal hydrides such as sodium hydride or potassiumhydride, amides such as sodium amide, lithium bis(trimethylsilyl)amideor potassium bis(trimethylsilyl)amide or lithium diisopropylamide, ororganic amines such as triethylamine, N-methylmorpholine,N-methylpiperidine, N,N-diisopropylethylamine, pyridine,4-(N,N-dimethylamino)pyridine (DMAP), 1,5-diazabicyclo[4.3.0]non-5-ene(DBN), 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) or1,4-diazabicyclo-[2.2.2]octane (DABCO®). Preference is given to usingpyridine

Suitable copper salts for the process step (XXI)+(XXII)→(XXIII) arecopper(II) acetate, copper(I) oxide/oxygen, copper(I) iodide/oxygen,iron and palladium, copper(II) bis(trifluoromethanesulfonate) Preferenceis given to using copper acetate copper acetate.

The reaction is generally carried out in a temperature range of from 0°C. to the respective boiling point of the solvent, preferably from +20°C. to +80° C., if appropriate in a microwave. The reaction can becarried out at atmospheric, elevated or reduced pressure (for examplefrom 0.5 to 5 bar).

Suitable inert solvents for the process steps (XXIII)→(II-C) are etherssuch as 1,4-dioxane, tetrahydrofuran, 2-methyltetrahydrofuran, diethylether, di-n-butylether, glycol dimethyl ether or diethylene glycoldimethyl ether, alcohols such as tert-butanol or amyl alcohols or othersolvents such as dimethylformamide (DMF), dimethyl sulphoxide (DMSO),dimethylacetamide (DMA), toluene or acetonitrile, or mixtures of thesolvents mentioned; preference is given to acetic acid.

The reaction is generally carried out in a temperature range of from 0°C. to the respective boiling point of the solvent, preferably from +20°C. to +100° C., if appropriate in a microwave. The reaction can becarried out at atmospheric, elevated or reduced pressure (for examplefrom 0.5 to 5 bar).

Further compounds according to the invention can optionally also beprepared by converting functional groups of individual substituents, inparticular those listed under R¹, starting with the compounds of theformula (I) obtained by the above processes. These conversions arecarried out by customary methods known to the person skilled in the artand include, for example, reactions such as nucleophilic andelectrophilic substitutions, oxidations, reductions, hydrogenations,transition metal-catalyzed coupling reactions, eliminations, alkylation,amination, esterification, ester cleavage, etherification, ethercleavage, formation of carboxamides, and also the introduction andremoval of temporary protective groups.

The compounds of general formula (I) of the present invention can beconverted to any salt, preferably pharmaceutically acceptable salts, asdescribed herein, by any method which is known to the person skilled inthe art Similarly, any salt of a compound of general formula (I) of thepresent invention can be converted into the free compound, by any methodwhich is known to the person skilled in the art.

Compounds of general formula (I) of the present invention demonstrate avaluable pharmacological spectrum of action which could not have beenpredicted. Compounds of the present invention have surprisingly beenfound to effectively reduce plasma phosphate levels and increase urinaryPi excretion due to their Npt2a inhibition potential. Moreover thecompounds of the present invention have surprisingly been found toeffectively inhibit vascular calcification and to reduce FGF-23 andparathyroid hormone levels significantly by inhibiting Npt2a. It ispossible therefore that said compounds can be used for the treatment orprophylaxis of diseases, preferably soft tissue calcification disordersin humans and animals

Compounds of the present invention can be utilized to prevent and/ortreat diseases and/or conditions associated with hyperphosphatemia,chronic kidney disease (CKD), chronic kidney disease associatedcalcification, non-chronic kidney disease associated calcification,media calcifications including Moenckeberg's medial sclerosis,atherosclerosis, intima calcification, CKD associated heart hypertrophy,CKD associated renal dystrophy, osteoporosis, post-menopausalosteoporosis, diabetes mellitus II, chronic renal disease, aging,hypophosphaturia, hyperparathyroidism, Vitamin D disorders, Vitamin Kdeficiency, Vitamin K-antagonist coagulants, Kawasaki disease, ACDC(arterial calcification due to deficiency of CD73), GACI (generalizedarterial calcification of infancy), IBGC (idiopathic basal gangliacalcification), PXE (pseudoxanthoma elasticum), rheumatoid arthritis,Singleton-Merten syndrome, P-thalassemia, calciphylaxis, heterotrophicossification, preterm placental calcification, calcification of theuterus, calcified uterine fibroids, morbus fahr, mircocalcification andcalcification of the aortic valve. This method comprises administeringto a mammal in need thereof, including a human, an amount of a compoundof this invention, or a pharmaceutically acceptable salt, isomer,polymorph, metabolite, hydrate, solvate or ester thereof; which iseffective to treat the disorder.

The present invention also provides methods of treating diseases and/orconditions associated with hyperphosphatemia, chronic kidney disease(CKD), chronic kidney disease associated calcification, non-chronickidney disease associated calcification, media calcifications includingMoenckeberg's medial sclerosis, atherosclerosis, intima calcification,CKD associated heart hypertrophy, CKD associated renal dystrophy,osteoporosis, post-menopausal osteoporosis, diabetes mellitus II,chronic renal disease, aging, hypophosphaturia, hyperparathyroidism,Vitamin D disorders, Vitamin K deficiency, Vitamin K-antagonistcoagulants, Kawasaki disease, ACDC (arterial calcification due todeficiency of CD73), GACI (generalized arterial calcification ofinfancy), IBGC (idiopathic basal ganglia calcification), PXE(pseudoxanthoma elasticum), rheumatoid arthritis, Singleton-Mertensyndrome, P-thalassemia, calciphylaxis, heterotrophic ossification,preterm placental calcification, calcification of the uterus, calcifieduterine fibroids, morbus fahr, mircocalcification and calcification ofthe aortic valve.

These disorders have been well characterized in humans, but also existwith a similar etiology in other mammals, and can be treated byadministering pharmaceutical compositions of the present invention.

The term “treating” or “treatment” as used in the present text is usedconventionally, e.g., the management or care of a subject for thepurpose of combating, alleviating, reducing, relieving, improving thecondition of a disease or disorder, such as soft tissue calcification,e.g. chronic kidney disease associated calcification, non-chronic kidneydisease associated calcification, and any associated condition.

In accordance with a further aspect, the present invention coverscompounds of general formula (I), as described supra, or stereoisomers,tautomers, hydrates, solvates, and salts thereof, particularlypharmaceutically acceptable salts thereof, or mixtures of same, for usein the treatment and/or prophylaxis of diseases.

In accordance with a further embodiment, the present invention coverscompounds of general formula (I), as described supra, or stereoisomers,tautomers, hydrates, solvates, and salts thereof, particularlypharmaceutically acceptable salts thereof, or mixtures of same, for usein the treatment and/or prophylaxis of diseases and/or conditionsassociated with hyperphosphatemia, chronic kidney disease (CKD), chronickidney disease associated calcification, non-chronic kidney diseaseassociated calcification, media calcifications including Moenckeberg'smedial sclerosis, atherosclerosis, intima calcification, CKD associatedheart hypertrophy, CKD associated renal dystrophy, osteoporosis,post-menopausal osteoporosis, diabetes mellitus II, chronic renaldisease, aging, hypophosphaturia, hyperparathyroidism, Vitamin Ddisorders, Vitamin K deficiency, Vitamin K-antagonist coagulants,Kawasaki disease, ACDC (arterial calcification due to deficiency ofCD73), GACI (generalized arterial calcification of infancy), IBGC(idiopathic basal ganglia calcification), PXE (pseudoxanthomaelasticum), rheumatoid arthritis, Singleton-Merten syndrome,P-thalassemia, calciphylaxis, heterotrophic ossification, pretermplacental calcification, calcification of the uterus, calcified uterinefibroids, morbus fahr, mircocalcification and calcification of theaortic valve.

The pharmaceutical activity of the compounds according to the inventioncan be explained by their activity as Npt2a Inhibitors.

In accordance with a further aspect, the present invention covers theuse of compounds of general formula (I), as described supra, orstereoisomers, tautomers, hydrates, solvates, and salts thereof,particularly pharmaceutically acceptable salts thereof, or mixtures ofsame, for the treatment and/or prophylaxis of diseases, in particulardiseases and/or conditions associated with hyperphosphatemia, chronickidney disease (CKD), chronic kidney disease associated calcification,non-chronic kidney disease associated calcification, mediacalcifications including Moenckeberg's medial sclerosis,atherosclerosis, intima calcification, CKD associated heart hypertrophy,CKD associated renal dystrophy, osteoporosis, post-menopausalosteoporosis, diabetes mellitus II, chronic renal disease, aging,hypophosphaturia, hyperparathyroidism, Vitamin D disorders, Vitamin Kdeficiency, Vitamin K-antagonist coagulants,

Kawasaki disease, ACDC (arterial calcification due to deficiency ofCD73), GACI (generalized arterial calcification of infancy), IBGC(idiopathic basal ganglia calcification), PXE (pseudoxanthomaelasticum), rheumatoid arthritis, Singleton-Merten syndrome,P-thalassemia,calciphylaxis, heterotrophic ossification, pretermplacental calcification, calcification of the uterus, calcified uterinefibroids, morbus fahr, mircocalcification and calcification of theaortic valve.

In accordance with a further aspect, the present invention covers theuse of compounds of general formula (I), as described supra, orstereoisomers, tautomers, hydrates, solvates, and salts thereof,particularly pharmaceutically acceptable salts thereof, or mixtures ofsame, in a method of treatment and/or prophylaxis of diseases, inparticular diseases and/or conditions associated with hyperphosphatemia,chronic kidney disease (CKD), chronic kidney disease associatedcalcification, non-chronic kidney disease associated calcification,media calcifications including Moenckeberg's medial sclerosis,atherosclerosis, intima calcification, CKD associated heart hypertrophy,CKD associated renal dystrophy, osteoporosis, post-menopausalosteoporosis, diabetes mellitus II, chronic renal disease, aging,hypophosphaturia, hyperparathyroidism, Vitamin D disorders, Vitamin Kdeficiency, Vitamin K-antagonist coagulants, Kawasaki disease, ACDC(arterial calcification due to deficiency of CD73), GACI (generalizedarterial calcification of infancy), IBGC (idiopathic basal gangliacalcification), PXE (pseudoxanthoma elasticum), rheumatoid arthritis,Singleton-Merten syndrome, P-thalassemia, calciphylaxis, heterotrophicossification, preterm placental calcification, calcification of theuterus, calcified uterine fibroids, morbus fahr, mircocalcification andcalcification of the aortic valve.

In accordance with a further aspect, the present invention covers theuse of a compound of general formula (I), as described supra, orstereoisomers, tautomers, hydrates, solvates, and salts thereof,particularly pharmaceutically acceptable salts thereof, or mixtures ofsame, for the preparation of a pharmaceutical composition, preferably amedicament, for the treatment and/or prophylaxis of diseases, indiseases and/or conditions associated with hyperphosphatemia, chronickidney disease (CKD), chronic kidney disease associated calcification,non-chronic kidney disease associated calcification, mediacalcifications including Moenckeberg's medial sclerosis,atherosclerosis, intima calcification, CKD associated heart hypertrophy,CKD associated renal dystrophy, osteoporosis, post-menopausalosteoporosis, diabetes mellitus II, chronic renal disease, aging,hypophosphaturia, hyperparathyroidism, Vitamin D disorders, Vitamin Kdeficiency, Vitamin K-antagonist coagulants, Kawasaki disease, ACDC(arterial calcification due to deficiency of CD73), GACI (generalizedarterial calcification of infancy), IBGC (idiopathic basal gangliacalcification), PXE (pseudoxanthoma elasticum), rheumatoid arthritis,Singleton-Merten syndrome, P-thalassemia,calciphylaxis, heterotrophicossification, preterm placental calcification, calcification of theuterus, calcified uterine fibroids, morbus fahr, mircocalcification andcalcification of the aortic valve.

In accordance with a further aspect, the present invention covers amethod of treatment and/or prophylaxis of diseases, in diseases and/orconditions associated with hyperphosphatemia, chronic kidney disease(CKD), chronic kidney disease associated calcification, non-chronickidney disease associated calcification, media calcifications includingMoenckeberg's medial sclerosis, atherosclerosis, intima calcification,CKD associated heart hypertrophy, CKD associated renal dystrophy,osteoporosis, post-menopausal osteoporosis, diabetes mellitus II,chronic renal disease, aging, hypophosphaturia, hyperparathyroidism,Vitamin D disorders, Vitamin K deficiency, Vitamin K-antagonistcoagulants, Kawasaki disease, ACDC (arterial calcification due todeficiency of CD73), GACI (generalized arterial calcification ofinfancy), IBGC (idiopathic basal ganglia calcification), PXE(pseudoxanthoma elasticum), rheumatoid arthritis, Singleton-Mertensyndrome, P-thalassemia,calciphylaxis, heterotrophic ossification,preterm placental calcification, calcification of the uterus, calcifieduterine fibroids, morbus fahr, mircocalcification and calcification ofthe aortic valve, using an effective amount of a compound of generalformula (I), as described supra, or stereoisomers, tautomers, hydrates,solvates, and salts thereof, particularly pharmaceutically acceptablesalts thereof, or mixtures of same.

In accordance with a further aspect, the present invention coverspharmaceutical compositions, in particular a medicament, comprising acompound of general formula (I), as described supra, or a stereoisomer,a tautomer, an N-oxide, a hydrate, a solvate, a salt thereof,particularly a pharmaceutically acceptable salt, or a mixture of same,and one or more excipients, in particular one or more pharmaceuticallyacceptable excipient(s). Conventional procedures for preparing suchpharmaceutical compositions in appropriate dosage forms can be utilized.

The present invention furthermore covers pharmaceutical compositions, inparticular medicaments, which comprise at least one compound accordingto the invention, conventionally together with one or morepharmaceutically suitable excipients, and to their use for the abovementioned purposes.

The compounds of general formula (I), as described supra, orstereoisomers, tautomers, hydrates, solvates, and salts thereof,particularly pharmaceutically acceptable salts thereof, or mixtures ofsame, are suitable for the treatment and/or prophylaxis of diseasesand/or conditions associated with hyperphosphatemia, chronic kidneydisease (CKD), chronic kidney disease associated calcification,non-chronic kidney disease associated calcification, mediacalcifications including Moenckeberg's medial sclerosis,atherosclerosis, intima calcification, CKD associated heart hypertrophy,CKD associated renal dystrophy, osteoporosis, post-menopausalosteoporosis, diabetes mellitus II, chronic renal disease, aging,hypophosphaturia, hyperparathyroidism, Vitamin D disorders, Vitamin Kdeficiency, Vitamin K-antagonist coagulants, Kawasaki disease, ACDC(arterial calcification due to deficiency of CD73), GACI (generalizedarterial calcification of infancy), IBGC (idiopathic basal gangliacalcification), PXE (pseudoxanthoma elasticum), rheumatoid arthritis,Singleton-Merten syndrome, P-thalassemia, calciphylaxis, heterotrophicossification, preterm placental calcification, calcification of theuterus, calcified uterine fibroids, morbus fahr, mircocalcification andcalcification of the aortic valve. The compounds of general formula (I),as described supra, or stereoisomers, tautomers, hydrates, solvates, andsalts thereof, particularly pharmaceutically acceptable salts thereof,or mixtures of same, are also suitable for the treatment and/orprophylaxis of chronic kidney disease (CKD).The compounds of generalformula (I), as described supra, or stereoisomers, tautomers, hydrates,solvates, and salts thereof, particularly pharmaceutically acceptablesalts thereof, or mixtures of same, are also suitable for the treatmentand/or prophylaxis of soft tissue calcification disorders. The compoundsof general formula (I), as described supra, or stereoisomers, tautomers,hydrates, solvates, and salts thereof, particularly pharmaceuticallyacceptable salts thereof, or mixtures of same, are also suitable for thetreatment and/or prophylaxis of chronic kidney disease associatedcalcification disorders and non-chronic kidney disease associatedcalcification disorders.

The compounds of general formula (I), as described supra, orstereoisomers, tautomers, hydrates, solvates, and salts thereof,particularly pharmaceutically acceptable salts thereof, or mixtures ofsame, are suitable for the treatment and/or prophylaxis ofcardiovascular and of renal disorders, in particular of diseases and/orconditions associated with hyperphosphatemia, soft tissue calcification,chronic kidney disease (CKD), soft tissue calcification, in particularchronic kidney disease associated calcification and non-chronic kidneydisease associated calcification, and also of chronic renal disease,.

Within the meaning of the present invention, the term renalinsufficiency comprises both acute and chronic manifestations of renalinsufficiency, and also underlying or related renal disorders such asdiabetic and non-diabetic nephropathies, hypertensive nephropathies,ischaemic renal disorders, renal hypoperfusion, intradialytichypotension, obstructive uropathy, renal stenoses, glomerulopathies,glomerulonephritis (such as, for example, primary glomerulonephritides;minimal change glomerulonephritis (lipoidnephrosis); membranousglomerulonephritis; focal segmental glomerulosclerosis (FSGS);

membrane-proliferative glomerulonephritis; crescenticglomerulonephritis; me sangioproliferative glomerulonephritis (IgAnephritis, Berger's disease); post-infectious glomerulonephritis;secondary glomerulonephritides: diabetes mellitus, lupus erythematosus,amyloidosis, Goodpasture syndrome, Wegener granulomatosis,Henoch-Schnlein purpura, microscopic polyangiitis, acuteglomerulonephritis, pyelonephritis (for example as a result of:urolithiasis, benign prostate hyperplasia, diabetes, malformations,abuse of analgesics, Crohn's disease), glomerulosclerosis,arteriolonecrose of the kidney, tubulointerstitial diseases,nephropathic disorders such as primary and congenital or aquired renaldisorder, Alport syndrome, nephritis, immunological kidney disorderssuch as kidney transplant rejection and immunocomplex-induced renaldisorders, nephropathy induced by toxic substances, nephropathy inducedby contrast agents, diabetic and non-diabetic nephropathy, renal cysts,nephrosclerosis, hypertensive nephrosclerosis and nephrotic syndromewhich can be characterized diagnostically, for example by abnormallyreduced creatinine and/or water excretion, abnormally elevated bloodconcentrations of urea, nitrogen, potassium and/or creatinine, alteredactivity of renal enzymes, for example glutamyl synthetase, alteredurine osmolarity or urine volume, elevated microalbuminuria,macroalbuminuria, lesions on glomerulae and arterioles, tubulardilatation, hyperphosphataemia and/or the need for dialysis. The presentinvention also comprises the use of the compounds according to theinvention for the treatment and/or prophylaxis of sequelae of renalinsufficiency, for example pulmonary oedema, heart failure, uremia,anemia, electrolyte disturbances (for example hypercalemia,hyponatremia) and disturbances in bone and carbohydrate metabolism.

The compounds of general formula (I), as described supra, orstereoisomers, tautomers, hydrates, solvates, and salts thereof,particularly pharmaceutically acceptable salts thereof, or mixtures ofsame, can also be used for the treatment and/or prophylaxis of sequelaeof renal insufficiency, for example pulmonary oedema, heart failure,uraemia, anaemia, electrolyte disturbances (for example hyperkalaemia,hyponatraemia) and disturbances in bone and carbohydrate metabolism.

The compounds of general formula (I), as described supra, orstereoisomers, tautomers, hydrates, solvates, and salts thereof,particularly pharmaceutically acceptable salts thereof, or mixtures ofsame, can also be used for the treatment and/or prophylaxis of metabolicsyndrome, hypertension, resistant hypertension, acute and chronic heartfailure, coronary heart disease, stable and unstable angina pectoris,peripheral and cardiac vascular disorders, for treatment and/orprophylaxis of thromboembolic disorders and ischaemias such asmyocardial ischaemia, myocardial infarction, stroke, cardiachypertrophy, transient and ischaemic attacks, preeclampsia, inflammatorycardiovascular disorders, spasms of the coronary arteries and peripheralarteries, oedema formation, for example pulmonary oedema, cerebraloedema, renal oedema or oedema caused by heart failure, peripheralcirculatory disturbances, reperfusion damage, arterial and venousthromboses, myocardial insufficiency, endothelial dysfunction, toprevent restenoses, for example after thrombolysis therapies,percutaneous transluminal angioplasties (PTA), transluminal coronaryangioplasties (PTCA), heart transplants and bypass operations, and alsomicro- and macrovascular damage (vasculitis), increased levels offibrinogen and of low-density lipoprotein (LDL) and increasedconcentrations of plasminogen activator inhibitor 1 (PAI-1), and alsofor treatment and/or prophylaxis of erectile dysfunction and femalesexual dysfunction.

The compounds of general formula (I), as described supra, orstereoisomers, tautomers, hydrates, solvates, and salts thereof,particularly pharmaceutically acceptable salts thereof, or mixtures ofsame, can also be used for the treatment and/or prophylaxis of pulmonaryarterial hypertension (PAH) and other forms of pulmonary hypertension(PH) including left-heart disease, thromboembolisms (CTEPH),sarcoidosis, COPD or pulmonary fibrosis-associated pulmonaryhypertension, chronic-obstructive pulmonary disease (COPD).

Due to their activity and selectivity profile, the compounds of generalformula (I), as described supra, or stereoisomers, tautomers, hydrates,solvates, and salts thereof, particularly pharmaceutically acceptablesalts thereof, or mixtures of same, are believed to be particularlysuitable for the treatment and/or prevention preeclampsia, peripheralarterial disease (PAD) and coronary microvascular dysfunction (CMD),Raynaud's syndrome, dy smenorrhe a, glaucoma, diabetic retinopathy,proliferative vitroretinopathy and disorders of the connective tissue(for example sarcoidosisdiabetic, inflammatory or hypertensivenephropaties, fibrotic disorders, cardiac insufficiency, anginapectoris, hypertension, ischemias, vascular disorders, thromboembolicdisorders, erectile dysfunction, dementia and Alzheimer.

The compounds of general formula (I), as described supra, orstereoisomers, tautomers, hydrates, solvates, and salts thereof,particularly pharmaceutically acceptable salts thereof, or mixtures ofsame, are suitable in particular for improving perception,concentration, learning or memory after cognitive impairments like thoseoccurring in particular in association withsituations/diseases/syndromes such as mild cognitive impairment,age-associated learning and memory impairments, age-associated memorylosses, vascular dementia, craniocerebral trauma, stroke, dementiaoccurring after strokes (post stroke dementia), post-traumaticcraniocerebral trauma, general concentration impairments, concentrationimpairments in children with learning and memory problems.

The compounds of general formula (I), as described supra, orstereoisomers, tautomers, hydrates, solvates, and salts thereof,particularly pharmaceutically acceptable salts thereof, or mixtures ofsame, are furthermore also suitable for controlling cerebral blood flowand thus represent effective agents for controlling migraines. They arealso suitable for the prophylaxis and control of sequelae of cerebralinfarction (cerebral apoplexy) such as stroke, cerebral ischaemia andcraniocerebral trauma. The compounds according to the invention canlikewise be used for controlling states of pain and tinnitus.

The present invention further provides a method for treatment and/orprophylaxis of disorders, in particular the disorders mentioned above,using an effective amount of at least one of the compounds according tothe invention.

It is possible for the compounds according to the invention to havesystemic and/or local activity. For this purpose, they can beadministered in a suitable manner, such as, for example, via the oral,parenteral, pulmonary, nasal, sublingual, lingual, buccal, rectal,vaginal, dermal, transdermal, conjunctival, otic route or as an implantor stent.

For these administration routes, it is possible for the compoundsaccording to the invention to be administered in suitable administrationforms.

For oral administration, it is possible to formulate the compoundsaccording to the invention to dosage forms known in the art that deliverthe compounds of the invention rapidly and/or in a modified manner, suchas, for example, tablets (uncoated or coated tablets, for example withenteric or controlled release coatings that dissolve with a delay or areinsoluble), orally-disintegrating tablets, films/wafers,films/lyophylisates, capsules (for example hard or soft gelatinecapsules), sugar-coated tablets, granules, pellets, powders, emulsions,suspensions, aerosols or solutions. It is possible to incorporate thecompounds according to the invention in crystalline and/or amorphisedand/or dissolved form into said dosage forms.

Parenteral administration can be effected with avoidance of anabsorption step (for example intravenous, intraarterial, intracardial,intraspinal or intralumbal) or with inclusion of absorption (for exampleintramuscular, subcutaneous, intracutaneous, percutaneous orintraperitoneal). Administration forms which are suitable for parenteraladministration are, inter alia, preparations for injection and infusionin the form of solutions, suspensions, emulsions, lyophylisates orsterile powders.

Examples which are suitable for other administration routes arepharmaceutical forms for inhalation [inter alia powder inhalers,nebulizers], nasal drops, nasal solutions, nasal sprays;tablets/films/wafers/capsules for lingual, sublingual or buccaladministration; suppositories; eye drops, eye ointments, eye baths,ocular inserts, ear drops, ear sprays, ear powders, ear-rinses, eartampons; vaginal capsules, aqueous suspensions (lotions, mixturaeagitandae), lipophilic suspensions, emulsions, ointments, creams,transdermal therapeutic systems (such as, for example, patches), milk,pastes, foams, dusting powders, implants or stents.

The compounds according to the invention can be incorporated into thestated administration forms. This can be effected in a manner known perse by mixing with pharmaceutically suitable excipients. Pharmaceuticallysuitable excipients include, inter alia,

fillers and carriers (for example cellulose, microcrystalline cellulose(such as, for example, Avicel®), lactose, mannitol, starch, calciumphosphate (such as, for example, Di-Cafos®)),

ointment bases (for example petroleum jelly, paraffins, triglycerides,waxes, wool wax, wool wax alcohols, lanolin, hydrophilic ointment,polyethylene glycols),

bases for suppositories (for example polyethylene glycols, cacao butter,hard fat),

solvents (for example water, ethanol, isopropanol, glycerol, propyleneglycol, medium chain-length triglycerides fatty oils, liquidpolyethylene glycols, paraffins),

surfactants, emulsifiers, dispersants or wetters (for example sodiumdodecyl sulfate), lecithin, phospholipids, fatty alcohols (such as, forexample, Lanette®), sorbitan fatty acid esters (such as, for example,Span®), polyoxyethylene sorbitan fatty acid esters (such as, forexample, Tween®), polyoxyethylene fatty acid glycerides (such as, forexample, Cremophor®), polyoxethylene fatty acid esters, polyoxyethylenefatty alcohol ethers, glycerol fatty acid esters, poloxamers (such as,for example, Pluronic®),

buffers, acids and bases (for example phosphates, carbonates, citricacid, acetic acid, hydrochloric acid, sodium hydroxide solution,ammonium carbonate, trometamol, triethanolamine),

isotonicity agents (for example glucose, sodium chloride),

adsorbents (for example highly-disperse silicas),

viscosity-increasing agents, gel formers, thickeners and/or binders (forexample polyvinylpyrrolidone, methylcellulose,hydroxypropylmethylcellulose, hydroxypropylcellulose,carboxymethylcellulose-sodium, starch, carbomers, polyacrylic acids(such as, for example, Carbopol®); alginates, gelatine),

disintegrants (for example modified starch,carboxymethylcellulose-sodium, sodium starch glycolate (such as, forexample, Explotab®), cross-linked polyvinylpyrrolidone,croscarmellose-sodium (such as, for example, AcDiSol®)),

flow regulators, lubricants, glidants and mould release agents (forexample magnesium stearate, stearic acid, talc, highly-disperse silicas(such as, for example, Aerosil®)),

coating materials (for example sugar, shellac) and film formers forfilms or diffusion membranes which dissolve rapidly or in a modifiedmanner (for example polyvinylpyrrolidones (such as, for example,Kollidon®), polyvinyl alcohol, hydroxypropylmethylcellulose,hydroxypropylcellulose, ethylcellulose, hydroxypropylmethylcellulosephthalate, cellulose acetate, cellulose acetate phthalate,polyacrylates, polymethacrylates such as, for example, Eudragit®)),

capsule materials (for example gelatine, hydroxypropylmethylcellulose),

synthetic polymers (for example polylactides, polyglycolides,polyacrylates, polymethacrylates (such as, for example, Eudragit®),polyvinylpyrrolidones (such as, for example, Kollidon®), polyvinylalcohols, polyvinyl acetates, polyethylene oxides, polyethylene glycolsand their copolymers and blockcopolymers),

plasticizers (for example polyethylene glycols, propylene glycol,glycerol, triacetine, triacetyl citrate, dibutyl phthalate),

penetration enhancers,

stabilisers (for example antioxidants such as, for example, ascorbicacid, ascorbyl palmitate, sodium ascorbate, butylhydroxyanisole,butylhydroxytoluene, propyl gallate),

preservatives (for example parabens, sorbic acid, thiomersal,benzalkonium chloride, chlorhexidine acetate, sodium benzoate),

colourants (for example inorganic pigments such as, for example, ironoxides, titanium dioxide),

flavourings, sweeteners, flavour- and/or odour-masking agents.

The present invention furthermore relates to a pharmaceuticalcomposition which comprise at least one compound according to theinvention, conventionally together with one or more pharmaceuticallysuitable excipient(s), and to their use according to the presentinvention.

In accordance with another aspect, the present invention coverspharmaceutical combinations, in particular medicaments, comprising atleast one compound of general formula (I) of the present invention andat least one or more further active ingredients, in particular for thetreatment and/or prophylaxis of diseases and/or conditions associatedwith hyperphosphatemia, chronic kidney disease (CKD), soft tissuecalcification, chronic kidney disease associated calcification,non-chronic kidney disease associated calcification, mediacalcifications including Moenckeberg's medial sclerosis,atherosclerosis, intima calcification, CKD associated heart hypertrophy,CKD associated renal dystrophy, osteoporosis, post-menopausalosteoporosis, diabetes mellitus II, chronic renal disease, aging,hypophosphaturia, hyperparathyroidism, Vitamin D disorders, Vitamin Kdeficiency, Vitamin K-antagonist coagulants, Kawasaki disease, ACDC(arterial calcification due to deficiency of CD73), GACI (generalizedarterial calcification of infancy), IBGC (idiopathic basal gangliacalcification), PXE (pseudoxanthoma elasticum), rheumatoid arthritis,Singleton-Merten syndrome, P-thalassemia,calciphylaxis, heterotrophicossification, preterm placental calcification, calcification of theuterus, calcified uterine fibroids, morbus fahr, mircocalcification andcalcification of the aortic valve.

An embodiment of the invention are pharmaceutical compositionscomprising at least one compound of formula (I) according to theinvention, preferably together with at least one inert, non-toxic,pharmaceutically suitable auxiliary, and the use of these pharmaceuticalcompositions for the above cited purposes.

Particularly, the present invention covers a pharmaceutical combination,which comprises:

one or more first active ingredients, in particular compounds of generalformula (I) as defined supra, and one or more further activeingredients, in particular for the treatment and/or prophylaxis ofdiseases and/or conditions associated with hyperphosphatemia, chronickidney disease (CKD), soft tissue calcification, chronic kidney diseaseassociated calcification, non-chronic kidney disease associatedcalcification, media calcifications including Moenckeberg's medialsclerosis, atherosclerosis, intima calcification, CKD associated hearthypertrophy, CKD associated renal dystrophy, osteoporosis,post-menopausal osteoporosis, diabetes mellitus II, chronic renaldisease, aging, hypophosphaturia ,hyperparathyroidism, Vitamin Ddisorders, Vitamin K deficiency, Vitamin K-antagonist coagulants,Kawasaki disease, ACDC (arterial calcification due to deficiency ofCD73), GACI (generalized arterial calcification of infancy), IBGC(idiopathic basal ganglia calcification), PXE (pseudoxanthomaelasticum), rheumatoid arthritis, Singleton-Merten syndrome,P-thalassemia,calciphylaxis, heterotrophic ossification, pretermplacental calcification, calcification of the uterus, calcified uterinefibroids, morbus fahr, mircocalcification and calcification of theaortic valve.

The term “combination” in the present invention is used as known topersons skilled in the art, it being possible for said combination to bea fixed combination, a non-fixed combination or a kit-of-parts.

A “fixed combination” in the present invention is used as known topersons skilled in the art and is defined as a combination wherein, forexample, a first active ingredient, such as one or more compounds ofgeneral formula (I) of the present invention, and a further activeingredient are present together in one unit dosage or in one singleentity. One example of a “fixed combination” is a pharmaceuticalcomposition wherein a first active ingredient and a further activeingredient are present in admixture for simultaneous administration,such as in a formulation. Another example of a “fixed combination” is apharmaceutical combination wherein a first active ingredient and afurther active ingredient are present in one unit without being inadmixture.

A non-fixed combination or “kit-of-parts” in the present invention isused as known to persons skilled in the art and is defined as acombination wherein a first active ingredient and a further activeingredient are present in more than one unit. One example of a non-fixedcombination or kit-of-parts is a combination wherein the first activeingredient and the further active ingredient are present separately. Itis possible for the components of the non-fixed combination orkit-of-parts to be administered separately, sequentially,simultaneously, concurrently or chronologically staggered.

The compounds of the present invention can be administered as the solepharmaceutical agent or in combination with one or more otherpharmaceutically active ingredients where the combination causes nounacceptable adverse effects. The present invention also covers suchpharmaceutical combinations. For example, the compounds of the presentinvention can be combined with known agents of the same indicationtreatment group, such as agents used for the treatment and/orprophylaxis of diseases and/or conditions associated withhyperphosphatemia, elevated plasma FGF23 levels, chronic kidney disease(CKD), soft tissue calcification, chronic kidney disease associatedcalcification, non-chronic kidney disease associated calcification,media calcifications including Moenckeberg's medial sclerosis,atherosclerosis, intima calcification, CKD associated heart hypertrophy,CKD associated renal dystrophy, osteoporosis, post-menopausalosteoporosis, diabetes mellitus II, chronic renal disease, aging,hypophosphaturia ,hyperparathyroidism, Vitamin D disorders, Vitamin Kdeficiency, Vitamin K-antagonist coagulants, Kawasaki disease, ACDC(arterial calcification due to deficiency of CD73), GACI (generalizedarterial calcification of infancy), IBGC (idiopathic basal gangliacalcification), PXE (pseudoxanthoma elasticum), rheumatoid arthritis,Singleton-Merten syndrome, P-thalassemia, calciphylaxis, heterotrophicossification, preterm placental calcification, calcification of theuterus, calcified uterine fibroids, morbus fahr, mircocalcification andcalcification of the aortic valve.

The inventive compounds can be employed alone or, if required, incombination with other active ingredients. The present invention furtherprovides medicaments comprising at least one of the inventive compoundsand one or more further active ingredients, especially for treatmentand/or prophylaxis of the aforementioned disorders. Preferred examplesof suitable active ingredient combinations include:

organic nitrates and NO donors, for example sodium nitroprusside,nitroglycerin, isosorbide mononitrate, isosorbide dinitrate, molsidomineor SIN-1, and inhaled NO;

compounds which inhibit the breakdown of cyclic guanosine monophosphate(cGMP), for example inhibitors of phosphodiesterases (PDE) 1, 2 and/or5, especially PDE 5 inhibitors such as sildenafil, vardenafil,tadalafil, udenafil, desantafil, avanafil, mirodenafil, lodenafil orPF-00489791;

antithrombotic agents, by way of example and with preference from thegroup of the platelet aggregation inhibitors, the anticoagulants or theprofibrinolytic substances;

hypotensive active ingredients, by way of example and with preferencefrom the group of the calcium antagonists, angiotensin All antagonists,ACE inhibitors, NEP-inhibitors, vasopeptidase-inhibitors, endothelinantagonists, renin inhibitors, alpha-receptor blockers, beta-receptorblockers, mineralocorticoid receptor antagonists, rho-kinase-inhibitorsand the diuretics;

antiarrhythmic agents, by way of example and with preference from thegroup of sodium channel blocker, beta-receptor blocker, potassiumchannel blocker, calcium antagonists, If-channel blocker, digitalis,parasympatholytics (vagoliytics), sympathomimetics and otherantiarrhythmics as adenosin, adenosine receptor agonists as well asvernakalant;

positive-inotrop agents, by way of example cardiac glycoside (Dogoxin),beta-adrenergic and dopaminergic agonists, such as isoprenalin,adrenalin, noradrenalin, dopamin or dobutamin;

vasopressin-rezeptor-antagonists, by way of example and with preferencefrom the group of conivaptan, tolvaptan, lixivaptan, mozavaptan,satavaptan, SR-121463, RWJ 676070 or BAY 86-8050, as well as thecompounds described in WO 2010/105770, WO2011/104322 and WO 2016/071212;

active ingredients which alter lipid metabolism, for example and withpreference from the group of the thyroid receptor agonists, cholesterolsynthesis inhibitors such as, by way of example and preferably, HMG-CoAreductase inhibitors or squalene synthesis inhibitors, of ACATinhibitors, CETP inhibitors, MTP inhibitors, PPAR-alpha, PPAR-gammaand/or PPAR-delta agonists, cholesterol absorption inhibitors, lipaseinhibitors, polymeric bile acid adsorbents, bile acid reabsorptioninhibitors and lipoprotein(a) antagonists.

bronchodilatory agents, for example and with preference from the groupof the beta-adrenergic rezeptor-agonists, such as, by way of example andpreferably, albuterol, isoproterenol, metaproterenol, terbutalin,formoterol or salmeterol, or from the group of the anticholinergics,such as, by way of example and preferably, ipratropiumbromid;

anti-inflammatory agents, for example and with preference from the groupof the glucocorticoids, such as, by way of example and preferably,prednison, prednisolon, methylprednisolon, triamcinolon, dexamethason,beclomethason, betamethason, flunisolid, budesonid or fluticason as wellas the non-steroidal anti-inflammatory agents (NSAIDs), by way ofexample and preferably, acetyl salicylic acid (aspirin), ibuprofen andnaproxen, 5-amino salicylic acid-derivates, leukotriene-antagonists,TNF-alpha-inhibitors and chemokin-receptor antagonists, such as CCR1, 2and/or 5 inhibitors;

agents that inhibit the signal transductions cascade, for example andwith preference from the group of the kinase inhibitors, by way ofexample and preferably, from the group of the tyrosine kinase- and/orserine/threonine kinase inhibitors;

agents, that inhibit the degradation and modification of theextracellular matrix, for example and with preference from the group ofthe inhibitors of the matrix-metalloproteases (MMPs), by way of exampleand preferably, inhibitors of chymasee, stromely sine, collagenases,gelatinases and aggrecanases (with preference from the group of MMP-1,MMP-3, MMP-8, MMP-9, MMP-10, MMP-11 and MMP-13) as well as of themetallo-elastase (MMP-12) and neutrophil-elastase (HNE), as for examplesivelestat or DX-890;

agents, that block the bindung of serotonin to its receptor, for exampleand with preference antagonists of the 5-HT_(2b)-receptor;

organic nitrates and NO-donators, for example and with preference sodiumnitroprussid, nitroglycerine, isosorbid mononitrate, isosorbiddinitrate, molsidomine or SIN-1, as well as inhaled NO;

NO-independent, but heme-dependent stimulators of the soluble guanylatecyclase, for example and with preference the compounds described in WO00/06568, WO 00/06569, WO 02/42301, WO 03/095451, WO 2011/147809, WO2012/004258, WO 2012/028647 and WO 2012/059549;

NO-independent and heme-independent activators of the soluble guanylatecyclase, for example and with preference the compounds described in WO01/19355, WO 01/19776, WO 01/19778, WO 01/19780, WO 02/070462 and WO02/070510 beschriebenen Verbindungen;

agents, that stimulates the synthesis of cGMP, wie beispielsweise sGCModulatoren, for example and with preference riociguat, cinaciguat,vericiguat or BAY 1101042;

prostacyclin-analogs, for example and with preference iloprost,beraprost, treprostinil or epoprostenol;

agents, that inhibit soulble epoxidhydrolase (sEH), for example and withpreference N,N′-Dicyclohexyl urea, 12-(3-Adamantan-1-yl-ureido)-dodecanic acid or1-Adamantan-1-yl-3-{5-[2-(2-ethoxyethoxy)ethoxy]pentyl}-urea;

agents that interact with glucose metabolism, for example and withpreference insuline, biguanide, thiazolidinedione, sulfonyl urea,acarbose, DPP4 inhibitors, GLP-1 analogs or SGLT-1 inhibitors;

natriuretic peptides, for example and with preference atrial natriureticpeptide (ANP), natriuretic peptide type B (BNP, Nesiritid) natriureticpeptide type C (CNP) or urodilatin;

activators of the cardiac myosin, for example and with preferenceomecamtiv mecarbil (CK-1827452);

calcium-sensitizers, for example and with preference levosimendan;

agents that affect the energy metabolism of the heart, for example andwith preference etomoxir, dichloroacetat, ranolazine or trimetazidine,full or partial adenosine A1 receptor agonists such as GS-9667 (formerlyknown as CVT-3619), capadenoson, neladenoson and BAY 1067197;

agents that affect the heart rate, for example and with preferenceivabradin;

Antithrombotic agents are preferably understood to mean compounds fromthe group of the platelet aggregation inhibitors, the anticoagulants orthe profibrinolytic substances.

In a preferred embodiment of the invention, the inventive compounds areadministered in combination with a platelet aggregation inhibitor, byway of example and with preference aspirin, clopidogrel, prasugrel,ticagrelor, ticlopidin or dipyridamole.

In a preferred embodiment of the invention, the inventive compounds areadministered in combination with a thrombin inhibitor, by way of exampleand with preference ximelagatran, dabigatran, melagatran, bivalirudin orclexane.

In a preferred embodiment of the invention, the inventive compounds areadministered in combination with a GPIIb/IIIa antagonist such as, by wayof example and with preference, tirofiban or abciximab.

In a preferred embodiment of the invention, the inventive compounds areadministered in combination with a factor Xa inhibitor, by way ofexample and with preference rivaroxaban (BAY 59-7939), DU-176b,apixaban, betrixaban, otamixaban, fidexaban, razaxaban, letaxaban,eribaxaban, fondaparinux, idraparinux, PMD -3112, dare xaban (YM-150),KFA-1982, EMD-503982, MCM-17, MLN-1021, DX 9065a, DPC 906, JTV 803,SSR-126512 or SSR-128428.

In a preferred embodiment of the invention, the inventive compounds areadministered in combination with heparin or with a low molecular weight(LMW) heparin derivative.

In a preferred embodiment of the invention, the inventive compounds areadministered in combination with a vitamin K antagonist, by way ofexample and with preference coumarin.

Hypotensive agents are preferably understood to mean compounds from thegroup of the calcium antagonists, angiotensin All antagonists, ACEinhibitors, endothelin antagonists, renin inhibitors, alpha-receptorblockers, beta-receptor blockers, mineralocorticoid receptorantagonists, rho-kinase inhibitors and the diuretics.

In a preferred embodiment of the invention, the inventive compounds areadministered in combination with a calcium antagonist, by way of exampleand with preference nifedipine, amlodipine, verapamil or diltiazem.

In a preferred embodiment of the invention, the inventive compounds areadministered in combination with an alpha-1-receptor blocker, by way ofexample and with preference prazosin.

In a preferred embodiment of the invention, the inventive compounds areadministered in combination with a beta-receptor blocker, by way ofexample and with preference propranolol, atenolol, timolol, pindolol,alprenolol, oxprenolol, penbutolol, bupranolol, metipranolol, nadolol,mepindolol, carazalol, sotalol, metoprolol, betaxolol, celiprolol,bisoprolol, carteolol, esmolol, labetalol, carvedilol, adaprolol,landiolol, nebivolol, epanolol or bucindolol.

In a preferred embodiment of the invention, the inventive compounds areadministered in combination with an angiotensin AII antagonist, by wayof example and with preference losartan, candesartan, valsartan,telmisartan or embusartan or a dual angiotensin AII antagonist/neprilysin-inhibitor, by way of example and with preference LCZ696(valsartan/sacubitril).

In a preferred embodiment of the invention, the inventive compounds areadministered in combination with an ACE inhibitor, by way of example andwith preference enalapril, captopril, lisinopril, ramipril, delapril,fosinopril, quinopril, perindopril or trandopril.

In a preferred embodiment of the invention, the inventive compounds areadministered in combination with an endothelin antagonist, by way ofexample and with preference bosentan, darusentan, ambrisentan orsitaxsentan.

In a preferred embodiment of the invention, the inventive compounds areadministered in combination with a renin inhibitor, by way of exampleand with preference aliskiren, SPP-600 or SPP-800.

In a preferred embodiment of the invention, the inventive compounds areadministered in combination with a mineralocorticoid receptorantagonist, by way of example and with preference spironolactone oreplerenone.

In a preferred embodiment of the invention, the inventive compounds areadministered in combination with a loop diuretic, for examplefurosemide, torasemide, bumetanide and piretanide, withpotassium-sparing diuretics, for example amiloride and triamterene, withaldosterone antagonists, for example spironolactone, potassiumcanrenoate and eplerenone, and also thiazide diuretics, for examplehydrochlorothiazide, chlorthalidone, xipamide and indapamide.

Lipid metabolism modifiers are preferably understood to mean compoundsfrom the group of the CETP inhibitors, thyroid receptor agonists,cholesterol synthesis inhibitors such as HMG-CoA reductase inhibitors orsqualene synthesis inhibitors, the ACAT inhibitors, MTP inhibitors,PPAR-alpha, PPAR-gamma and/or PPAR-delta agonists, cholesterolabsorption inhibitors, polymeric bile acid adsorbents, bile acidreabsorption inhibitors, lipase inhibitors and the lipoprotein(a)antagonists.

In a preferred embodiment of the invention, the inventive compounds areadministered in combination with a CETP inhibitor, by way of example andwith preference dalcetrapib,anacetrapib, torcetrapib (CP-529 414),JJT-705 or CETP vaccine (Avant).

In a preferred embodiment of the invention, the inventive compounds areadministered in combination with a thyroid receptor agonist, by way ofexample and with preference D-thyroxine, 3,5,3′-triiodothyronine (T3),CGS 23425 or axitirome (CGS 26214).

In a preferred embodiment of the invention, the inventive compounds areadministered in combination with an HMG-CoA reductase inhibitor from theclass of statins, by way of example and with preference lovastatin,simvastatin, pravastatin, fluvastatin, atorvastatin, rosuvastatin orpitavastatin.

In a preferred embodiment of the invention, the inventive compounds areadministered in combination with a squalene synthesis inhibitor, by wayof example and with preference BMS-188494 or TAK-475.

In a preferred embodiment of the invention, the inventive compounds areadministered in combination with an ACAT inhibitor, by way of exampleand with preference avasimibe, melinamide, pactimibe, eflucimibe orSMP-797.

In a preferred embodiment of the invention, the inventive compounds areadministered in combination with an MTP inhibitor, by way of example andwith preference implitapide, BMS-201038, R-103757 or JTT-130.

In a preferred embodiment of the invention, the inventive compounds areadministered in combination with a PPAR-gamma agonist, by way of exampleand with preference pioglitazone or rosiglitazone.

In a preferred embodiment of the invention, the inventive compounds areadministered in combination with a PPAR-delta agonist, by way of exampleand with preference GW 501516 or BAY 68-5042.

In a preferred embodiment of the invention, the inventive compounds areadministered in combination with a cholesterol absorption inhibitor, byway of example and with preference ezetimibe, tiqueside or pamaque side.

In a preferred embodiment of the invention, the inventive compounds areadministered in combination with a lipase inhibitor, a preferred examplebeing orlistat.

In a preferred embodiment of the invention, the inventive compounds areadministered in combination with a polymeric bile acid adsorbent, by wayof example and with preference cholestyramine, colestipol, colesolvam,CholestaGel or colestimide.

In a preferred embodiment of the invention, the inventive compounds areadministered in combination with a bile acid reabsorption inhibitor, byway of example and with preference ASBT (=IBAT) inhibitors, for exampleAZD-7806, S-8921, AK-105, BARI-1741, SC-435 or SC-635.

In a preferred embodiment of the invention, the inventive compounds areadministered in combination with a lipoprotein(a) antagonist, by way ofexample and with preference, gemcabene calcium (CI-1027) or nicotinicacid.

In a preferred embodiment of the invention, the inventive compounds areadministered in combination with a lipoprotein(a) antagonist, by way ofexample and with preference, gemcabene calcium (CI-1027) or nicotinicacid.

In a preferred embodiment of the invention, the inventive compounds areadministered in combination with sGC modulators, by way of example andwith preference, riociguat, cinaciguat or vericiguat.

In a preferred embodiment of the invention, the inventive compounds areadministered in combination with an agent affecting the glucosemetabolism, by way of example and with preference, insuline, a sulfonylurea, acarbose, DPP4 inhibitors, GLP-1 analogs or SGLT-1 inhibitors.

In a preferred embodiment of the invention, the compounds according tothe invention are administered in combination with a TGFbeta antagonist,by way of example and with preference pirfenidone or fresolimumab.

In a preferred embodiment of the invention, the compounds according tothe invention are administered in combination with a CCR2 antagonist, byway of example and with preference CCX-140.

In a preferred embodiment of the invention, the compounds according tothe invention are administered in combination with a TNFalphaantagonist, by way of example and with preference adalimumab.

In a preferred embodiment of the invention, the compounds according tothe invention are administered in combination with a galectin-3inhibitor, by way of example and with preference GCS-100.

In a preferred embodiment of the invention, the compounds according tothe invention are administered in combination with a Nrf-2 inhibitor, byway of example and with preference bardoxolone

In a preferred embodiment of the invention, the compounds according tothe invention are administered in combination with a BMP-7 agonist, byway of example and with preference THR-184.

In a preferred embodiment of the invention, the compounds according tothe invention are administered in combination with a NOX1/4 inhibitor,by way of example and with preference GKT-137831.

In a preferred embodiment of the invention, the compounds according tothe invention are administered in combination with a medicament whichaffects the vitamin D metabolism, by way of example and with preferencecalcitriol, alfacalcidol, doxercalciferol, maxacalcitol, paricalcitol,cholecalciferol or paracalcitol.

In a preferred embodiment of the invention, the compounds according tothe invention are administered in combination with a cytostatic agent,by way of example and with preference cyclophosphamide.

In a preferred embodiment of the invention, the compounds according tothe invention are administered in combination with an immunosuppressiveagent, by way of example and with preference ciclosporin.

In a preferred embodiment of the invention, the compounds according tothe invention are administered in combination with a phosphate binder,by way of example and with preference colestilan, sevelamerhydrochloride and sevelamer carbonate, Lanthanum and lanthanumcarbonate.

In a preferred embodiment of the invention, the compounds according tothe invention are administered in combination with renal proximal tubulesodium-phosphate co-transporter, by way of example and with preference,niacin or nicotinamide.

In a preferred embodiment of the invention, the compounds according tothe invention are administered in combination with a calcimimetic fortherapy of hyperparathyroidism.

In a preferred embodiment of the invention, the compounds according tothe invention are administered in combination with agents for irondeficit therapy, by way of example and with preference iron products.

In a preferred embodiment of the invention, the compounds according tothe invention are administered in combination with agents for thetherapy of hyperurikaemia, by way of example and with preferenceallopurinol or rasburicase.

In a preferred embodiment of the invention, the compounds according tothe invention are administered in combination with glycoprotein hormonefor the therapy of anaemia, by way of example and with preferenceerythropoietin.

In a preferred embodiment of the invention, the compounds according tothe invention are administered in combination with biologics for immunetherapy, by way of example and with preference abatacept, rituximab,eculizumab or belimumab.

In a preferred embodiment of the invention, the compounds according tothe invention are administered in combination with vasopressinantagonists (group of the vaptanes) for the treatment of heart failure,by way of example and with preference tolvaptan, conivaptan, lixivaptan,mozavaptan, satavaptan or relcovaptan.

In a preferred embodiment of the invention, the compounds according tothe invention are administered in combination with Jak inhibitors, byway of example and with preference ruxolitinib, tofacitinib,baricitinib, CYT387, GSK2586184, lestaurtinib, pacritinib (SB1518) orTG101348.

In a preferred embodiment of the invention, the compounds according tothe invention are administered in combination with prostacyclin analogsfor therapy of microthrombi.

In a preferred embodiment of the invention, the compounds according tothe invention are administered in combination with an alkali therapy, byway of example and with preference sodium bicarbonate.

In a preferred embodiment of the invention, the compounds according tothe invention are administered in combination with an mTOR inhibitor, byway of example and with preference everolimus or rapamycin.

In a preferred embodiment of the invention, the compounds according tothe invention are administered in combination with an NHE3 inhibitor, byway of example and with preference AZD1722 or tenapanor.

In a preferred embodiment of the invention, the compounds according tothe invention are administered in combination with an eNOS modulator, byway of example and with preference sapropterin.

In a preferred embodiment of the invention, the compounds according tothe invention are administered in combination with a CTGF inhibitor, byway of example and with preference FG-3019.

In a particular preferred embodiment of the invention, the inventivecompounds are administered in combination with one or more furtheragents selected from the group of the hypotensive active compounds, ofthe antiinflammatory agents/immunosuppressive agents, the phosphatebinders, the sodium-phosphate co-transporters, NHE3 inhibitors,antiarrhythmic agents, agents that alter lipid metabolism and/or theactive compounds which modulate vitamin D metabolism.

Based upon standard laboratory techniques known to evaluate compoundsuseful for the treatment of diseases and/or conditions associated withhyperphosphatemia, chronic kidney disease (CKD), chronic kidney diseaseassociated calcification, non-chronic kidney disease associatedcalcification, media calcifications including Moenckeberg's medialsclerosis, atherosclerosis, intima calcification, CKD associated hearthypertrophy, CKD associated renal dystrophy, osteoporosis,post-menopausal osteoporosis, diabetes mellitus II, chronic renaldisease, aging, hypophosphaturia, hyperparathyroidism, Vitamin Ddisorders, Vitamin K deficiency, Vitamin K-antagonist coagulants,Kawasaki disease, ACDC (arterial calcification due to deficiency ofCD73), GACI (generalized arterial calcification of infancy), IBGC(idiopathic basal ganglia calcification), PXE (pseudoxanthomaelasticum), rheumatoid arthritis, Singleton-Merten syndrome,P-thalassemia,calciphylaxis, heterotrophic ossification, pretermplacental calcification, calcification of the uterus, calcified uterinefibroids, morbus fahr, mircocalcification and calcification of theaortic valve, by standard toxicity tests and by standard pharmacologicalassays for the determination of treatment of the conditions identifiedabove in mammals, and by comparison of these results with the results ofknown active ingredients or medicaments that are used to treat theseconditions, the effective dosage of the compounds of the presentinvention can readily be determined for treatment of each desiredindication. The amount of the active ingredient to be administered inthe treatment of one of these conditions can vary widely according tosuch considerations as the particular compound and dosage unit employed,the mode of administration, the period of treatment, the age and sex ofthe patient treated, and the nature and extent of the condition treated.

The total amount of the active ingredient to be administered willgenerally range from about 0.001 mg/kg to about 200 mg/kg body weightper day, and preferably from about 0.01 mg/kg to about 50 mg/kg bodyweight per day, and more preferably from about 0.01 mg/kg to about 20mg/kg body weight per day. Clinically useful dosing schedules will rangefrom one to three times a day dosing to once every four weeks dosing. Inaddition, it is possible for “drug holidays”, in which a patient is notdosed with a drug for a certain period of time, to be beneficial to theoverall balance between pharmacological effect and tolerability. It ispossible for a unit dosage to contain from about 0.5 mg to about 1500 mgof active ingredient, and can be administered one or more times per dayor less than once a day. The average daily dosage for administration byinjection, including intravenous, intramuscular, subcutaneous andparenteral injections, and use of infusion techniques will preferably befrom 0.01 to 200 mg/kg of total body weight. The average daily rectaldosage regimen will preferably be from 0.01 to 200 mg/kg of total bodyweight. The average daily vaginal dosage regimen will preferably be from0.01 to 200 mg/kg of total body weight. The average daily topical dosageregimen will preferably be from 0.1 to 200 mg administered between oneto four times daily. The transdermal concentration will preferably bethat required to maintain a daily dose of from 0.01 to 200 mg/kg. Theaverage daily inhalation dosage regimen will preferably be from 0.01 to100 mg/kg of total body weight. The average daily oral dosage regimenwill preferably be from 0.01 to 30 mg/kg of total body weight.

Of course the specific initial and continuing dosage regimen for eachpatient will vary according to the nature and severity of the conditionas determined by the attending diagnostician, the activity of thespecific compound employed, the age and general condition of thepatient, time of administration, route of administration, rate ofexcretion of the drug, drug combinations, and the like. The desired modeof treatment and number of doses of a compound of the present inventionor a pharmaceutically acceptable salt or ester or composition thereofcan be ascertained by those skilled in the art using conventionaltreatment tests.

Nevertheless, it may optionally be necessary to deviate from the statedamounts, namely depending on body weight, route of administration,individual response to the active substance, type of preparation andtime point or interval when application takes place. Thus, in some casesit may be sufficient to use less than the aforementioned minimum amount,whereas in other cases the stated upper limit must be exceeded. Whenapplying larger amounts, it may be advisable to distribute these inseveral individual doses throughout the day.

According to a further embodiment, the compounds of formula (I)according to the invention are administered orally once or twice orthree times a day. According to a further embodiment, the compounds offormula (I) according to the invention are administered orally once ortwice a day. According to a further embodiment, the compounds of formula(I) according to the invention are administered orally once a day. Forthe oral administration, a rapid release or a modified release dosageform may be used.

EXPERIMENTAL SECTION

The following table 1 lists the abbreviations used in this paragraph andin the Examples section as far as they are not explained within the textbody. Other abbreviations have their meanings customary per se to theskilled person.

TABLE 1 Abbreviations Abbreviation Meaning DBU1,8-diazabicycloundec-7-ene dichloromethane dichloromethane DMSOdimethyl sulfoxide EDTA ethylenediaminetetraacetic acid MTBE methyltert-butyl ether NMR nuclear magnetic resonance NMPN-Methyl-2-pyrrolidone DMF N,N-dimethylformamide MS mass spectroscopyR_(t) retention time HPLC, LC high performance liquid chromatography hhour min minute ppm chemical shift δ in parts per million s singlet ddoublet dd doublet of doublet m multiplet ESI electrospray ionisationphosphazen- 1-Ethyl-2,2,4,4,4-pentakis(dimethylamino)- base P(2)-Et2λ5,4λ5-catenadi(phosphazene) pos positive neg negative DAD Diode ArrayDetector m/z mass-to-charge ratio (in mass spectrum) TFA trifluoroaceticacid THF tetrahydrofuran tBuBrettPhos Pd[(2-Di-tert-butylphosphino-3,6-dimethoxy-2′,4′,6′- G3triisopropyl-1,1′-biphenyl)-2-(2′-amino-1,1′- biphenyl)]palladium(II)methanesulfonate SFC supercritical fluid chromatography XantPhos4,5-Bis(diphenylphosphino)-9,9-dimethylxanthene

Other abbreviations not specified herein have their meanings customaryto the skilled person.

The various aspects of the invention described in this application areillustrated by the following examples which are not meant to limit theinvention in any way.

The example testing experiments described herein serve to illustrate thepresent invention and the invention is not limited to the examplesgiven.

EXPERIMENTAL SECTION—GENERAL PART

All reagents, for which the synthesis is not described in theexperimental part, are either commercially available, or are knowncompounds or may be formed from known compounds by known methods by aperson skilled in the art.

The compounds and intermediates produced according to the methods of theinvention may require purification. Purification of organic compounds iswell known to the person skilled in the art and there may be severalways of purifying the same compound. In some cases, no purification maybe necessary. In some cases, the compounds may be purified bycrystallization. In some cases, impurities may be stirred out using asuitable solvent. In some cases, the compounds may be purified bychromatography, particularly flash column chromatography, using forexample prepacked silica gel cartridges, e.g. Biotage SNAP cartidgesKP-Sil® or KP-NH® in combination with a Biotage autopurifier system(SP4® or Isolera Four®) and eluents such as gradients of hexane/ethylacetate or DCM/methanol. In some cases, the compounds may be purified bypreparative HPLC using for example a Waters autopurifier equipped with adiode array detector and/or on-line electrospray ionization massspectrometer in combination with a suitable prepacked reverse phasecolumn and eluents such as gradients of water and acetonitrile which maycontain additives such as trifluoroacetic acid, formic acid or aqueousammonia.

In some cases, purification methods as described above can provide thosecompounds of the present invention which possess a sufficiently basic oracidic functionality in the form of a salt, such as, in the case of acompound of the present invention which is sufficiently basic, atrifluoroacetate or formate salt for example, or, in the case of acompound of the present invention which is sufficiently acidic, anammonium salt for example. A salt of this type can either be transformedinto its free base or free acid form, respectively, by various methodsknown to the person skilled in the art, or be used as salts insubsequent biological assays. It is to be understood that the specificform (e.g. salt, free base etc.) of a compound of the present inventionas isolated and as described herein is not necessarily the only form inwhich said compound can be applied to a biological assay in order toquantify the specific biological activity.

NMR peak forms are stated as they appear in the spectra, possible higherorder effects have not been considered.

The ¹H-NMR data of selected compounds are listed in the form of ¹H-NMRpeaklists. For each signal peak the δ value in ppm is given, followed bythe signal intensity, reported in round brackets. The δ value-signalintensity pairs from different peaks are separated by commas. Therefore,a peaklist is described by the general form: δ₁ (intensity₁), δ₂(intensity₂), . . . , δ_(i) (intensity_(i)), . . . , δ_(n)(intensity_(n)).

The intensity of a sharp signal correlates with the height (in cm) ofthe signal in a printed NMR spectrum. When compared with other signals,this data can be correlated to the real ratios of the signalintensities. In the case of broad signals, more than one peak, or thecenter of the signal along with their relative intensity, compared tothe most intense signal displayed in the spectrum, are shown. A ¹H-NMRpeaklist is similar to a classical ¹H-NMR readout, and thus usuallycontains all the peaks listed in a classical NMR interpretation.Moreover, similar to classical ¹H-NMR printouts, peaklists can showsolvent signals, signals derived from stereoisomers of target compounds(also the subject of the invention), and/or peaks of impurities. Thepeaks of stereoisomers, and/or peaks of impurities are typicallydisplayed with a lower intensity compared to the peaks of the targetcompounds (e.g., with a purity of >90%). Such stereoisomers and/orimpurities may be typical for the particular manufacturing process, andtherefore their peaks may help to identify the reproduction of ourmanufacturing process on the basis of “by-product fingerprints”. Anexpert who calculates the peaks of the target compounds by known methods(MestReC, ACD simulation, or by use of empirically evaluated expectationvalues), can isolate the peaks of target compounds as required,optionally using additional intensity filters. Such an operation wouldbe similar to peak-picking in classical ¹H-NMR interpretation. Adetailed description of the reporting of NMR data in the form ofpeaklists can be found in the publication “Citation of NMR Peaklist Datawithin Patent Applications” (cf. Research Disclosure Database Number605005, 2014, 1 Aug. 2014, orhttp://www.researchdisclosure.com/searching-disclosures). In the peakpicking routine, as described in the Research Disclosure Database Number605005, the parameter “MinimumHeight” can be adjusted between 1% and 4%.Depending on the chemical structure and/or depending on theconcentration of the measured compound it may be reasonable to set theparameter “MinimumHeight”<1%.

Chemical names were generated using the ACD/Name software from ACD/Labs.In some cases generally accepted names of commercially availablereagents were used in place of ACD/Name generated names.

Reactions employing microwave irradiation may be run with a BiotageInitator® microwave oven optionally equipped with a robotic unit. Thereported reaction times employing microwave heating are intended to beunderstood as fixed reaction times after reaching the indicated reactiontemperature. The compounds and intermediates produced according to themethods of the invention may require purification. Purification oforganic compounds is well known to the person skilled in the art andthere may be several ways of purifying the same compound. In some cases,no purification may be necessary. In some cases, the compounds may bepurified by crystallization. In some cases, impurities may be stirredout using a suitable solvent. In some cases, the compounds may bepurified by chromatography, particularly flash column chromatography,using for example prepacked silica gel cartridges, e.g. from Separtissuch as Isolute® Flash silica gel or Isolute® Flash NH2 silica gel incombination with a Isolera autopurifier (Biotage) and eluents such asgradients of e.g. hexane/EE or dichloromethane/methanol. In some cases,the compounds may be purified by preparative HPLC using for example aWaters autopurifier equipped with a diode array detector and/or on-lineelectrospray ionization mass spectrometer in combination with a suitableprepacked reverse phase column and eluents such as gradients of waterand acetonitrile which may contain additives such as trifluoroaceticacid, formic acid or aqueous ammonia. In some cases, purificationmethods as described above can provide those compounds of the presentinvention which possess a sufficiently basic or acidic functionality inthe form of a salt, such as, in the case of a compound of the presentinvention which is sufficiently basic, a trifluoroacetate or formatesalt for example, or, in the case of a compound of the present inventionwhich is sufficiently acidic, an ammonium salt for example. A salt ofthis type can either be transformed into its free base or free acidform, respectively, by various methods known to the person skilled inthe art, or be used as salts in subsequent biological assays. It is tobe understood that the specific form (e.g. salt, free base etc) of acompound of the present invention as isolated as described herein is notnecessarily the only form in which said compound can be applied to abiological assay in order to quantify the specific biological activity.

The percentage yields reported in the following examples are based onthe starting component that was used in the lowest molar amount. Air andmoisture sensitive liquids and solutions were transferred via syringe orcannula, and introduced into reaction vessels through rubber septa.Commercial grade reagents and solvents were used without furtherpurification. The term “concentrated in vacuum” refers to use of a Buchirotary evaporator at a minimum pressure of approximately 15 mm of Hg.All temperatures are reported uncorrected in degrees Celsius (° C.).

In order that this invention may be better understood, the followingexamples are set forth. These examples are for the purpose ofillustration only, and are not to be construed as limiting the scope ofthe invention in any manner All publications mentioned herein areincorporated by reference in their entirety.

Methods

Preparative HPLC

Methods for purifications by preparative HPLC given in the subsequentspecific experimental descriptions refer (unless otherwise noted) to thefollowing conditions:

Method 1: Instrument: Waters Prep LC/MS System, Column: XBridge C18 5 μm100×30 mm; Eluent A: water, eluent B: acetonitrile, eluent C: 2% aqueousammonia solution, eluent D: acetonitrile/water 80/20. flow: 80 ml/min,room temperature, detection wavelength 200-400 nm, At-column injection;gradient: 0-2 min 59% eluent A, 29% eluent B, 2-10 min 59 to 29% eluentA, 29 to 59% eluent B, 10-12 min 0% eluent A, 88% eluent B, eluent C andD constantly 6% each over the whole run-time.

Method 2: Instrument: Waters Prep LC/MS System, Column: XBridge C18 5 μm100×30 mm; Eluent A: water, eluent B: acetonitrile, eluent C: 2% aqueousformic acid solution, eluent D: acetonitrile/water 80/20. flow: 80ml/min, room temperature, detection wavelength 200-400 nm, At-columninjection; gradient: 0-2 min 59% eluent A, 29% eluent B, 2-10 min 59 to29% eluent A, 29 to 59% eluent B, 10-12 min 0% eluent A, 88% eluent B,eluent C and D constantly 6% each over the whole run-time.

Method 3: Instrument: Waters Prep LC/MS System, column: PhenomenexKinetex C18 5 μm 100×30 mm; eluent A: water, eluent B: acetonitrile,eluent C: 2% aqueous formic acid in water, eluent D: acetonitrile/water80/20. flow: 80 ml/min, room temperature, detection wavelength 200-400nm, At-Column injection; gradient: 0-2 min 59% eluent A, 29% eluent B,2-10 min 59 to 29% eluent A, 29 to 59% eluent B, 10-12 min 0% eluent A,88% eluent B, eluent C and D constantly 6% each over the whole run-time.

Method 4: Instrument: Waters Prep LC/MS System, column: PhenomenexKinetex C18 5 μm 100×30 mm; eluent A: water, eluent B: acetonitrile,eluent C: 2% aqueous formic acid in water, eluent D: acetonitrile/water80/20. flow: 80 ml/min, room temperature, detection wavelength 200-400nm, At-Column injection; gradient: 0-2 min 49% eluent A, 39% eluent B,2-10 min 49 to 19% eluent A, 39 to 69% eluent B, 10-12 min 0% eluent A,88% eluent B, eluent C and D constantly 6% each over the whole run-time.

Method 5: Instrument: Waters Prep LC/MS System, column: PhenomenexKinetex C18 5 μm 100×30 mm; eluent A: water, eluent B: acetonitrile,eluent C: 2% aqueous formic acid in water, eluent D: acetonitrile/water80/20. flow: 80 ml/min, room temperature, detection wavelength 200-400nm, At-Column injection; gradient: 0-2 min 29% eluent A, 59% eluent B,2-10 min 29 to 0% eluent A, 59 to 88% eluent B, 10-12 min 0% eluent A,88% eluent B, eluent C and D constantly 6% each over the whole run-time.

Method 6: Instrument: Waters Prep LC/MS System, Column: XBridge C18 5 μm100×30 mm; Eluent A: water, eluent B: acetonitrile, eluent C: 2% aqueousammonia solution, eluent D: acetonitrile/water 80/20. flow: 80 ml/min,room temperature, detection wavelength 200-400 nm, At-column injection;gradient: 0-2 min 49% eluent A, 39% eluent B, 2-10 min 49 to 39% eluentA, 39 to 49% eluent B, 10-12 min 0% eluent A, 88% eluent B, eluent C andD constantly 6% each over the whole run-time.

Method 7: Instrument: Waters Prep LC/MS System, column: PhenomenexKinetex C18 5 μm 100×30 mm; eluent A: water, eluent B: acetonitrile,eluent C: 2% aqueous formic acid in water, eluent D: acetonitrile/water80/20. flow: 80 ml/min, room temperature, detection wavelength 200-400nm, At-Column injection; gradient: 0-2 min 69% eluent A, 19% eluent B,2-10 min 69 to 39% eluent A, 19 to 49% eluent B, 10-12 min 0% eluent A,88% eluent B, eluent C and D constantly 6% each over the whole run-time.

Method 8: Instrument: Waters Prep LC/MS System, Column: XBridge C18 5 μm100×30 mm; Eluent A: water, eluent B: acetonitrile, eluent C: 2% aqueousammonia solution, eluent D: acetonitrile/water 80/20. flow: 80 ml/min,room temperature, detection wavelength 200-400 nm, At-column injection;gradient: 0-2 min 29% eluent A, 59% eluent B, 2-10 min 29 to 0% eluentA, 59 to 88% eluent B, 10-12 min 0% eluent A, 88% eluent B, eluent C andD constantly 6% each over the whole nm-time.

Method 17: Instrument: Waters Prep LC/MS System, Column: XBridge C18 5μm 100×30 mm; Eluent A: water, eluent B: acetonitrile, eluent C: 2%aqueous ammonia solution, eluent D: acetonitrile/water 80/20. flow: 80ml/min, room temperature, detection wavelength 200-400 nm, At-columninjection; gradient: 0-2 min 69% eluent A, 19% eluent B, 2-10 min 69 to19% eluent A, 19 to 69% eluent B, 10-12 min 0% eluent A, 88% eluent B,eluent C and D constantly 6% each over the whole run-time.

Method 18: Instrument: Waters Prep LC/MS System, Column: XBridge C18 5μm 100×30 mm; Eluent A: water, eluent B: acetonitrile, eluent C: 2%aqueous ammonia solution, eluent D: acetonitrile/water 80/20. flow: 80ml/min, room temperature, detection wavelength 200-400 nm, At-columninjection; gradient: 0-2 min 79% eluent A, 9% eluent B, 2-10 min 79 to49% eluent A, 9 to 39% eluent B, 10-12 min 0% eluent A, 88% eluent B,eluent C and D constantly 6% each over the whole run-time.

Method 19: Instrument: Knauer Azura, column: Chromatorex C18 10 μm, 125mm×40 mm; eluent A: water, eluent B: acetonitrile; flow: 100 ml/min;room temperature, wavelength 210 nm, gradient: 0-3 min 20% eluent B,3-21 min 20% eluent B to 95% eluent B, 21-24 min 95% eluent B, 24-25 min95% eluent B to 20% eluent B, 25-27.5 min 20% eluent B.

Method 20: Instrument: Waters Prep LC/MS System, column: DaicelChiralpak IF 5 μm, 250 mm×20 mm; eluent: ethanol; flow: 15 ml/min;temperature 70 C, wavelength 220 nm; gradient: 0-15 min 100% ethanol.

Analytical HPLC/LC/MS

LC-MS-data given in the subsequent specific experimental descriptionsrefer (unless otherwise noted) to the following conditions:

Method 9: Instrument: Waters ACQUITY SQD UPLC System; Column: WatersAcquity UPLC HSS T3 1.8μ 50×1 mm; eluent A: 1 l water+0.25 ml 99% igeformic acid, eluent B: 1 l acetonitrile+0.25 ml 99% formic acid;gradient: 0.0 min 90% A→1.2 min 5% A→2.0 min 5% A temperature: 50° C.;flow: 0.40 ml/min; UV-detection: 208-400 nm.

Method 10: Instrument: Thermo Scientific FT-MS; Instrument UHPLC+:Thermo Scientific UltiMate 3000; column: Waters, HSST3, 2.1×75 mm, C181.8 μm; eluent A: 11 water+0.01% formic acid; eluent B: 1 lacetonitrile+0.01% formic acid; gradient: 0.0 min 10% B→2.5 min 95%B→3.5 min 95% B; temperature: 50° C.; flow: 0.90 ml/min; UV-detection:210 nm/optimal Integration Path 210-300 nm.

Method 11: Instrument: Agilent MS Quad 6150;HPLC: Agilent 1290; column:Waters Acquity UPLC HSS T3 1.8μ 50×2.1 mm; eluent A: 1 l water+0.25 ml99% formic acid, eluent B: 1 l acetonitrile+0.25 ml 99% ige formic acid;gradient: 0.0 min 90% A→0.3 min 90% A→1.7 min 5% A→3.0 min 5% Atemperature: 50° C.; flow: 1,20 ml/min; UV-detection: 205-305 nm.

Method 12: Instrument MS: ThermoFisherScientific LTQ-Orbitrap-XL; typeHPLC: Agilent 1200SL; column: Agilent, POROSHELL 120, 3×150 mm, SB—C182.7 μm; eluent A: 1 l water+0.1% TFA; eluent B: 1 l acetonitrile+0.1%TFA; gradient: 0.0 min 2% B→0.3 min 2% B→5.0 min 95% B→10.0 min 95% B;temperature: 40° C.; flow: 0.75 ml/min; UV-detection: 210 nm.

Method 13: Instrument: Waters Acquity UPLCMS SingleQuad; column: AcquityUPLC BEH C18 1.7 μm, 50×2.1 mm; eluent A: water+0.1 Vol-% TFA (99%),eluent B: acetonitrile; gradient: 0-1.6 min 1-99% B, 1.6-2.0 min 99% B;flow 0.8 ml/min; temperature: 60° C.; DAD scan: 210-400 nm.

Method 14: Instrument: Waters ACQUITY SQD UPLC System; column: WatersAcquity UPLC HSS T3 1.8μ 50×1 mm; eluent A: 1 1 water+0.25 ml formicacid (99%), eluent B: 1 l acetonitrile+0.25 ml formic acid (99%);gradient: 0.0 min 95% A→6.0 min 5% A→7.5 min 5% A temperature: 50° C.;flow: 0.35 ml/min; UV-detection: 210-400 nm.

Method 16: Instrument: Waters Single Quad MS System; Instrument WatersUPLC Acquity; Säule: Waters BEH C18 1.7μ 50×2.1 mm; Eluent A: 1 lWasser+1.0 mL (25% ig Ammoniak)/L, Eluent B: 1 l Acetonitril; Gradient:0.0 min 92% A→0.1 min 92% A→1.8 min 5% A→3.5 min 5% A; Ofen: 50° C.;Fluss: 0.45 mL/min; UV-Detektion: 210 nm (208-400 nm).

Method 21: Instrument: Waters Single Quad MS System; Instrument WatersUPLC Acquity; column: Waters BEH C18 1.7 μm 50×2.1 mm; Eluent A: 1 lWafter+1.0 mL (25% ammonia)/L, Eluent B: 1 l acetonitrile; gradient: 0.0min 92% A→0.1 min 92% A→1.8 min 5% A→3.5 min 5% A; temperature: 50° C.;flow: 0.45 mL/min; UV-detection: 210 nm (208-400 nm).

GC-MS

GC-MS-data given in the subsequent specific experimental descriptionsrefer (unless otherwise noted) to the following conditions:

Method 15: Instrument: Thermo Scientific DSQII, Thermo Scientific TraceGC Ultra; column: Restek RTX-35MS, 15 m×200 μm×0.33 μm; constant flowwith helium: 1.20 ml/min; temperature: 60° C.; Inlet: 220° C.; gradient:60° C., 30° C./min→300° C. (3.33 min hold).

Synthetic Intermediates Intermediate 14-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine

A solution of 4,6-dichloropyrimidine (10.0 g, 67.1 mmol) and3,5-dimethyl-1H-pyrazole (6.45 g, 67.1 mmol) in DMF (42 mL) was treatedwith caesium carbonate (21.9 g, 67.1 mmol). The resulting mixture wasstirred overnight at room temperature. The mixture was poured into 700mL water, the resulting precipitate was collected by filtration, washedwith water and dried to yield 4.8 g (34% yield) of the desired compound.

LC-MS (method 9): Rt=0.97 min; MS (ESIpos): m/z=209 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.016 (0.62), 2.218 (16.00), 2.654(13.00), 6.259 (2.71), 7.886 (2.77), 8.891 (2.48).

Intermediate 2 2-(4-fluorobenzoyl)butanenitrile

A solution of butyronitrile (3.8 mL, 43 mmol) in THF (100 mL) wastreated with lithium bis(trimethylsilyl)amide (1M in THF; 130 mL, 1.0 M,130 mmol) at 30° C. Afterwards ethyl 4-fluorobenzoate (19 ml, 130 mmol)was added dropwise. The resulting mixture was stirred for 1 hour. Thereaction was quenched by the addition of water and extracted once withMTBE. The aqueous phase was acidified with aqueous hydrochloric acid topH 2 and subsequently extracted three times with dichloromethane. Thecombined organic phases were washed over sodium sulphate and the solventwas removed under reduced pressure to yield the crude desired product(8.31 g, 79% yield) which was used in the next step without any furtherpurification.

LC-MS (method 9): R_(t)=0.87 min; MS (ESIneg): m/z=190 [M−H]⁻

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: 1.008 (7.45), 1.026 (16.00), 1.045(8.04), 1.069 (1.74), 1.088 (3.54), 1.106 (1.75), 1.164 (0.61), 1.182(1.20), 1.199 (0.61), 1.783 (0.97), 1.801 (1.56), 1.818 (1.97), 1.837(2.21), 1.855 (1.41), 1.920 (0.42), 1.939 (1.38), 1.952 (1.59), 1.957(1.80), 1.971 (1.79), 1.995 (2.77), 2.005 (0.87), 2.281 (0.58), 2.300(1.71), 2.318 (1.65), 2.337 (0.54), 3.346 (0.47), 4.028 (0.54), 4.046(0.53), 5.147 (2.40), 5.160 (2.72), 5.167 (2.73), 5.180 (2.35), 7.295(0.92), 7.299 (0.88), 7.317 (1.89), 7.339 (1.13), 7.410 (3.19), 7.433(6.51), 7.455 (3.58), 7.599 (1.03), 7.613 (1.18), 7.621 (1.07), 7.634(0.92), 7.998 (0.45), 8.013 (0.52), 8.020 (0.48), 8.034 (0.46), 8.109(4.31), 8.114 (2.38), 8.123 (4.89), 8.131 (4.74), 8.145 (4.13), 10.860(0.97).

Intermediate 3 4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-amine

A solution of 2-(4-fluorobenzoyl)butanenitrile (6.50 g, 34.0 mmol) inethanol (80 mL) was treated with hydrazine hydrate (1:1) (2.0 ml, 41mmol). The mixture was refluxed for 3 hours. After cooling to roomtemperature the mixture was poured into sodium hydrogen carbonatesolution (1M). Ethanol was removed under reduced pressure, the resultingprecipitate was collected by filtration, washed with water and dried toyield 5.68 g (81% yield) of the desired product.

LC-MS (method 9): R_(t)=0.62 min; MS (ESIpos): m/z=206 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 1.014 (7.35), 1.032 (16.00), 1.051(7.67), 2.388 (2.65), 2.407 (7.99), 2.425 (7.79), 2.444 (2.46), 3.327(5.49), 4.487 (1.85), 7.238 (2.73), 7.260 (5.64), 7.282 (3.26), 7.495(3.91), 7.509 (4.88), 7.515 (4.60), 7.529 (3.35), 11.519 (2.77).

Intermediate 4 ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

The desired product was obtained in the same manner as described for4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine starting from4,6-dichloropyrimidine (2.00 g, 13.4 mmol) and ethyl3,5-dimethyl-1H-pyrazole-4-carboxylate (2.26 g, 13.4 mmol) to yield 3.42g (90% yield) of the desired product.

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (0.47), 0.008 (0.43), 1.298(4.21), 1.316 (9.05), 1.325 (0.56), 1.334 (4.30), 2.415 (15.87), 2.441(0.55), 2.947 (16.00), 2.991 (0.53), 4.248 (1.31), 4.266 (4.11), 4.284(4.07), 4.301 (1.29), 7.994 (3.67), 7.996 (3.62), 9.013 (3.52), 9.015(3.52).

Intermediate 54-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine

A solution of 4-chloro-6-hydrazinylpyrimidine (1.00 g, 6.92 mmol,synthesis described e.g. Synlett 2010 (14), 2179-2183) and1,1-difluoropentane-2,4-dione (941 mg, 6.92 mmol) in ethanol (10 mL) wasrefluxed overnight. After cooling to room temperature, ethanol wasremoved under reduced pressure. The resulting crude product was purifiedby reverse phase HPLC (column: Daicel IC, 250×20 mm, flow 20 mL/min, 95%i-hexane/5% ethanol, room temperature, detection 220 nM) to yield 432 mg(25% yield) of the desired product.

LC-MS (method 11): R_(t)=1.35 min; MS (ESIpos): m/z=245 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.152 (0.03), 0.144 (0.03), 2.072(0.10), 2.170 (0.09), 2.332 (16.00), 2.365 (0.07), 2.669 (0.05), 2.709(0.04), 6.911 (3.24), 7.633 (1.27), 7.768 (2.50), 7.903 (1.23), 7.959(2.80), 8.961 (2.76).

Intermediate 66-chloro-N[4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]pyrimidin-4-amine

A solution of 4,6-dichloropyrimidine (2.18 g, 14.6 mmol) and4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-amine (3.00 g, 14.6 mmol) in DMF(33 mL) was treated with sodium iodide (2.63 g, 17.5 mmol) andN,N-diisopropylethylamine (2.8 mL, 16 mmol). The resulting mixture wasstirred overnight at 80° C. The amount of DMF was reduced under reducedpressure. The residue was diluted with ethyl acetate. The organic layerwas washed with water, brine and dried over sodium sulfate. The solventwas removed under reduced pressure, the remaining residue was trituratedwith diethyl ether to yield the crude product which was further purifiedby flash chromatography on silica gel (eluent: cyclohexane/ehyl acetate)to yield 1.54 g (33% yield) of the desired product.

LC-MS (method 10): R_(t)=1.68 min; MS (ESIpos): m/z=318 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.977 (6.99), 0.995 (16.00), 1.014(7.42), 1.912 (2.37), 7.060 (0.88), 7.330 (2.55), 7.352 (5.11), 7.374(2.89), 7.584 (3.62), 7.598 (4.37), 7.605 (3.97), 7.619 (2.95), 8.418(6.63), 9.682 (3.10), 12.802 (1.02).

Intermediate 7N-[4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]-6-hydrazinylpyrimidin-4-amine

A solution of6-chloro-N-[4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]pyrimidin-4-amine(500 mg, 1.57 mmol) in 1,4-dioxane (10 mL) was treated with hydrazinehydrate (1:1) (230 μl, 4.7 mmol). The resulting mixture was stirredovernight at 70° C. The solvent was removed under reduced pressure andthe remaining residue was suspended in acetonitrile. Crystals werecollected by filtration, washed with acetonitrile and dried to yield 509mg (99% yield) of the desired product.

LC-MS (method 10): R_(t)=0.97 min; MS (ESIpos): m/z=314 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.008 (0.43), 0.982 (7.51), 1.001(16.00), 1.019 (7.13), 2.075 (0.53), 2.479 (3.24), 4.157 (0.41), 6.255(0.51), 7.093 (1.10), 7.323 (3.07), 7.596 (3.51), 7.714 (0.89), 7.954(4.54), 12.623 (0.45).

Intermediate 82-[4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione

A solution of 4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-amine (1.00 g,4.87 mmol) and 2-benzofuran-1,3-dione (1.08 g, 7.31 mmol) in acetic acid(10 mL) was refluxed overnight. The mixture was poured into water andextracted with ethyl acetate. The combined organic phases were washedwith brine, dried over sodium sulfate and the solvent was removed underreduced pressure. The crude product was triturated with MTBE to afford1.37 g (84% yield) of the desired product.

LC-MS (method 9): R_(t)=0.97 min; MS (ESIpos): m/z=336 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.929 (7.10), 0.948 (16.00), 0.967(7.59), 1.994 (0.59), 2.419 (2.05), 2.437 (6.19), 2.456 (6.07), 2.475(1.97), 3.340 (3.09), 7.372 (3.70), 7.394 (7.88), 7.417 (4.38), 7.650(4.81), 7.664 (5.46), 7.672 (4.90), 7.685 (4.17), 7.953 (4.07), 7.961(4.99), 7.967 (5.39), 7.974 (7.34), 7.985 (1.68), 8.011 (1.41), 8.021(7.32), 8.029 (5.16), 8.035 (4.95), 8.042 (4.04), 13.386 (5.95).

Intermediate 92-[4-ethyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione

A solution of2-[4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(1.32 g, 3.94 mmol) in DMF (10 mL) was treated with potassium carbonate(1.09 g, 7.88 mmol) and iodomethane (490 μl, 7.9 mmol). The mixture wasstirred overnight at room temperature. The mixture was poured into waterand extracted with ethyl acetate. The combined organic phases werewashed with water, brine, dried over sodium sulfate and the solvent wasremoved under reduced pressure. The crude product was purified viapreparative HPLC (method: column: Reprosil C18; 10 μm; 125×30 mm/flow:50 ml/min/eluent: A=water (0.01% formic acid), B=acetonitrile/gradient:0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75 min=100% B, 19.75-23.00min=90% B) to yield 977.9 mg of the desired product as regioisomericmixture. After separation of the regioisomers via SFC using carbondioxide/methanol as eluents 312 mg of the desired product in a mixturewith the ring-opened phthalimide were obtained (13% yield).

LC-MS (method 10): R_(t)=2.03 min; MS (ESIpos): m/z=350 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.907 (3.03), 0.925 (6.88), 0.944(3.12), 1.050 (3.20), 1.069 (7.26), 1.088 (3.29), 2.438 (0.89), 2.457(2.66), 2.476 (2.65), 2.564 (2.73), 2.583 (2.64), 2.601 (0.83), 3.316(10.74), 3.723 (14.19), 3.821 (16.00), 7.246 (1.92), 7.268 (5.18), 7.291(5.16), 7.314 (1.92), 7.638 (2.40), 7.652 (2.79), 7.660 (3.40), 7.667(1.74), 7.674 (2.63), 7.682 (3.15), 7.695 (2.35), 7.703 (2.16), 7.717(2.08), 7.736 (4.04), 7.739 (3.93), 7.754 (1.36), 7.865 (2.10), 7.884(1.68), 7.975 (1.95), 7.983 (2.19), 7.989 (2.32), 7.997 (3.16), 8.007(0.55), 8.044 (0.51), 8.055 (3.24), 8.063 (2.31), 8.069 (2.20), 8.076(1.92), 10.309 (3.44).

Intermediate 102-[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-1H-isoindole-1,3(2H)-dione

The desired product was obtained out of the regioisomeric separationdescribed in the experimental procedure of the synthesis of2-[4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dionein 24% yield (383 mg).

LC-MS (method 10): Rt=1.98 min; MS (ESIpos): m/z=350 [M+H]⁺

¹H-NMR (400MHz, DMSO-d6): δ [ppm]: 0.82 (t, 3H), 2.23 (q, 2H), 3.73 (s,3H), 7.35-7.44 (m, 2H), 7.56-7.62 (m, 2H), 7.91-7.98 (m, 2H), 7.99-8.06(m, 2H).

Intermediate 11 4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine

A solution of2-[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-1H-isoindole-1,3(2H)-dione(380 mg, 1.09 mmol) in ethanol (7.5 mL) was treated with hydrazinehydrate (1:1) (260 μl, 5.4 mmol). The mixture was refluxed overnight.After cooling to room temperature a precipitate occurred this wasfiltered off. The filtrate was concentrated under reduced pressure andthe crude product was purified by preparative HPLC (method: column:Reprosil C18; 10 μm; 125×30 mm/flow: 50 ml/min/eluent: A=water (0.01%formic acid), B=acetonitrile/gradient: 0.00-5.00 min=10% B, 6.50 min=20%B, 17.0-19.75 min=100% B, 19.75-23.00 min=90% B) to obtain 142.6 mg (57%yield) of the desired product.

LC-MS (method 9): R_(t)=0.71 min; MS (ESIpos): m/z=220 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.905 (7.15), 0.924 (16.00), 0.943(7.20), 2.165 (2.18), 2.184 (6.66), 2.203 (6.43), 2.221 (1.95), 3.580(0.87), 7.296 (2.64), 7.301 (1.18), 7.318 (7.81), 7.324 (1.99), 7.335(1.62), 7.340 (5.83), 7.346 (1.22), 7.354 (1.05), 7.360 (5.70), 7.366(2.29), 7.374 (6.24), 7.382 (3.70), 7.391 (1.32), 7.396 (2.55), 8.139(1.15).

Intermediate 12 4-ethyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-amine

The desired product was prepared in the same manner as described for thesynthesis of 4-ethyl-5-(4-fluorophenyl)-1-methy 1-1H-pyrazol-3-aminestarting from2-[4-ethyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(307 mg, 879 μmol) to yield 68.9 mg of the desired product (36% yield).

LC-MS (method 9): R_(t)=0.63 min; MS (ESIpos): m/z=220 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.976 (7.01), 0.995 (16.00), 1.013(7.22), 2.398 (2.16), 2.416 (6.63), 2.435 (6.45), 2.454 (2.01), 3.326(0.79), 3.376 (0.45), 4.995 (1.25), 7.168 (4.18), 7.190 (8.66), 7.212(4.68), 7.517 (0.63), 7.524 (4.99), 7.530 (2.17), 7.539 (5.62), 7.546(5.07), 7.555 (1.95), 7.560 (4.38), 8.135 (0.94).

Intermediate 136-chloro-N[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]pyrimidin-4-amine

A solution of 4,6-dichloropyrimidine (1.00 g, 6.71 mmol) and4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (1.47 g, 6.71mmol) in DMF (10 mL) was treated with N,N-diisopropylethylamine (1.3 ml,7.4 mmol) and sodium iodide (1.21 g, 8.05 mmol). The resulting mixturewas stirred overnight at 80° C. DMF was removed under reduced pressure.The residue was diluted with ethyl acetate and washed with water andbrine. The organic phase was dried over sodium sulfate and the solventwas removed under reduced pressure. After trituration of the crudeproduct with diethylether and MTBE the desired pure product wasobtained. Preparative HPLC (method: column: Reprosil C18; 10 μm; 125×30mm/flow: 50 ml/min/eluent: A=water (0.01% formic acid),B=acetonitrile/gradient: 0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75min=100% B, 19.75-23.00 min=90% B) of the filtrate yielded additionalproduct. Overall 922 mg of the desired product (41% yield) wereobtained.

LC-MS (method 10): R_(t)=1.88 min; MS (ESIpos): m/z=332 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.855 (3.17), 0.874 (7.29), 0.892(3.31), 2.281 (0.84), 2.300 (2.49), 2.319 (2.43), 2.337 (0.80), 2.734(13.43), 2.894 (16.00), 3.320 (10.85), 7.108 (1.02), 7.354 (1.69), 7.376(3.82), 7.398 (2.27), 7.490 (2.35), 7.496 (1.05), 7.504 (2.67), 7.511(2.00), 7.521 (0.89), 7.525 (1.67), 7.956 (2.14), 8.416 (2.81), 9.700(1.21).

Intermediate 14N-[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-hydrazinylpyrimidin-4-amine

A solution of6-chloro-N-[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]pyrimidin-4-amine(645 mg, 1.94 mmol) in 1,4-dioxane (13 mL) was treated with hydrazinehydrate (1:1) (280 5.8 mmol). The resulting mixture was stirredovernight at 70° C. The solvent was removed under reduced pressure. Theresidue was triturated with acetonitrile to yield 574 mg (90% yield) ofthe desired product.

LC-MS (method 10): R_(t)=1.07 min; MS (ESIpos): m/z=328 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.87 (t, 3H), 2.29 (q, 2H), 3.62 (s,3H), 6.27 (s, 1H), 6.90 (br s, 2H), 7.28-7.42 (m, 2H), 7.46-7.55 (m,2H), 7.69 (br s, 1H), 7.88-7.97 (m, 1H), 8.38 (s, 1H).

Intermediate 15 2-cyclopropyl-3-(4-fluorophenyl)-3-oxopropanenitrile

Lithium diisopropylamide (34 ml, 2.0 M, 68 mmol in THF) is cooled to−78° C. Then, cyclopropylacetonitrile (5.7 ml, 62 mmol) in 50 mL of THFwas slowly added at this temperature. The reaction mixture was stirredat this temperature for 10 min and then, a solution of 4-fluorobenzoylchloride (4.0 ml, 34 mmol) in 50 mL THF was added dropwise. The reactionmixture was allowed to reach room temperature and stirred for 10 min. A2 M hydrochloric acid solution was carefully added. Then, ethyl acetatewas added. The aqueous layer was extracted 3 times with ethyl acetate.The organic phases were gathered, dried over magnesium sulfate andconcentrated under vacuum. The crude product was purified by flashcolumn chromatography on silica gel using cyclohecane/ethyl aceate toafford 4.36 g (75% purity, 47% yield) of the desired product.

LC-MS (method 11): R_(t)=1.17 min; MS (ESIneg): m/z=202 [M−H]⁻

Intermediate 16 4-cyclopropyl-5-(4-fluorophenyl)-1H-pyrazol-3-amine

The described example was prepared in the same manner as described inthe synthesis of 4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-amine startingfrom 2-cyclopropyl-3-(4-fluorophenyl)-3-oxopropanenitrile (4.36 g, 18.4mmol) to obtain 4.49 g (78% purity, 88% yield) of the desired productwhich was used in the next step without any further purification.

LC-MS (method 11): R_(t)=0.90 min; MS (ESIpos): m/z=218 [M+H]⁺

Intermediate 172-[4-cyclopropyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]-1H-isoindole-1,3(2H)-dione

The described example was prepared in the same manner as described inthe synthesis of2-[4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dionestarting from 4-cyclopropyl-5-(4-fluorophenyl)-1H-pyrazol-3-amine (4.1g, 14.7 mmol) to obtain 7.44 g (68% purity, 99% yield) of the desiredproduct which was used in the next step without any furtherpurification.

LC-MS (method 11): Rt=1.28 min; MS (ESIpos): m/z=348 [M+H]⁺

Intermediate 182-[4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-1H-isoindole-1,3(2H)-dione

A solution of2-[4-cyclopropyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]-1H-isoindole-1,3(2H)-dione(7.44 g, 68% purity, 14.6 mmol) in DMF (35 mL) was treated withpotassium carbonate (4.03 g, 29.1 mmol) and iodomethane (1.8 ml, 29mmol). The mixture was stirred at room temperature for 20 hours. Ethylacetate and water were added. The aqueous layer was extracted with ethylacetate twice. The organic phases were gathered, dried over magnesiumsulfate and concentrated under vacuum. Diethyl ether was added to thebrown oily solid and the white precipitate was filtered to afford thedescribed regioisomer. The filtrate was concentrated and purified byflash column chromatography on silica gel using cyclohexane/ethylacetate to afford both regioisomers. The product was obtained in 31%yield (1.63 g)

LC-MS (method 11): R_(t)=1.37 min; MS (ESIpos): m/z=362 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.007 (3.24), 0.011 (3.22), 0.020(3.27), 0.024 (2.82), 0.034 (0.95), 0.448 (0.90), 0.458 (2.50), 0.462(2.48), 0.468 (1.33), 0.479 (2.62), 0.483 (2.44), 0.494 (0.82), 1.474(0.76), 1.481 (0.80), 1.486 (0.54), 1.494 (1.39), 1.502 (0.53), 1.507(0.76), 1.515 (0.69), 3.739 (0.90), 3.753 (16.00), 7.374 (1.91), 7.396(4.06), 7.418 (2.30), 7.622 (2.40), 7.636 (2.73), 7.643 (2.44), 7.657(1.99), 7.960 (2.30), 7.968 (2.69), 7.974 (2.88), 7.982 (3.93), 7.992(0.79), 8.021 (0.85), 8.031 (3.87), 8.039 (2.77), 8.045 (2.57), 8.052(2.15).

Intermediate 192-[4-cyclopropyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione

The described regioisomer was obtained in 34% yield out of theseparation of the regioisomeric mixture in the synthesis of2-[4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-1H-isoindole-1,3(2H)-dione(1.77 g).

LC-MS (method 11): Rt=1.42 min; MS (ESIpos): m/z=362 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.009 (2.94), 0.007 (2.77), 0.060(2.44), 0.069 (2.50), 0.653 (1.99), 0.658 (1.97), 0.673 (2.07), 0.678(1.95), 1.680 (1.16), 2.327 (0.58), 2.669 (0.60), 3.735 (16.00), 7.265(2.01), 7.287 (4.10), 7.309 (2.13), 7.889 (2.15), 7.903 (2.34), 7.911(2.28), 7.925 (2.03), 7.997 (2.44), 8.005 (2.61), 8.011 (2.52), 8.018(3.77), 8.081 (3.91), 8.088 (2.61), 8.094 (2.67), 8.102 (2.40).

Intermediate 204-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine

The desired product was obtained in the same manner as described for thesynthesis of 4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-aminestarting from2-[4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-1H-isoindole-1,3(2H)-dione(1.64 g, 4.53 mmol) to yield 1.02 g (97% yield) of the desired product.

LC-MS (method 11): R_(t)=1.03 min; MS (ESIpos): m/z=232 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (0.45), 0.008 (0.41), 0.037(0.74), 0.047 (2.30), 0.052 (2.43), 0.060 (2.62), 0.065 (2.27), 0.074(0.81), 0.514 (0.80), 0.523 (2.14), 0.528 (2.14), 0.534 (1.03), 0.538(0.99), 0.544 (2.22), 0.549 (2.14), 0.559 (0.74), 1.396 (0.65), 1.403(0.67), 1.408 (0.41), 1.416 (1.21), 1.424 (0.40), 1.429 (0.63), 1.436(0.59), 3.417 (16.00), 3.538 (0.48), 4.351 (3.94), 7.281 (1.70), 7.286(0.63), 7.298 (0.86), 7.304 (3.89), 7.309 (0.85), 7.320 (0.73), 7.326(2.32), 7.419 (2.34), 7.425 (0.95), 7.433 (2.58), 7.441 (1.94), 7.450(0.75), 7.455 (1.66).

Intermediate 214-cyclopropyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-amine

The desired product was obtained in the same manner as described for thesynthesis of 4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-aminestarting from2-[4-cyclopropyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(1.77 g, 4.90 mmol) to yield 1.09 g (96% yield) of the desired product.

LC-MS (method 11): Rt=0.96 min; MS (ESIpos): m/z=233 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.149 (2.50), 0.159 (7.93), 0.163(8.80), 0.172 (8.96), 0.176 (8.13), 0.186 (2.67), 0.751 (2.50), 0.760(7.11), 0.765 (7.18), 0.770 (3.80), 0.780 (7.55), 0.785 (7.29), 0.795(2.47), 1.511 (1.10), 1.523 (2.29), 1.530 (2.39), 1.536 (1.63), 1.543(4.28), 1.550 (1.58), 1.556 (2.28), 1.563 (2.14), 1.576 (0.95), 2.270(0.44), 3.319 (7.71), 3.364 (0.45), 3.746 (0.55), 4.911 (16.00), 7.141(0.81), 7.148 (6.92), 7.170 (14.33), 7.193 (7.73), 7.756 (0.92), 7.763(7.61), 7.768 (3.32), 7.777 (8.56), 7.785 (8.45), 7.794 (3.04), 7.799(7.27).

Intermediate 224-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine

The desired product was prepared in the same manner as described in thesynthesis of 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidinestarting from 4,6-dichloropyrimidine (2.00 g, 13.4 mmol) and4-chloro-3,5-dimethyl-1H-pyrazole (1.75 g, 13.4 mmol) to yield 2.16 g(66% yield) of the desired product.

LC-MS (method 9): Rt=1.19 min; MS (ESIpos): m/z=244 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 2.060 (0.07), 2.092 (0.09), 2.255(16.00), 2.277 (0.21), 2.327 (0.12), 2.366 (0.04), 2.414 (0.09), 2.665(15.71), 2.699 (0.19), 2.730 (0.04), 2.827 (0.09), 2.889 (0.04), 5.290(0.04), 7.912 (2.83), 8.942 (2.94).

Intermediate 23 2-(2,4-difluorobenzoyl)butanenitrile

The desired product was prepared in the same manner as described in thesynthesis of 2-(4-fluorobenzoyl)butanenitrile starting from methyl2,4-difluorobenzoate (7.2 ml, 58 mmol) and butanenitrile (1.3 ml, 14mmol) to obtain 2.73 g (90% yield) of the desired product.

LC-MS (method 10): R_(t)=1.65 min; MS (ESIpos): m/z=210 [M+H]⁺

Intermediate 24 5-(2,4-difluorophenyl)-4-ethyl-1H-pyrazol-3-amine

The desired product was prepared in the same manner as described in thesynthesis of 4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-amine starting from2-(2,4-difluorobenzoyl)butanenitrile (2.73 g, 13.1 mmol) to obtain 2.13g (73% yield) of the desired product.

LC-MS (method 10): R_(t)=1.18 min; MS (ESIpos): m/z=224 [M+H]⁺

Intermediate 252-{1-[2-(benzyloxy)ethyl]-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl}-1H-isoindole-1,3(2H)-dione

A solution of2-[4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(1.00 g, 2.98 mmol) in DMF (5.0 mL) was treated with benzyl 2-bromoethylether (940 μl, 6.0 mmol) and potassium carbonate (824 mg, 5.96 mmol).The resulting mixture was stirred overnight at room temperature. Themixture was poured into water and extracted with ethyl acetate. Thecombined organic phases were washed with water, brine, dried over sodiumsulfate and the solvent was removed under reduced pressure. The crudeproduct was purified by preparative HPLC (method: column: Reprosil C18;10 μm; 125×30 mm/flow: 50 ml/min/eluent: A=water (0.01% formic acid),B=acetonitrile/gradient: 0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75min=100% B, 19.75-23.00 min=90% B). The obtained regioisomeric mixturewas separated using SFC carbon dioxide/ethanol as eluting system toafford 252 mg (18% yield) of the indicated product.

LC-MS (method 10): R_(t)=2.42 min; MS (ESIpos): m/z=470 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.919 (5.80), 0.938 (12.81), 0.956(5.98), 2.446 (1.77), 2.465 (5.27), 2.484 (6.64), 3.667 (3.55), 3.681(7.47), 3.694 (3.83), 4.194 (3.73), 4.207 (6.98), 4.221 (3.33), 4.337(16.00), 5.754 (3.57), 7.126 (3.40), 7.136 (4.28), 7.144 (4.44), 7.216(8.33), 7.220 (8.53), 7.229 (4.59), 7.242 (1.07), 7.275 (3.43), 7.297(6.64), 7.319 (3.59), 7.683 (3.89), 7.697 (4.52), 7.704 (4.26), 7.718(3.50), 7.947 (3.28), 7.955 (4.02), 7.961 (4.47), 7.968 (6.43), 7.978(1.49), 7.994 (1.51), 8.004 (6.58), 8.012 (4.28), 8.018 (3.98), 8.026(3.08).

Intermediate 262-{1-[2-(benzyloxy)ethyl]-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl}-1H-isoindole-1,3(2H)-dione

The described product was obtained in 9% yield (127 mg) out of theregioisomeric separation in the preparation of2-{1-[2-(benzyloxy)ethyl]-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl}-1H-isoindole-1,3(2H)-dione.

LC-MS (method 10): Rt=2.40 min; MS (ESIpos): m/z=470 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: 0.81 (t, 3H), 2.22 (q, 2H), 3.74 (t,2H), 4.16 (t, 2H), 4.36 (s, 2H), 7.18 (d, 2H), 7.23-7.37 (m, 5H), 7.49(dd, 2H), 7.92-7.99 (m, 2H), 8.00-8.08 (m, 2H).

Intermediate 271-[2-(benzyloxy)ethyl]-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-amine

The described product was prepared in the same manner as described forthe synthesis of 4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-aminestarting from2-{1-[2-(benzyloxy)ethyl]-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl}-1H-isoindole-1,3(2H)-dione(230 mg, 490 μmol) to obtain 150 mg (90% yield) of the desired product.

LC-MS (method 10): R_(t)=1.91 min; MS (ESIpos): m/z=340 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.988 (5.85), 1.006 (13.43), 1.025(6.05), 1.909 (0.49), 2.414 (1.76), 2.433 (5.46), 2.451 (5.33), 2.470(1.65), 3.728 (3.49), 3.743 (8.09), 3.757 (3.99), 4.107 (4.00), 4.121(7.83), 4.136 (3.43), 4.491 (16.00), 4.925 (8.16), 5.754 (3.70), 7.173(3.36), 7.195 (6.99), 7.217 (3.79), 7.243 (0.58), 7.249 (0.61), 7.260(2.83), 7.267 (3.62), 7.283 (10.10), 7.295 (7.24), 7.309 (3.09), 7.313(3.19), 7.330 (1.16), 7.530 (0.57), 7.537 (4.36), 7.543 (1.86), 7.552(4.94), 7.559 (4.48), 7.569 (1.72), 7.573 (3.86).

Intermediate 281-[2-(benzyloxy)ethyl]-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-amine

The described product was prepared in the same manner as described forthe synthesis of 4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-aminestarting from2-{1-[2-(benzyloxy)ethyl]-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl}-1H-isoindole-1,3(2H)-dione(125 mg, 266 μmol) to obtain 76.4 mg (85% yield) of the desired product.

LC-MS (method 10): R_(t)=1.91 min; MS (ESIpos): m/z=340 [M+H]⁺

Intermediate 29 4,4,4-trifluoro-2-(4-fluorobenzoyl)butanenitrile

A solution of 4,4,4-trifluorobutanenitrile (4.90 g, 39.8 mmol) in THF(50 mL) was treated at room temperature with lithiumbis(trimethylsilyl)amide 1M in THF (50 ml, 1.0 M, 50 mmol). To thissolution ethyl 4-fluorobenzoate (3.35 g, 19.9 mmol) was added drop wise.The reaction mixture was stirred for two days. The mixture was pouredinto water; THF was removed under reduced pressure. The aqueous phasewas extracted with MTBE and subsequently acidified by addition of 1 Mhydrochloric acid which was extracted again with MTBE. The combinedorganic phases were washed with brine; the solvent was removed underreduced pressure to obtain 5.65 g (76% yield, 66% purity) of the desiredcrude product which was used without any further purification.

LC-MS (method 11): Rt=1.19 min; MS (ESIpos): m/z=246 [M+H]⁺

Intermediate 303-(4-fluorophenyl)-4-(2,2,2-trifluoroethyl)-1H-pyrazol-5-amine

A solution of 4,4,4-trifluoro-2-(4-fluorobenzoyl)butanenitrile (5.40 g,66% purity, 14.5 mmol) in ethanol (30 mL) was treated with hydrazinehydrate (1:1) (1.8 ml, 80% purity, 29 mmol). The mixture was stirred for4 h at 90° C. and overnight at room temperature. The solvent was removedunder reduced pressure and the residue was purified by preparativereverse phase HPLC (acetonitrile/water+0.1% formic acid) to obtain 884mg of the desired product (22% yield).

LC-MS (method 11): R_(t)=1.02 min; MS (ESIpos): m/z=260 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 2.670 (0.47), 3.420 (5.54), 3.449(16.00), 3.477 (15.21), 3.504 (4.75), 4.837 (1.25), 7.234 (5.08), 7.255(9.46), 7.276 (5.57), 7.540 (11.63), 7.554 (13.43), 7.561 (12.57), 7.575(10.01), 11.814 (1.07).

Intermediate 31 4-methoxybutanenitrile

A solution of 4-bromobutanenitrile (670 μl, 6.8 mmol) in methanol (6.8mL) was treated with sodium methoxide (3.8 ml, 5.4 M, 20 mmol). Themixture was stirred overnight at room temperature. The solvent wasremoved under reduced pressure; the residue was diluted withwater/dichloromethane. After separation of the two layers, the aqueousphase was extracted twice with dichloromethane. The combined organicphases were dried over sodium sulfate and the solvent was removed underreduced pressure to obtain 594 mg (89% yield) of the desired product.

Intermediate 32 2-(4-fluorobenzoyl)-4-methoxybutanenitrile

The desired product was prepared in the same manner as described for thesynthesis of 2-(4-fluorobenzoyl)butanenitrile starting from4-methoxybutanenitrile (590 mg, 5.95 mmol) and ethyl 4-fluorobenzoate(3.5 ml, 24 mmol) to obtain 1.22 g (95% yield) of the desired product.

LC-MS (method 10): R_(t)=1.54 min; MS (ESIneg): m/z=220 [M−H]⁻

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.014 (1.27), −0.008 (4.21), −0.006(3.87), 0.008 (3.01), 2.052 (0.61), 2.067 (0.81), 2.074 (0.41), 2.087(0.67), 2.137 (0.69), 2.155 (0.79), 2.168 (0.64), 2.172 (0.45), 3.188(16.00), 3.275 (7.84), 3.453 (1.22), 3.458 (2.12), 3.467 (2.23), 3.471(1.76), 3.475 (3.16), 3.482 (1.14), 3.491 (1.24), 5.131 (0.98), 5.144(1.10), 5.152 (1.05), 5.165 (0.93), 7.295 (0.90), 7.300 (1.40), 7.305(0.51), 7.317 (2.15), 7.322 (2.62), 7.339 (1.36), 7.344 (1.34), 7.404(1.58), 7.410 (0.59), 7.427 (3.17), 7.444 (0.60), 7.449 (1.69), 7.579(0.90), 7.585 (0.41), 7.593 (0.96), 7.601 (0.86), 7.615 (0.78), 7.985(1.11), 7.990 (0.44), 7.999 (1.18), 8.007 (1.19), 8.016 (0.44), 8.021(1.09), 8.056 (1.71), 8.061 (0.77), 8.069 (1.83), 8.078 (1.80), 8.086(0.72), 8.092 (1.63), 10.988 (1.28).

Intermediate 33 5-(4-fluorophenyl)-4-(2-methoxyethyl)-1H-pyrazol-3-amine

The desired product was prepared in the same manner as described for thesynthesis of 4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-amine starting from2-(4-fluorobenzoyl)-4-methoxybutanenitrile (1.22 g, 5.51 mmol) to obtain953 mg (73% yield) of the desired product.

LC-MS (method 10): R_(t)=1.03 min; MS (ESIpos): m/z=236 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 2.598 (1.60), 2.616 (3.31), 2.633(1.70), 3.222 (16.00), 3.387 (1.53), 7.259 (1.13), 7.525 (1.25), 7.540(1.63), 7.559 (1.10).

Intermediate 34 1-(6-chloropyrimidin-4-yl)-3-methyl-1H-indazole

A solution of 4,6-dichloropyrimidine (1.13 g, 7.57 mmol) and3-methyl-1H-indazole (1.00 g, 7.57 mmol) in DMF (10 mL) was treated withcaesium carbonate (2.47 g, 7.57 mmol) and stirred over the weekend atroom temperature. Water was added and the resulting mixture was stirredat room temperature for 30 min. The precipitate was filtered, washedwith water and dried under reduced pressure to afford 1.55 g (84% yield)of the desired product which contained minor amounts of theregioisomeric product.

LC-MS (method 11): R_(t)=1.50 min; MS (ESIpos): m/z=245 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 2.327 (0.09), 2.365 (0.09), 2.456(0.11), 2.619 (16.00), 2.670 (0.18), 2.709 (0.09), 2.778 (0.09), 3.035(0.89), 3.097 (0.09), 7.072 (0.10), 7.093 (0.09), 7.362 (0.10), 7.377(0.09), 7.408 (1.15), 7.426 (2.35), 7.445 (1.46), 7.593 (0.14), 7.616(0.13), 7.638 (1.25), 7.658 (2.00), 7.677 (1.15), 7.773 (0.13), 7.794(0.13), 7.897 (2.29), 7.912 (3.32), 8.280 (0.17), 8.685 (1.81), 8.706(1.75), 8.960 (2.96), 9.100 (0.18).

Intermediate 35 3-(2,4-difluorophenyl)-1H-pyrazol-5-amine

A solution of 3-(2,4-difluorophenyl)-3-oxopropanenitrile (9.00 g, 49.7mmol, synthesis described e.g. in J. Med. Chem. 1079, 22(11), 1385) inethanol was treated with hydrazine hydrate (1:1) (2.9 ml, 60 mmol). Themixture was refluxed for 3.5 h. After cooling to room temperaturesaturated sodium hydrogen carbonate solution was added, ethanol wasremoved under reduced pressure and the residue was extracted with ethylacetate. The combined organic phases were washed with brine, dried oversodium sulfate and the solvent was removed under reduced pressure toyield 8.36 g (77% yield) of the desired product which was used withoutany further purification.

LC-MS (method 9): R_(t)=0.53 min; MS (ESIpos): m/z=196 [M+H]⁺

Intermediate 36 4-chloro-3-(2,4-difluorophenyl)-1H-pyrazol-5-amine

A solution of 3-(2,4-difluorophenyl)-1H-pyrazol-5-amine (2.30 g, 11 8mmol) in acetonitrile (20 mL) was treated with1-chloropyrrolidine-2,5-dione (1.57 g, 11.8 mmol and stirred at roomtemperature for 30 min. The mixture was diluted with water and extractedwith ethyl acetate. The combined organic phases were washed with waterand brine, dried over sodium sulfate and the solvent was removed underreduced pressure to yield 2.53 g (93% yield) of the desired crudeproduct which was used without any further purification.

LC-MS (method 10): R_(t)=1.32 min; MS (ESIpos): m/z=230 [M+H]⁺

Intermediate 372-[4-chloro-3-(2,4-difluorophenyl)-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione

4-chloro-3-(2,4-difluorophenyl)-1H-pyrazol-5-amine (1.97 g, 8.56 mmol)and 2-benzofuran-1,3-dione (1.90 g, 12.8 mmol) in acetic acid (25 mL)were reflux overnight. Acetic acid was removed under reduced pressure.The residue was partitioned between brine and ethyl acetate. The organicphase wash dried over sodium sulfate and the solvent was removed underreduced pressure. The crude product was triturated with MTBE to yielddesired product. The filtrate was further purified by preparative HPLC(Sunfire C18 5 μm, 75×30 mm, flow 80 mL/min, 40° C., 210 nM, eluent A:water, eluent B: water +1% formic acid, eluent C: acetonitrile,gradient: 0-1 min at 60/5/35 A/B/C, 1-5 min to 47.5/5/47.5, 5.0-5.31 minto 0/5/95, 5.31-6.74 at 0/5/95). In total 2.02 g (63.7% yield) of thedesired product were obtained.

LC-MS (method 10): R_(t)=1.84 min; MS (ESIpos): m/z=360 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 7.23-7.40 (m, 1H), 7.49-7.63 (m, 1H),7.76 (td, 1H), 7.92-8.11 (m, 4H), 14.07 (s, 1H).

Intermediate 382-[4-chloro-3-(2,4-difluorophenyl)-1-methyl-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione

A solution of2-[4-chloro-3-(2,4-difluorophenyl)-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(1.50 g, 4.17 mmol) in DMF (10 mL) was treated with iodomethane (520 μl,8.3 mmol) and potassium carbonate (1.15 g, 8.34 mmol). The mixture wasstirred for 3 hours at room temperature. The mixture was partitionedbetween water and ethyl acetate. The organic layer was washed with brineand dried over sodium sulfate. After removal of the solvent underreduced pressure, the regioisomers were separated using preparative HPLC(Daicel Chiralpeak ID 5 μM 20×250 mm, flow: 80 mL/min, detection at 210nm, 40° C., 0.0-8.0 min at 81% carbon dioxide/9% methanol). To yield446.4 mg (27% yield) of the desired product.

LC-MS (method 11): R_(t)=1.41 min; MS (ESIpos): m/z=374 [M+H]⁺

Intermediate 392-[4-chloro-5-(2,4-difluorophenyl)-1-methyl-1H-pyrazol-3-yl]-1H-isoindole-1,3(2H)-dione

The desired regioisomer was obtained by the regioisomeric separation inthe synthesis of2-[4-chloro-3-(2,4-difluorophenyl)-1-methyl-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione.788 mg (50% yield) of the desired product were yielded.

LC-MS (method 11): Rt=1.36 min; MS (ESIpos): m/z=374 [M+H]⁺

Intermediate 404-chloro-3-(2,4-difluorophenyl)-1-methyl-1H-pyrazol-5-amine

A solution of2-[4-chloro-3-(2,4-difluorophenyl)-1-methyl-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(446 mg, 1.19 mmol) in ethanol (15 mL) was treated with hydrazinehydrate (1:1) (290 μl, 6.0 mmol) and stirred for 1 h at 80° C. Aftercooling to room temperature, the precipitate was removed by filtration.The filtrate was taken to dryness to yield the desired product (281 mg,97% yield).

LC-MS (method 11): R_(t)=1.06 min; MS (ESIpos): m/z=244 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 3.317 (16.00), 5.536 (6.97), 7.119(0.75), 7.124 (0.81), 7.140 (1.58), 7.146 (1.68), 7.161 (0.88), 7.167(0.92), 7.288 (0.92), 7.294 (0.87), 7.312 (1.43), 7.318 (1.39), 7.337(0.95), 7.344 (0.88), 7.469 (1.00), 7.487 (1.29), 7.491 (1.96), 7.508(1.98), 7.511 (1.12), 7.529 (0.92).

Intermediate 414-chloro-5-(2,4-difluorophenyl)-1-methyl-1H-pyrazol-3-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation of4-chloro-3-(2,4-difluorophenyl)-1-methyl-1H-pyrazol-5-amine startingfrom2-[4-chloro-5-(2,4-difluorophenyl)-1-methyl-1H-pyrazol-3-yl]-1H-isoindole-1,3(2H)-dione(788 mg, 2.11 mmol) to yield 384 mg of the desired product (75% yield).

LC-MS (method 11): R_(t)=1.06 min; MS (ESIpos): m/z=244 [M+H]⁺

¹H-NMR (500 MHz, DMSO-d₆) δ [ppm]: −0.007 (1.21), 0.006 (0.99), 2.521(0.42), 3.321 (16.00), 4.913 (12.76), 7.259 (1.43), 7.263 (1.51), 7.276(3.00), 7.280 (3.06), 7.293 (1.64), 7.297 (1.68), 7.464 (1.99), 7.469(1.97), 7.483 (2.79), 7.484 (2.83), 7.488 (2.76), 7.503 (2.05), 7.508(1.99), 7.521 (2.04), 7.534 (2.43), 7.538 (3.83), 7.551 (3.83), 7.555(2.11), 7.568 (1.79).

Intermediate 42-1 3-(4-fluorophenyl)-1H-pyrazol-5-amine

A solution of 3-(4-fluorophenyl)-3-oxopropanenitrile (470 mg, 60%purity, 1.73 mmol, CAS 4640-67-9) in ethanol (3.6 mL) was treated withhydrazine hydrate (1:1) (100 μl, 2.1 mmol). The mixture was refluxed for3 h and stirred over the weekend at room temperature. The mixture wasdiluted with started sodium hydrogen carbonate solution, ethanol wasremoved under reduced pressure. The resulting precipitate was collectedby filtration. The filtrate was also taken to dryness and combined withthe precipitate to yield 360 mg of a approx. 2:1 mixture of3-(4-fluorophenyl)-1H-pyrazol-5-amine together with3-(4-ethoxyphenyl)-1H-pyrazol-5-amine The mixture was used in the nextreaction.

LC-MS (method 10): R_(t)=0.87 min; MS (ESIpos): m/z=178[M+H]⁺/R_(t)=0.97 min; MS (ESIpos): m/z=204 [M+H]⁺

Intermediate 42-2 3-(4-ethoxyphenyl)-1H-pyrazol-5-amine

A solution of 3-(4-fluorophenyl)-3-oxopropanenitrile (470 mg, 60%purity, 1.73 mmol, CAS 4640-67-9) in ethanol (3.6 mL) was treated withhydrazine hydrate (1:1) (100 μl, 2.1 mmol). The mixture was refluxed for3 h and stirred over the weekend at room temperature. The mixture wasdiluted with started sodium hydrogen carbonate solution, ethanol wasremoved under reduced pressure. The resulting precipitate was collectedby filtration. The filtrate was also taken to dryness and combined withthe precipitate to yield 360 mg of a approx. 2:1 mixture of3-(4-fluorophenyl)-1H-pyrazol-5-amine together with3-(4-ethoxyphenyl)-1H-pyrazol-5-amine. The mixture was used in the nextreaction.

LC-MS (method 10): R_(t)=0.87 min; MS (ESIpos): m/z=178[M+H]⁺/R_(t)=0.97 min; MS (ESIpos): m/z=204 [M+H]⁺

Intermediate 43 4-chloro-3-(4-fluorophenyl)-1H-pyrazol-5-amine

A solution of 3-(4-fluorophenyl)-1H-pyrazol-5-amine (100 mg, 564 μmol,mixture with the ethoxy-by product out of the step before) inacetonitrile (1.1 ml, 20 mmol) was treated with1-chloropyrrolidine-2,5-dione (75.4 mg, 564 μmol). The mixture wasstirred 30 min at room temperature. Water was added and the mixture wasthree times extracted with ethyl acetate. The combined organic phaseswere washed with water and brine, dried over sodium sulfate and thesolvent was removed under reduced pressure. The crude product waspurified by preparative HPLC (method 7) to yield 36 mg (30% yield) ofthe desired product. The corresponding ethoxy-derivative was alsoisolated.

LC-MS (method 10): R_(t)=1.31 min; MS (ESIpos): m/z=212 [M+H]⁺

Intermediate 44 4-chloro-3-(4-ethoxyphenyl)-1H-pyrazol-5-amine

The desired product was obtained by the separation of the two componentsin the synthesis of 4-chloro-3-(4-fluorophenyl)-1H-pyrazol-5-amine in20% yield (27 mg).

LC-MS (method 10): R_(t)=1.42 min; MS (ESIpos): m/z=238 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: 1.34 (t, 3H), 4.07 (q, 2H), 4.74 (s,2H), 7.03 (br d, 2H), 7.63 (br d, 2H), 12.06 (s, 1H).

Intermediate 45 2-methyl-3-oxo-3-phenylpropanenitrile

A solution of propanenitrile (3.0 ml, 42 mmol) in THF (130 mL) wastreated with lithium bis(trimethylsilyl)amide 1M in THF (120 mL, 1.0 M,120 mmol). Subsequently ethyl benzoate (24 ml, 170 mmol) was added atroom temperature. The mixture was stirred for 4 hours at roomtemperature. Water was added and the mixture was extracted withdichloromethane. The combined organic phases were discarded. The aqueousphase was acidified with aqueous hydrochloric acid and extracted withdichloromethane. The organic phase was washed with water, brine anddried over sodium sulfate. After removal of the solvent under reducedpressure 7.83 g (98% yield) of the desired product were obtained.

LC-MS (method 10): R_(t)=1.43 min; MS (ESIpos): m/z=160 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 1.485 (15.70), 1.503 (16.00), 1.679(2.50), 1.876 (11.52), 1.878 (13.95), 5.125 (1.69), 5.142 (5.29), 5.160(5.26), 5.178 (1.64), 7.420 (0.40), 7.429 (0.41), 7.462 (0.76), 7.473(3.07), 7.477 (3.42), 7.485 (6.48), 7.490 (7.04), 7.496 (1.65), 7.500(1.30), 7.505 (2.29), 7.525 (1.49), 7.547 (1.82), 7.549 (2.38), 7.552(2.14), 7.555 (2.00), 7.559 (2.21), 7.565 (1.64), 7.569 (1.70), 7.571(1.78), 7.574 (1.47), 7.582 (3.45), 7.586 (1.47), 7.600 (7.32), 7.620(5.31), 7.711 (2.34), 7.714 (1.39), 7.729 (3.48), 7.748 (1.35), 7.751(0.75), 7.956 (0.68), 7.960 (1.26), 7.964 (1.23), 7.977 (0.93), 7.981(1.24), 8.031 (6.27), 8.050 (6.00), 10.835 (3.58).

Intermediate 46 4-methyl-3-phenyl-1H-pyrazol-5-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation of4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-amine starting from2-methyl-3-oxo-3-phenylpropanenitrile (7.83 g, 83% purity, 40.8 mmol) toyield 3.47 g of the desired product 49% yield).

LC-MS (method 10): R_(t)=0.89 min; MS (ESIpos): m/z=174 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.007 (0.91), 1.983 (16.00), 4.467(1.03), 7.299 (1.65), 7.313 (1.32), 7.418 (3.61), 7.514 (3.90), 7.531(3.04), 11.566 (0.82).

Intermediate 47 3-(4-fluorophenyl)-2-methyl-3-oxopropanenitrile

The described product was prepared in a manner analogous to thatdescribed in the preparation of 2-methyl-3-oxo-3-phenylpropanenitrilestarting from propanenitrile (6.4 ml, 89 mmol) and ethyl4-fluorobenzoate (4.4 ml, 30 mmol) to yield 4.12 g of the desiredproduct (77% yield).

LC-MS (method 10): R_(t)=1.49 min; MS (ESIpos): m/z=178 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 1.493 (15.61), 1.511 (16.00), 1.688(1.74), 1.881 (12.92), 2.560 (1.31), 5.125 (1.23), 5.143 (3.77), 5.161(3.74), 5.179 (1.20), 7.296 (1.59), 7.318 (3.35), 7.340 (1.84), 7.412(3.38), 7.434 (6.92), 7.455 (3.62), 7.617 (1.92), 7.631 (2.22), 7.638(2.09), 7.652 (1.71), 8.121 (4.30), 8.135 (4.95), 8.143 (4.78), 8.157(4.13), 10.881 (2.02).

Intermediate 48 3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation of 4-methyl-3-phenyl-1H-pyrazol-5-aminestarting from 3-(4-fluorophenyl)-2-methyl-3-oxopropanenitrile (4.10 g,23.1 mmol) to yield 3.86 g of the desired product (86% yield).

LC-MS (method 10): R_(t)=0.98 min; MS (ESIpos): m/z=192 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 1.931 (0.42), 1.965 (16.00), 3.336(1.15), 4.451 (0.49), 7.258 (1.43), 7.554 (1.59), 11.570 (0.45).

Intermediate 49 2-(4-chlorobenzoyl)butanenitrile

The described product was prepared in a manner analogous to thatdescribed in the preparation of 2-methyl-3-oxo-3-phenylpropanenitrilestarting from butanenitrile (710 μl, 8 2 mmol) and methyl4-chlorobenzoate (5.56 g, 32.6 mmol) to yield 1.57 g of the desiredproduct (93% yield).

LC-MS (method 10): R_(t)=1.83 min; MS (ESIpos): m/z=208 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.989 (7.60), 1.008 (16.00), 1.026(7.89), 1.057 (2.39), 1.076 (4.91), 1.095 (2.44), 1.763 (0.90), 1.782(1.44), 1.798 (1.75), 1.817 (2.06), 1.835 (1.34), 1.922 (1.28), 1.935(1.40), 1.941 (1.51), 1.945 (0.92), 1.953 (1.53), 1.957 (1.42), 1.970(1.07), 1.975 (1.01), 1.989 (0.79), 2.270 (0.79), 2.289 (2.33), 2.308(2.25), 2.327 (0.80), 5.136 (2.44), 5.149 (2.73), 5.156 (2.68), 5.169(2.39), 7.421 (0.62), 7.538 (1.06), 7.544 (1.16), 7.551 (5.96), 7.558(10.61), 7.563 (3.37), 7.575 (2.31), 7.580 (6.97), 7.654 (1.07), 7.660(6.98), 7.665 (3.09), 7.677 (2.78), 7.682 (8.02), 7.688 (1.36), 7.924(0.92), 7.930 (6.97), 7.935 (2.27), 7.947 (2.05), 7.952 (6.41), 8.015(1.34), 8.022 (8.65), 8.026 (3.25), 8.038 (2.87), 8.043 (7.78), 8.049(1.16).

Intermediate 50 5-(4-chlorophenyl)-4-ethyl-1H-pyrazol-3-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation of 4-methyl-3-phenyl-1H-pyrazol-5-aminestarting from 2-(4-chlorobenzoyl)butanenitrile (1.57 g, 7.54 mmol) toyield 1.39 g of the desired product (83% yield).

LC-MS (method 10): R_(t)=1.36 min; MS (ESIpos): m/z=222 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (1.07), 0.008 (1.06), 0.966(0.72), 0.981 (0.63), 0.984 (0.66), 1.000 (1.93), 1.011 (7.53), 1.030(16.00), 1.049 (8.81), 2.367 (0.57), 2.399 (3.87), 2.418 (12.08), 2.437(11.78), 2.455 (3.63), 3.291 (0.63), 3.509 (2.51), 4.444 (1.13), 7.432(3.66), 7.435 (1.93), 7.490 (10.19), 11.600 (1.36).

Intermediate 51 (4-fluorobenzoyl)propanedinitrile

To sodium hydride (2.52 g, 60% purity, 63.1 mmol) in THF (10 mL) at 0 to5° C. a solution of propanedinitrile (2.08 g, 31.5 mmol) in THF (10 mL)was added dropwise. The mixture was stirred for 15 minutes, subsequently4-fluorobenzoyl chloride (3.7 ml, 32 mmol) was added. The mixture wasallowed to warm up to room temperature and stirred for 1 hour. Themixture was acidified to pH1 and extracted two times with ethyl acetate.The combined organic phases were dried over sodium sulfate, the solventwas removed under reduced pressure. The crude product was trituratedfrom MTBE to yield 4.15 g (67% yield) of the desired product.

LC-MS (method 9): R_(t)=0.49 min; MS (ESIneg): m/z=187 [M−H]⁻

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (1.19), 0.008 (1.10), 1.175(0.51), 1.988 (0.99), 3.575 (2.69), 7.145 (0.89), 7.153 (7.89), 7.158(2.62), 7.169 (3.36), 7.175 (16.00), 7.180 (3.22), 7.192 (2.84), 7.197(8.67), 7.204 (0.99), 7.605 (0.93), 7.612 (8.57), 7.617 (3.25), 7.626(9.32), 7.634 (8.54), 7.643 (3.07), 7.648 (7.91), 7.656 (0.84).

Intermediate 52 [(4-fluorophenyl)(methoxy)methylidene]propanedinitrile

To mixture of sodium hydrogen carbonate (8.45 g, 101 mmol) in water (4.0mL) and 1,4-dioxane (25 mL) (4-fluorobenzoyl)propanedinitrile (2.37 g,12.6 mmol) was added. To this mixture dimethyl sulfate (8.9 ml, 93 mmol)was added drop wise and the reaction mixture was refluxed for 2 hours.After cooling to room temperature the mixture was diluted with water andextracted with ethyl acetate. The combined organic phases were washedwith brine, dried over sodium sulfate and the solvent was removed underreduced pressure to yield 2 g (79% yield) of the desired product whichwas used without any further purification in the next step.

Intermediate 533-amino-5-(4-fluorophenyl)-1-methyl-1H-pyrazole-4-carbonitrile

A solution of [(4-fluorophenyl)(methoxy)methylidene]propanedinitrile(930 mg, 4.60 mmol) in 2-propanol (9.3 mL) was treated withmethylhydrazine (290 μl, 5.5 mmol). The reaction mixture was refluxedfor 2 days. Water was added and the mixture was extracted with ethylacetate. The combined organic phases were washed with brine, dried oversodium sulfate and the solvent was removed under reduced pressure. Thecrude regioisomeric mixture was separated via preparative HPLC (column:Daicel Chiracel OJ-H-5 5 μM, 250×20 mm, flow 80 mL/min, 92% carbondioxide/8% methanol, 40° C., detection at 210 nM) to yield 62 mg of thedesired product (5% yield).

LC-MS (method 10): R_(t)=1.23 min; MS (ESIpos): m/z=217 [M+H]⁺

¹H-NMR (500 MHz, DMSO-d₆) δ [ppm]: 3.168 (1.37), 3.178 (1.37), 3.318(13.07), 5.640 (16.00), 7.405 (1.04), 7.411 (6.70), 7.415 (2.60), 7.429(14.37), 7.442 (2.92), 7.446 (7.97), 7.452 (1.03), 7.602 (1.25), 7.608(7.98), 7.612 (3.73), 7.619 (8.71), 7.625 (7.47), 7.632 (3.17), 7.636(6.55), 7.642 (0.74).

Intermediate 545-amino-3-(4-fluorophenyl)-1-methyl-1H-pyrazole-4-carbonitrile

The desired product was obtained out of the regioisomeric separationfrom example3-amino-5-(4-fluorophenyl)-1-methyl-1H-pyrazole-4-carbonitrile in 8%yield (78.5 mg).

LC-MS (method 10): R_(t)=1.35 min; MS (ESIpos): m/z=217 [M+H]⁺

¹H-NMR (500 MHz, DMSO-d₆) δ [ppm]: 3.59 (s, 3H), 6.69 (s, 2H), 7.23-7.34(m, 2H), 7.73-7.85 (m, 2H).

Intermediate 55 2-(cyclohexylcarbonyl)butanenitrile

The described product was prepared in a manner analogous to thatdescribed in the preparation of 2-methyl-3-oxo-3-phenylpropanenitrilestarting from butanenitrile (1.3 ml, 14 mmol) and methylcyclohexanecarboxylate (8.3 ml, 58 mmol) to yield 2.13 g of the desiredproduct (82% yield).

LC-MS (method 9): R_(t)=0.96 min; MS (ESIneg): m/z=178 [M−H]⁻

Intermediate 56 5-cyclohexyl-4-ethyl-1H-pyrazol-3-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation of 4-methyl-3-phenyl-1H-pyrazol-5-aminestarting from 2-(cyclohexylcarbonyl)butanenitrile (2.13 g, 11.9 mmol) toyield 2.16 g of the desired product (94% yield).

LC-MS (method 9): R_(t)=0.62 min; MS (ESIpos): m/z=194 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.946 (6.97), 0.965 (16.00), 0.984(7.33), 1.141 (0.68), 1.149 (1.15), 1.172 (0.94), 1.180 (1.53), 1.204(0.64), 1.211 (0.95), 1.248 (1.11), 1.255 (0.75), 1.279 (2.61), 1.286(1.68), 1.311 (2.65), 1.342 (1.17), 1.374 (1.17), 1.379 (1.14), 1.405(2.65), 1.411 (2.61), 1.436 (2.57), 1.442 (2.54), 1.467 (0.92), 1.473(0.88), 1.658 (4.22), 1.686 (3.41), 1.725 (2.85), 1.757 (2.53), 2.187(2.22), 2.206 (6.79), 2.225 (6.56), 2.243 (1.99), 2.408 (0.59), 2.416(1.02), 2.425 (0.65), 2.438 (1.16), 2.446 (1.90), 2.454 (1.09), 2.468(0.69), 2.476 (1.05), 3.507 (0.47), 4.140 (1.36), 10.860 (0.46).

Intermediate 572-(4-methyl-3-phenyl-1H-pyrazol-5-yl)-1H-isoindole-1,3(2H)-dione

The described product was prepared in a manner analogous to thatdescribed in the preparation of2-[4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dionestarting from 4-methyl-3-phenyl-1H-pyrazol-5-amine (3.47 g, 20.0 mmol)to obtain 6.66 g (99% yield) of the desired product which was used inthe next step without any further purification.

LC-MS (method 10): R_(t)=1.69 min; MS (ESIpos): m/z=304 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 1.921 (1.69), 2.029 (16.00), 7.421(0.74), 7.439 (1.88), 7.457 (1.33), 7.523 (2.34), 7.543 (3.95), 7.562(2.15), 7.580 (0.94), 7.589 (1.02), 7.595 (1.01), 7.603 (1.32), 7.646(4.08), 7.665 (3.18), 7.668 (2.35), 7.673 (1.60), 7.681 (0.95), 7.687(0.92), 7.696 (0.79), 7.935 (0.56), 7.944 (2.50), 7.951 (2.80), 7.957(2.79), 7.965 (3.92), 7.975 (0.81), 8.000 (0.96), 8.012 (4.19), 8.019(2.79), 8.026 (2.55), 8.033 (2.13).

Intermediate 582-(1,4-dimethyl-3-phenyl-1H-pyrazol-5-yl)-1H-isoindole-1,3(2H)-dione

The described product was prepared in a manner analogous to thatdescribed in the preparation of2-[4-ethyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dionestarting from2-(4-methyl-3-phenyl-1H-pyrazol-5-yl)-1H-isoindole-1,3(2H)-dione (2.50g, 8.24 mmol) to obtain 1.08 g (41% yield) of the desired product.

LC-MS (method 10): R_(t)=1.87 min; MS (ESIpos): m/z=318 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 1.832 (16.00), 3.320 (10.09), 3.745(0.43), 7.491 (0.64), 7.510 (3.71), 7.529 (6.44), 7.554 (3.89), 7.571(3.37), 7.589 (1.10), 7.939 (2.61), 7.947 (3.49), 7.953 (3.69), 7.959(3.62), 8.004 (4.25), 8.012 (3.42), 8.018 (2.74), 8.025 (1.90).

Intermediate 592-(1,4-dimethyl-5-phenyl-1H-pyrazol-3-yl)-1H-isoindole-1,3(2H)-dione

The desired product was obtained in 19% yield (509 mg) out of theregioisomeric separation in the preparation of2-(1,4-dimethyl-3-phenyl-1H-pyrazol-5-yl)-1H-isoindole-1,3(2H)-dione.

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 1.830 (0.71), 1.869 (0.09), 2.030(16.00), 2.188 (0.09), 2.327 (0.05), 2.668 (0.05), 3.315 (13.69), 3.563(0.08), 3.785 (0.75), 3.915 (0.08), 5.753 (0.13), 7.345 (0.68), 7.363(1.92), 7.381 (1.39), 7.443 (2.52), 7.462 (4.21), 7.481 (2.06), 7.512(0.18), 7.530 (0.29), 7.553 (0.19), 7.571 (0.15), 7.682 (4.21), 7.700(3.54), 7.965 (2.44), 7.973 (2.91), 7.978 (3.15), 7.986 (3.91), 7.996(0.87), 8.032 (0.78), 8.042 (3.80), 8.050 (2.99), 8.056 (2.74), 8.063(2.26).

Intermediate 60 1,4-dimethyl-3-phenyl-1H-pyrazol-5-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation of4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine starting from2-(1,4-dimethyl-3-phenyl-1H-pyrazol-5-yl)-1H-isoindole-1,3(2H)-dione(1.08 g, 3.40 mmol) to obtain 404 mg (50% yield) of the desired product.

LC-MS (method 16): R_(t)=1.20 min; MS (ESIpos): m/z=188 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.006 (1.54), 1.771 (16.00), 1.808(0.74), 1.862 (1.29), 3.320 (2.48), 3.630 (1.33), 3.643 (0.74), 7.329(2.78), 7.346 (3.33), 7.349 (3.41), 7.388 (0.50), 7.407 (1.89), 7.425(1.72), 7.470 (2.64), 7.489 (3.52), 7.508 (1.32), 7.532 (0.51), 8.152(0.40).

Intermediate 61 1,4-dimethyl-5-phenyl-1H-pyrazol-3-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation of4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine starting from2-(1,4-dimethyl-5-phenyl-1H-pyrazol-3-yl)-1H-isoindole-1,3(2H)-dione(500 mg, 1.58 mmol) to obtain 161 mg (54% yield) of the desired product.

LC-MS (method 16): R_(t)=1.16 min; MS (ESIpos): m/z=188 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 1.435 (0.90), 1.455 (0.80), 1.768(0.88), 1.984 (16.00), 2.011 (0.43), 3.329 (1.15), 3.350 (0.99), 3.453(0.92), 3.644 (0.54), 4.929 (1.26), 7.224 (0.70), 7.243 (1.74), 7.260(1.28), 7.337 (2.31), 7.355 (3.86), 7.374 (1.84), 7.422 (1.05), 7.437(0.61), 7.551 (4.46), 7.571 (3.64), 7.903 (0.56), 7.923 (0.54), 8.169(1.35).

Intermediate 62 1-(4-fluorophenyl)-3,5-dimethyl-4-nitro-1H-pyrazole

A mixture of 3,5-dimethyl-4-nitro-1H-pyrazole (630 mg, 4.47 mmol),(4-fluorophenyl)boronic acid (625 mg, 4.47 mmol), copper acetate(anhydrous, 1.22 g, 6.80 mmol) and pyridine (3.6 mL) in dichloromethane(6.0 mL) was stirred with 1.0 g of molecular sieves for 2 days at roomtemperature. The reaction mixture was filtered over Celite and washedwith dichloromethane. The organic layer was washed with water. Theaqueous layer was extracted twice with dichloromethane. The combinedorganic phases were dried with sodium sulfate and evaporated undervacuum. The crude product was purified by preparative HPLC (method:column: Reprosil C18; 10 μm; 125×30 mm/flow: 45 ml/min/eluent: A=water(0.1% formic acid), B=acetonitrile/gradient: 0.00-4.25 min=10% B, 4.50min=20% B, 15.50 min=85% B, 16.00-18.50 min=100% B, 18.75-22.00 min=20%B) to afford 591 mg (56% yield) of the desired product.

LC-MS (method 11): R_(t)=1.25 min; MS (ESIpos): m/z=236 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (0.46), 2.490 (16.00), 7.416(1.59), 7.421 (0.56), 7.438 (3.34), 7.454 (0.66), 7.459 (2.02), 7.608(2.02), 7.614 (0.76), 7.620 (2.11), 7.625 (1.13), 7.631 (1.70), 7.638(0.67), 7.643 (1.58).

Intermediate 63 1-(4-fluorophenyl)-3,5-dimethyl-1H-pyrazol-4-amine

To a solution of 1-(4-fluorophenyl)-3,5-dimethyl-4-nitro-1H-pyrazole(490 mg, 2.08 mmol) in methanol (20 mL) were added iron (582 mg, 10.4mmol) and concentrated hydrochloric acid (4.9 ml). The reaction mixturewas then heated at reflux for 2 h. The reaction mixture was cooled downand neutralized with a saturated solution of sodium hydrogen carbonateand then filtered. The aqueous layer was extracted twice with ethylacetate. The organic layers were gathered, dried over magnesium sulfateand concentrated under vacuum, to afford 386 mg of the desired product(90% yield).

LC-MS (method 11): R_(t)=0.42 min; MS (ESIpos): m/z=206 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 2.104 (15.64), 2.184 (16.00), 3.317(0.72), 7.259 (2.36), 7.264 (0.86), 7.281 (4.94), 7.297 (0.99), 7.303(2.98), 7.433 (0.40), 7.441 (2.98), 7.446 (1.20), 7.453 (3.13), 7.458(1.66), 7.463 (2.49), 7.471 (0.99), 7.476 (2.25).

Intermediate 641-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylicacid

A solution of ethyl1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(400 mg, 863 μmol) in THF was treated with aqueous potassium hydroxidesolution (2.6 mL, 2.0 M, 5.2 mmol) and aqueous lithium hydroxidesolution (4.3 ml, 1.0 M, 4.3 mmol). The mixture was stirred for 4 hoursat 90° C. Additional lithium hydroxide solution (4.3 mL, 1.0 M, 4.3mmol) were added and the mixture was stirred 2 days at 90° C. Themixture was diluted with water and extracted with diethyl ether. Theaqueous layer was acidified to pH 3 with hydrochloric acid and extractedwith ethyl acetate. The organic layer was washed with brine, dried oversodium sulfate and the solvent was removed under reduced pressure toyield 310 mg (67% yield) of the desired product.

LC-MS (method 10): R_(t)=1.78 min; MS (ESIpos): m/z=436 [M+H]⁺

Intermediate 65 4-chloro-3-phenyl-1H-pyrazol-5-amine

A solution of 3-phenyl-1H-pyrazol-5-amine (4.00 g, 25.1 mmol) inacetonitrile (47 mL) was treated with 1-chloropyrrolidine-2,5-dione(3.36 g, 25.1 mmol) and stirred at room temperature for 30 min. Themixture was diluted with water and extracted with ethyl acetate. Thecombined organic phases were washed with water, brine, dried over sodiumsulfate and the solvent was removed under reduced pressure to yield 5.31g (quant.) of the desired product which was used without any furtherpurification.

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 4.63-5.43 (m, 2H), 7.24-7.59 (m, 3H),7.73 (br s, 2H), 11.72-12.33 (m, 1H).

Intermediate 66 1-(4-fluorophenyl)-3-methyl-4-nitro-1H-pyrazole

The described product was prepared in a manner analogous to thatdescribed in the preparation of1-(4-fluorophenyl)-3,5-dimethyl-4-nitro-1H-pyrazole starting from3-methyl-4-nitro-1H-pyrazole (1.00 g, 7.87 mmol) and(4-fluorophenyl)boronic acid (2.20 g, 15.7 mmol) to obtain 1.67 g crudeproduct which was used in the next step without any furtherpurification.

Intermediate 67 1-(4-fluorophenyl)-3-methyl-1H-pyrazol-4-amine

To a solution of 1-(4-fluorophenyl)-3-methyl-4-nitro-1H-pyrazole (1.67g, 7.55 mmol) in ethanol (50 mL) and ethyl acetate (50 mL) was addedpalladium on activated carbon (402 mg, 10% purity, 377 μmol) and thesuspension was stirred under a hydrogen atmosphere overnight at roomtemperature. The mixture was filtered over Celite®. The filtrate wasevaporated to yield 1.61 g (quant.) of the desired product.

LC-MS (method 12): R_(t)=3.96 min; MS (ESIpos): m/z=192 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 1.910 (0.57), 2.116 (16.00), 2.136(0.61), 2.162 (3.81), 4.038 (0.57), 7.171 (1.37), 7.194 (1.95), 7.216(3.78), 7.238 (2.01), 7.278 (0.46), 7.300 (0.92), 7.322 (0.52), 7.465(0.60), 7.477 (0.65), 7.487 (0.50), 7.499 (0.44), 7.590 (5.25), 7.615(2.42), 7.627 (2.56), 7.638 (2.23), 7.650 (1.99).

Intermediate 682-(4-chloro-3-phenyl-1H-pyrazol-5-yl)-1H-isoindole-1,3(2H)-dione

4-chloro-3-phenyl-1H-pyrazol-5-amine (2.50 g, 12.9 mmol) and2-benzofuran-1,3-dione (2.87 g, 19.4 mmol) were dissolved in acetic acid(26 mL) and heated under reflux overnight. After rotary evaporation ofall volatiles, the crude product (4.18 g, quant.) was used in the nextstep without further purification.

Intermediate 692-(4-chloro-1-methyl-3-phenyl-1H-pyrazol-5-yl)-1H-isoindole-1,3(2H)-dione

2-(4-chloro-3-phenyl-1H-pyrazol-5-yl)-1H-isoindole-1,3(2H)-dione (4.18g, 12 9 mmol) and caesium carbonate (60% purity, 14.0 g, 25.8 mmol) weredissolved in dry DMF (32 mL) and treated with iodomethane (1.6 mL, 26mmol). The reaction mixture was stirred at ambient temperatureovernight. It was quenched with water and the mixture stirred foranother 15 min. The precipitated solid was collected by filtration,washed with water (3×) and dried to yield the desired product (4.8 g,1:1 mixture of regioisomers, 70% purity), which was used in the nextstep without further purification.

Regioisomer 1: LC-MS (method 9): Rt=1.03 min; MS (ESIpos): m/z=338[M+H]⁺

Regioisomer 2: LC-MS (method 9): Rt=1.09 min; MS (ESIpos): m/z=338[M+H]⁺

Intermediate 70 4-chloro-1-methyl-3-phenyl-1H-pyrazol-5-amine

2-(4-chloro-1-methyl-3-phenyl-1H-pyrazol-5-yl)-1H-isoindole-1,3(2H)-dione (4.80 g, 14.2 mmol) was dissolved in ethanol (120 mL) andtreated with hydrazine monohydrate (3.5 mL, 71 mmol). The reactionmixture was heated to reflux overnight. After cooling to ambienttemperature, the precipitated solid was removed by filtration and washedwith ethanol. The combined filtrates were purified by flash columnchromatography on silica gel (eluent: dichloromethane/methanol) andpreparative HPLC (column: Daicel Chiracel OJ-H 5 μM, 250×20 mm, flow 100mL/min, 80% carbon dioxide/20% methanol, 40° C., detection at 210 nM)for the separation of the two regioisomers. The desired product wasobtained as a white solid (431 mg, 15% yield).

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 3.309 (16.00), 4.846 (6.68), 7.443(3.94), 7.464 (6.84), 7.486 (2.33), 7.510 (4.29), 7.529 (4.30), 7.546(1.30).

Intermediate 71 4-chloro-1-methyl-5-phenyl-1H-pyrazol-3-amine

The desired product was obtained from the regioisomer separationdescribed for the synthesis of4-chloro-1-methyl-3-phenyl-1H-pyrazol-5-amine (576 mg, 20%).

LC-MS (method 10): R_(t)=1.39 min; MS (ESIpos): m/z=208 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: 0.007 (0.35), 1.038 (0.09), 1.055(0.20), 1.072 (0.10), 2.327 (0.11), 2.365 (0.08), 2.669 (0.12), 2.709(0.08), 3.434 (0.09), 3.611 (16.00), 3.783 (0.08), 5.494 (3.59), 7.295(0.47), 7.314 (1.45), 7.319 (0.47), 7.332 (1.11), 7.382 (1.99), 7.401(3.20), 7.415 (0.54), 7.420 (1.43), 7.760 (2.67), 7.778 (2.68), 7.781(1.97).

Intermediate 722-[5-(4-fluorophenyl)-4-methyl-1H-pyrazol-3-yl]-1H-isoindole-1,3(2H)-dione

5-(4-fluorophenyl)-4-methyl-1H-pyrazol-3-amine (1.50 g, 7.84 mmol) and2-benzofuran-1,3-dione (1.74 g, 11.8 mmol) were suspended in acetic acid(15 mL) and heated under reflux for 1 hour. After cooling to ambienttemperature, the solvent was removed under reduced pressure and theresidue re-dissolved in methyl t-butyl ether at 50° C. The remaininginsoluble solid was collected by filtration and washed further withmethyl t-butyl ether. The desired product was obtained, which was usedin the next step without further purification (2.2 g, 87% yield).

LC-MS (method 11): Rt=1.22 min; MS (ESIpos): m/z=322 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 1.908 (0.50), 1.996 (16.00), 2.327(0.20), 2.366 (0.15), 2.669 (0.22), 2.709 (0.17), 7.361 (1.84), 7.382(3.67), 7.404 (2.02), 7.565 (0.21), 7.573 (0.23), 7.579 (0.23), 7.587(0.30), 7.666 (2.60), 7.680 (3.21), 7.687 (3.04), 7.701 (2.42), 7.940(3.30), 7.948 (3.94), 7.954 (4.10), 7.962 (6.07), 7.972 (1.27), 7.993(1.11), 8.003 (5.18), 8.011 (3.63), 8.017 (3.44), 8.025 (2.75), 13.370(2.34).

Intermediate 732-[3-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione

2-[5-(4-fluorophenyl)-4-methyl-1H-pyrazol-3-yl]-1H-isoindole-1,3(2H)-dione(2.20 g, 6.85 mmol) and potassium carbonate were suspended in DMF (10mL). Methyl iodide (0.85 mL, 14 mmol) was added and the resultingreaction mixture was stirred at ambient temperature overnight. Thereaction was quenched by addition of water and extracted with ethylacetate (3×). The combined organic phases were dried over sodium sulfateand concentrated. The two produced regioisomers were separated by flashcolumn chromatography on silica gel (eluent:ethyl acetate/cyclohexane0:100 to 50:50 gradient). The desired product was isolated as a whitesolid (965 mg, 42% yield) separated from its regioisomer.

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 1.156 (0.32), 1.174 (0.67), 1.191(0.33), 1.396 (1.96), 1.987 (1.30), 2.017 (15.46), 3.735 (16.00), 4.019(0.31), 4.037 (0.29), 7.265 (1.96), 7.287 (4.06), 7.309 (2.15), 7.705(2.15), 7.711 (0.89), 7.719 (2.38), 7.727 (2.19), 7.736 (0.84), 7.742(1.96), 7.963 (2.25), 7.971 (2.46), 7.977 (2.43), 7.985 (3.72), 7.995(0.56), 8.030 (0.54), 8.040 (3.89), 8.047 (2.54), 8.053 (2.57), 8.061(2.24).

Intermediate 742-[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]-1H-isoindole-1,3(2H)-dione

The desired product was obtained from the regioisomer separationdescribed for2-[3-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(904 mg, 39% yield).

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 1.156 (0.26), 1.173 (0.53), 1.191(0.27), 1.656 (0.08), 1.817 (15.98), 1.976 (0.10), 1.987 (0.98), 2.017(0.09), 2.327 (0.08), 2.365 (0.06), 2.669 (0.09), 2.709 (0.06), 3.595(0.08), 3.735 (0.11), 3.773 (16.00), 3.947 (0.08), 4.001 (0.08), 4.019(0.24), 4.037 (0.23), 4.054 (0.08), 7.377 (1.84), 7.399 (3.98), 7.421(2.25), 7.574 (2.33), 7.579 (1.03), 7.587 (2.64), 7.595 (2.15), 7.609(1.84), 7.934 (2.16), 7.942 (2.49), 7.948 (2.57), 7.955 (3.92), 7.966(0.73), 7.987 (0.69), 7.998 (3.84), 8.006 (2.45), 8.012 (2.32), 8.020(1.95).

Intermediate 75 3-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-5-amine

2-[3-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(965 mg, 2.88 mmol) was dissolved in ethanol (24 mL) and hydrazinemonohydrate (0.70 mL, 14 mmol) was added at ambient temperature. Thereaction mixture was heated under reflux for 2 hours. After cooling toroom-temperature, the precipitated white solid was removed by filtrationand washed with ethanol. The combined filtrate was concentrated and theresidue purified by flash column chromatography on silica gel (eluent:dichlormethane/methanol 92:8) to yield 515 mg of the desired product(85% yield).

LC-MS (method 11): Rt=0.79 min; MS (ESIpos): m/z=206 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.009 (0.15), 0.007 (0.15), 1.234(0.05), 1.753 (0.07), 1.810 (0.08), 1.970 (15.83), 2.125 (0.08), 2.327(0.06), 2.366 (0.05), 2.669 (0.07), 2.709 (0.05), 3.377 (0.09), 3.439(0.07), 3.552 (16.00), 3.724 (0.08), 4.948 (3.84), 7.151 (0.19), 7.158(1.78), 7.163 (0.60), 7.175 (0.76), 7.181 (3.78), 7.186 (0.75), 7.198(0.65), 7.203 (2.07), 7.211 (0.24), 7.557 (0.22), 7.564 (2.01), 7.570(0.80), 7.578 (2.19), 7.586 (2.07), 7.595 (0.76), 7.600 (1.85), 7.608(0.21).

Intermediate 76 5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-amine

2-[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]-1H-isoindole-1,3(2H)-dione(904 mg, 2.70 mmol) was dissolved in ethanol (22.6 mL) and hydrazinemonohydrate (0.65 mL, 13.5 mmol) was added at ambient temperature. Thereaction mixture was heated under reflux for 2 hours. After cooling toroom-temperature, the precipitated white solid was removed by filtrationand washed with ethanol. The combined filtrate was concentrated and theresidue purified by flash column chromatography on silica gel (eluent:dichlormethane/methanol 92:8) to yield 451 mg of the desired product asa white solid (82% yield).

LC-MS (method 11): Rt=0.88 min; MS (ESIpos): m/z=206 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 1.753 (15.74), 2.669 (0.14), 3.439(16.00), 4.442 (3.93), 7.293 (1.45), 7.298 (0.57), 7.309 (0.86), 7.315(3.99), 7.321 (0.83), 7.332 (0.74), 7.337 (2.71), 7.372 (2.60), 7.378(0.97), 7.386 (2.85), 7.394 (1.76), 7.402 (0.65), 7.408 (1.41).

Intermediate 77 ethyl1-(6-chloropyrimidin-4-yl)-5-methyl-1H-pyrazole-3-carboxylate

A solution of 4-chloro-6-hydrazinylpyrimidine (2.00 g, 13.8 mmol) andethyl 2,4-dioxopentanoate (2.19 g, 13.8 mmol) in ethanol (40 ml) wasrefluxed overnight. After cooling to room temperature a precipitate wasformed which was filtered and dried to afford 2.25 g (61% yield) of thedesired product. The filtrate was processed further to yield theregioisomeric product.

LC-MS (method 11): Rt=1.33 min; MS (ESIpos): m/z=267 [M+H]⁺

¹H-NMR (600 MHz, DMSO-d₆): δ [ppm]: 1.32 (t, 4H), 4.34 (q, 3H), 6.88 (d,1H), 8.02 (d, 1H), 9.05 (d, 1H).

Intermediate 78 ethyl1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate

The filtrate out of the synthesis of ethyl1-(6-chloropyrimidin-4-yl)-5-methyl-1H-pyrazole-3-carboxylate wasconcentrated and purified by reparative HPLC (method: column: ReprosilC18; 10 μm; 125×30 mm/flow: 45 ml/min/eluent: A=water (0.1% formicacid), B=acetonitrile/gradiente: 0.00-4.25 min=10% B, 4.50 min=20% B,15.50 min=85% B, 16.00-18.50 min=100% B, 18.75-22.00 min=20% B) toafford the desired product (544mg, 15% yield).

LC-MS (method 11): R_(t)=1.28 min; MS (ESIpos): m/z=267 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 1.214 (4.65), 1.232 (9.58), 1.250(4.68), 1.304 (0.72), 1.322 (1.49), 1.340 (0.82), 2.289 (0.52), 2.316(16.00), 2.722 (2.13), 4.280 (1.61), 4.298 (4.62), 4.315 (4.72), 4.333(2.02), 4.349 (0.72), 6.883 (0.57), 6.914 (4.78), 7.985 (3.83), 8.026(0.61), 8.933 (3.80), 9.047 (0.60).

Intermediate 792-[4-chloro-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione

The described product was prepared in a manner analogous to thatdescribed in the preparation of2-[4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dionestarting from 4-chloro-3-(4-fluorophenyl)-1H-pyrazol-5-amine (1.14 g,5.39 mmol) and 2-benzofuran-1,3-dione (1.20 g, 8.08 mmol) to yield 2.0 gof the desired product [quant.].

LC-MS (method 10): R_(t)=1.86 min; MS (ESIpos): m/z=342 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.149 (0.52), −0.008 (4.13), 0.008(3.94), 0.146 (0.50), 1.910 (0.92), 2.074 (1.32), 2.329 (0.50), 2.368(0.52), 2.525 (1.57), 2.667 (0.40), 2.672 (0.54), 2.712 (0.52), 7.427(6.99), 7.449 (14.26), 7.471 (7.64), 7.571 (1.75), 7.579 (1.92), 7.585(1.83), 7.593 (2.62), 7.603 (0.41), 7.670 (1.29), 7.678 (1.19), 7.683(1.19), 7.691 (0.92), 7.848 (8.15), 7.862 (9.33), 7.870 (8.83), 7.883(7.57), 7.978 (8.99), 7.986 (10.59), 7.992 (11.17), 8.000 (16.00), 8.010(3.32), 8.021 (1.02), 8.038 (2.68), 8.048 (13.92), 8.056 (10.03), 8.062(9.64), 8.070 (8.09), 8.081 (1.45), 8.095 (0.54), 8.103 (0.48), 14.071(8.74).

Intermediate 802-[4-chloro-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-1H-isoindole-1,3(2H)-dione

The described product was prepared in a manner analogous to thatdescribed in the preparation of2-[4-ethyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione starting from2-[4-chloro-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(2.20 g, 6.44 mmol) and iodomethane (800 μl, 13 mmol) to yield 601 mg ofthe desired product (23% yield) after separation of the regioisomers(Instrument: THAR SFC-Super Chrom Prep 200, column: Chirapak AD-H (SFC)5 μm, 250×30 mm, eluent: carbon dioxide/methanol 76:24, pressure: 135bar, temperature eluent: 38° C., temperatur Zyklon: 40° C., pressureZyklon 24 bar, flow: 108 g/min, UV 210 nm).

LC-MS (method 10): R_(t)=1.99 min; MS (ESIpos): m/z=356 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 3.764 (0.61), 3.784 (1.31), 3.873(16.00), 7.434 (2.11), 7.456 (4.30), 7.478 (2.35), 7.688 (2.38), 7.693(1.22), 7.701 (2.60), 7.710 (2.33), 7.718 (0.97), 7.723 (1.99), 7.973(2.24), 7.981 (2.53), 7.987 (2.62), 7.995 (3.88), 8.005 (0.67), 8.035(0.65), 8.045 (3.91), 8.053 (2.60), 8.059 (2.63), 8.066 (2.23).

Intermediate 812-[4-chloro-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione

The desired product was obtained out of the separation of theregiosiomers in the preparation of2-[4-chloro-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-1H-isoindole-1,3(2H)-dione(789 mg, 34%).

LC-MS (method 10): Rt=2.14 min; MS (ESIpos): m/z=357 [M+H]⁺

¹H-NMR (500 MHz, DMSO-d₆): δ [ppm]: 3.87 (s, 3H), 7.28-7.40 (m, 2H),7.86-7.93 (m, 2H), 7.98-8.04 (m, 2H), 8.07-8.14 (m, 2H).

Intermediate 82 4-chloro-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation of4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine starting from2-[4-chloro-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-1H-isoindole-1,3(2H)-dione(600 mg, 1.69 mmol) and hydrazine hydrate (1:1) (410 μl, 8.4 mmol) toyield 370 mg of the desired product (97% yield) after cyrstallisationfrom acetonitrile.

¹H-NMR (400 MHz, DMSO-d₆): δ [ppm]: 3.52 (s, 3H), 4.86 (s, 2H),7.32-7.42 (m, 2H), 7.48-7.56 (m, 2H).

Intermediate 83 4-chloro-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation of4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine starting from2-[4-chloro-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(790 mg, 2.22 mmol) to yield 490 mg of the desired product (96% yield)after cyrstallisation from acetonitrile.

¹H-NMR (400 MHz, DMSO-d6): δ [ppm]: 3.60 (s, 3H), 5.52 (s, 2H),7.17-7.32 (m, 2H), 7.72-7.91 (m, 2H).

Intermediate 84 ethyl1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate

The described product was prepared in a manner analogous to thatdescribed in the preparation ofN-[4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3-methyl-1H-indazol-1-yl)pyrimidin-4-aminestarting from 4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine(100 mg, 456 μmol) and ethyl1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate (122 mg,456 μmol) to yield the desired product 106 mg (52% yield).

LC-MS (method 11): R_(t)=1.43 min; MS (ESIpos): m/z=450 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: −0.008 (0.67), 0.008 (0.46), 0.877(3.86), 0.896 (8.85), 0.914 (3.98), 1.074 (0.65), 1.091 (1.28), 1.109(0.65), 1.196 (5.36), 1.214 (11.31), 1.231 (5.47), 2.272 (16.00), 2.299(0.98), 2.318 (2.72), 2.336 (2.64), 2.355 (0.85), 3.314 (7.67), 3.375(0.66), 3.392 (0.63), 4.239 (1.72), 4.257 (5.40), 4.275 (5.33), 4.293(1.66), 6.750 (5.30), 7.256 (1.59), 7.358 (2.08), 7.363 (0.78), 7.380(4.69), 7.402 (2.78), 7.506 (2.79), 7.511 (1.21), 7.519 (3.13), 7.527(2.45), 7.536 (1.02), 7.541 (2.07), 8.413 (3.12), 9.581 (1.76).

Intermediate 85 Sodium (2E)-3-cyano-4-oxopent-2-en-2-olate

1-(5-methyl-1,2-oxazol-4-yl)ethanone (1000 mg, 7.99 mmol, CAS 6497-21-8)was dissolved in ethanol and the mixture was added to an ethanolicsolution of sodium hydroxide (320 mg, 7.99 mmol) which was cooled in dryice. The white powder that precipitates was filtered and washed withethanol. The crude product was used as such in the next step 995 mg (84%yield).

Intermediate 86 3,5-dimethyl-1H-pyrazole-4-carbonitrile

A mixture of sodium (2E)-3-cyano-4-oxopent-2-en-2-olate (995 mg, 6.78mmol) and hydrazine hydrate (1:1) (390 _(j)ul, 8.0 mmol) in water (10mL) was refluxed overnight. After cooling to room temperature thereaction mixture was concentrated under vacuum to afford 1.03 g (quant.)of the desired product which was used as such in the next step.

LC-MS (method 11): R_(t)=0.58 min; MS (ESIpos): m/z=122 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 1.609 (0.43), 2.041 (0.70), 2.084(16.00), 2.242 (3.61), 3.473 (0.45).

Intermediate 871-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbonitrile

4,6-dichloropyrimidine (1.27 g, 8.50 mmol),3,5-dimethyl-1H-pyrazole-4-carbonitrile (1.03 g, 8.50 mmol) and caesiumcarbonate were dissolved in DMF. The reaction mixture was stirred atroom temperature overnight. Water was added and the resulting mixturewas stirred at room temperature for 30 min. The precipitate wasfiltered, washed with water and dried under reduced pressure to affordthe desired product 1.06 g (53% yield), which was used as such in thenext step.

LC-MS (method 11): R_(t)=1.28 min; MS (ESIpos): m/z=234 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 2.339 (0.76), 2.378 (15.68), 2.403(1.58), 2.732 (0.44), 2.781 (0.70), 2.826 (16.00), 2.868 (1.38), 2.891(0.55), 5.754 (0.68), 8.014 (2.62), 9.038 (2.54).

Intermediate 882-[1-(2-{[tert-butyl(dimethyl)silyl]oxy}ethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione

A solution of2-[4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(1.27 g, 3.80 mmol) and (2-bromoethoxy)(tert-butyl)dimethylsilane (1.6ml, 7.6 mmol) in DMF (7.0 ml) was treated with potassium carbonate (1.05g, 7.60 mmol) and stirred at room temperature of 4 days. The mixture wasdiluted with water and ethyl acetate. The aqueous layer was extractedtwice with ethyl acetate. The organic phases were gathered, dried oversodium sulfate and concentrated under vacuum. he crude product waspurified by column chromatography on silica gel using cyclohexane/ethylacetate to afford two region isomers. The desired product was obtainedin 31% yield (575 mg).

LC-MS (method 11): R_(t)=1.80 min; MS (ESIpos): m/z=494 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: −0.221 (0.06), −0.071 (11.32), −0.042(0.17), −0.006 (1.77), 0.041 (0.14), 0.076 (0.05), 0.617 (0.08), 0.774(16.00), 0.790 (2.87), 0.809 (1.41), 0.848 (0.21), 0.929 (0.08), 1.049(0.03), 1.151 (0.07), 1.168 (0.14), 1.186 (0.07), 1.982 (0.25), 2.187(0.38), 2.206 (1.07), 2.225 (1.03), 2.244 (0.32), 2.322 (0.03), 2.362(0.03), 2.665 (0.03), 3.896 (0.61), 3.909 (1.30), 3.922 (0.74), 4.014(0.09), 4.045 (0.81), 4.058 (1.25), 4.071 (0.53), 7.365 (0.61), 7.387(1.29), 7.409 (0.72), 7.566 (0.83), 7.580 (0.95), 7.588 (0.79), 7.602(0.63), 7.937 (0.80), 7.945 (0.91), 7.951 (0.94), 7.959 (1.26), 7.969(0.25), 7.997 (0.29), 8.007 (1.31), 8.015 (0.90), 8.020 (0.82), 8.028(0.68).

Intermediate 891-(2-{[tert-butyl(dimethyl)silyl]oxy}ethyl)-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-amine

2-[1-(2-{[tert-butyl(dimethyl)silyl]oxy}ethyl)-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]-1H-isoindole-1,3(2H)-dione(875 mg, 1.77 mmol) was dissolved in ethanol and treated with hydrazinehydrate (1:1) (430 μl, 8.9 mmol). The reaction mixture was stirred at90° C. for 2 hours. The reaction mixture was cooled and filtered. Thefiltrate was concentrated under vacuum and was used as such in the nextstep.

LC-MS (method 11): R_(t)=1.58 min; MS (ESIpos): m/z=364 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.096 (0.56), −0.089 (12.22), −0.081(0.57), 0.774 (16.00), 0.889 (0.98), 0.907 (2.34), 0.926 (1.05), 2.169(0.91), 2.188 (0.88), 3.724 (0.93), 3.736 (0.74), 3.771 (0.76), 3.783(0.97), 4.480 (0.88), 7.280 (0.50), 7.302 (1.24), 7.325 (0.77), 7.386(0.79), 7.400 (0.88), 7.408 (0.63), 7.422 (0.52).

Intermediate 90N-[1-(2-{[tert-butyl(dimethypsilyl]oxy}ethyl)-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A flame-dried three-necked round-bottom flask equipped with a refluxcondenser was charged with 1,4-dimethyl-1H-pyrazol-3-amine (347 mg, 1.5mmol),1-(2-{[tert-butyl(dimethyl)silyl]oxy}ethyl)-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-amine(551 mg, 1.5 mmol) and sodium phenoxide (264 mg, 2.3 mmol). The solidswere suspended in dry 1,4-dioxane (10 mL) and the mixture was degassedby bubbling Argon through the solution for 3 min.Tris(dibenzylidenacetone)dipalladium (27 mg, 30 μmol) and XantPhos (43mg, 78 μmol) were added and the mixture again degassed for 1 min. Thereaction mixture was heated at 85° C. for 16 hours. After cooling toambient temperature, the mixture was purified by preparative HPLC(method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 45 ml/min/eluent:A=water (0.1% formic acid), B=acetonitrile/gradient: 0.00-4.25 min=20%B, 4.50 min=70% B, 15.50 min=85% B, 16.00-23.00 min=100% B, 23.00-27.00min=20% B) to afford the desired product (250 mg, 31% yield).

LC-MS (method 10): R_(t)=2.99 min; MS (ESIpos): m/z=536 [M+H]⁺

Intermediate 91N-(1,4-dimethyl-1H-pyrazol-3-yl)-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-aminetrifluoroacetate

A flame-dried three-necked round-bottom flask equipped with a refluxcondenser was charged with 1,4-dimethyl-1H-pyrazol-3-amine (1.00 g, 9.00mmol), 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (2.06 g, 9.90mmol) and sodium phenoxide (1.57 g, 13.5 mmol). The solids weresuspended in dry 1,4-dioxane (18 mL) and the mixture was degassed bybubbling Argon through the solution for 3 min.Tris(dibenzylidenacetone)dipalladium (124 mg, 135 μmol) and XantPhos(156 mg, 270 μmol) were added and the mixture again degassed for 1 min.The reaction mixture was heated at 80° C. for 16 hours. After cooling toambient temperature, the mixture was diluted with ethyl acetate andfiltered through Celite. The combined washings were concentrated and theresidue purified by preparative HPLC (column: Chromatorex C18; 250*40mm, 10 μM, flow 100 mL/min, gradient acetonitrile/water (containing 0.1%trifluoroacetic acid) 90/10 to 5/95) to yield the desired product as itstrifluoroacetate salt (1.05 g, 29% yield).

LC-MS (method 11): R_(t)=1.07 min; MS (ESIpos): m/z=284 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: −0.008 (1.26), 0.008 (0.69), 1.878(12.45), 2.073 (0.47), 2.169 (14.25), 2.519 (0.73), 2.524 (0.65), 2.609(12.08), 3.688 (0.42), 3.751 (16.00), 6.117 (3.23), 7.171 (3.60), 7.484(3.07), 8.415 (3.31), 9.254 (2.53).

Intermediate 922-methyl-3-oxo-3-[4-(trifluoromethoxy)phenyl]propanenitrile

Methyl 4-(trifluoromethoxy)benzoate (5.00 g, 22.7 mmol) andpropanenitrile (2.4 mL, 34 mmol) were dissolved in THF and cooled with awater bath to 20° C. Lithium 1,1,1,3,3,3-hexamethyldisilazan-2-ide (1.0M, 35 mL, 35 mmol) was added slowly and the reaction mixture stirred atambient temperature for 2 h. The reaction mixture was quenched by theaddition of water and extracted with ethyl acetate (3×). The combinedorganic extracts were dried over magnesium sulfate and concentrated. Theresidue obtained was used in the next step without further purification(4.00 g, 55% yield, 76% purity).

Intermediate 934-methyl-3-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-5-amine

2-methyl-3-oxo-3[4-(trifluoromethoxy)phenyl]propanenitrile (4.00 g, 16.4mmol, 76% purity) was dissolved in ethanol and hydrazine monohydrate(1.6 mL, 33 mmol) was added dropwise via a syringe. The reaction mixturewas heated under reflux overnight. All volatiles were removed underreduced pressure and the residue purified by preparative HPLC (column:Chromatorex C18; 250*40 mm, 10 μM, flow 100 mL/min, gradientacetonitrile/water (containing 0.1% trifluoroacetic acid) 90/10 to 5/95)to yield the desired product as a yellow solid (3.0 g, 80% purity, 56%yield).

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.015 (0.51), 1.278 (0.11), 1.297(0.24), 1.316 (0.12), 1.885 (0.08), 2.047 (16.00), 2.205 (0.08), 2.322(0.09), 2.361 (0.09), 2.664 (0.10), 2.705 (0.09), 2.798 (0.11), 2.817(0.11), 7.508 (2.65), 7.530 (3.25), 7.693 (0.66), 7.700 (5.14), 7.705(1.55), 7.717 (1.49), 7.722 (4.07), 7.729 (0.46), 7.970 (0.37), 7.977(2.89), 7.982 (0.90), 7.994 (0.92), 7.999 (2.59), 8.141 (0.13), 8.163(0.13), 11.057 (0.09).

Intermediate 942-{4-methyl-3-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-5-yl}-1H-isoindole-1,3(2H)-dione

4-methyl-3-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-5-amine (2.00 g, 7.78mmol) and 2-benzofuran-1,3-dione (1.73 g, 11.7 mmol) were suspended inacetic acid (15 mL) and heated under reflux. After 30 min of heating,all solids were completely dissolved. The reaction mixture was stirredunder reflux overnight until full conversion of starting material. Aftercooling to ambient temperature, the mixture was concentrated underreduced pressure and co-evaporated with methanol (3×). The residue thusobtained was used in the next step without further purification.(3.0 g,99% yield)

LC-MS (method 10): Rt=2.00 min; MS (ESIpos): m/z=388 [M+H]⁺

Intermediate 952-{1,4-dimethyl-5-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-3-yl}-1H-isoindole-1,3(2H)-dione

2-{4-methyl-3-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-5-yl}-1H-isoindole-1,3(2H)-dione(3.00 g, 7.75 mmol) and potassium carbonate (2.14 g, 15.5 mmol) weresuspended in DMF (11 mL), when iodomethane (960 μL, 15 mmol) was addeddropwise. The reaction mixture was stirred at ambient temperatureovernight. It was quenched by addition of water and extraxted with ethylacetate (3×). The combined organic extracts were dried over sodiumsulfate and concentrated. The residue was purified by flash columnchromatography on silica gel (cyclohexane/etyhl acetate gradient) toyield the desired product together with its regioisomer as a mixture(˜1:1) as a yellow solid (2.0 g, 64%).

LC-MS (method 10): Rt=2.15 min; MS (ESIpos): m/z=402 [M+H]⁺

Intermediate 961,4-dimethyl-5-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-3-amine

The mixture of2-{1,4-dimethyl-5-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-3-yl}-1H-isoindole-1,3(2H)-dioneand its regioisomer (2.00 g, 4.98 mmol) was dissolved in ethanol (43 mL)and hydrazine monohydrate was added (1.2 mL, 25 mmol). The reactionmixture was heated under reflux overnight. After cooling to ambienttemperature, all volatiles were removed under reduced pressure and theresidue was purified by preparative HPLC (column: Daicel Chiralpak IF250×20 mm, 5 μm, Flow: 15 mL/min, T=35° C., eluent: n-heptane/ethanol75:25) to yield the desired product (329 mg, 24% yield) as a singleisomer along with its regioisomer (see Intermediate 106).

LC-MS (method 10): Rt=1.57 min; MS (ESIpos): m/z=272 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]:) 1.77 (s, 3H), 2.86 (s, 3H), 4.48 (s,2H), 7.46-7.52 (m, 4H).

Intermediate 971-(cyclopropylmethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-amine

2-(4-fluorobenzoyl)butanenitrile (300 mg, 1.57 mmol) was dissolved in2-propanol (10 ml). Then, (cyclopropylmethyl)hydrazine dihydrochloride(299 mg, 1.88 mmol) was added and the reaction mixture was stirred atreflux overnight. After cooling to room temperature a 1 M solution ofsodium hydrogencarbonate was added and the reaction mixture wasconcentrated in vacuum. The crude product was purified by preparativeHPLC (method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 45ml/min/eluent: A=water (0,1% formic acid), B=acetonitrile /gradient:0.00-4.25 min=10% B, 4.50 min=20% B, 15.50 min=85% B, 16.00-18.50min=100% B, 18.75-22.00 min=20% B) to afford 154 mg (38% yield).

LC-MS (method 11): R_(t)=1.08 min; MS (ESIpos): m/z=261 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.31-0.49 (m, 4H), 1.00 (t, 3H),1.13-1.29 (m, 1H), 2.43 (q, 2H), 3.79 (d, 2H), 4.90 (s, 2H), 7.11-7.26(m, 2H), 7.47-7.65 (m, 2H).

Intermediate 981-cyclopropyl-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-amine

2-(4-fluorobenzoyl)butanenitrile (300 mg, 1.57 mmol) was dissolved in2-propanol (10 ml). Then, cyclopropylhydrazine dihydrochloride (273 mg,1.88 mmol) was added and the reaction mixture was stirred at refluxovernight. After cooling to room temeparture a 1 M solution of sodiumhydrogencarbonate was added and the reaction mixture was concentrated invacuum. The crude product was purified by preparative HPLC (methode:column: Reprosil C18; 10 μm; 125×30 mm/flow: 45 ml/min/eluent: A=water(0,1% formic acid), B=acetonitrile/gradient: 0.00-4.25 min=10% B, 4.50min=20% B, 15.50 min=85% B, 16.00-18.50 min=100% B, 18.75-22.00 min=20%B) to afford 209 mg (54% yield).

LC-MS (method 11): R_(t)=0.96 min; MS (ESIpos): m/z=247 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (0.84), 0.008 (0.73), 0.888(1.03), 0.904 (3.46), 0.909 (3.52), 0.920 (4.25), 0.927 (3.61), 0.935(3.47), 0.951 (2.66), 0.962 (6.82), 0.972 (9.67), 0.981 (2.34), 0.990(16.00), 1.009 (6.89), 2.387 (1.94), 2.405 (6.08), 2.424 (5.97), 2.443(1.86), 3.251 (1.03), 3.261 (1.76), 3.269 (2.27), 3.279 (2.75), 3.283(1.88), 3.288 (1.88), 3.296 (1.77), 3.306 (1.09), 5.017 (4.79), 7.149(0.46), 7.157 (3.96), 7.162 (1.43), 7.174 (1.85), 7.179 (8.35), 7.185(1.84), 7.197 (1.53), 7.202 (4.61), 7.209 (0.55), 7.498 (0.60), 7.506(4.61), 7.511 (1.88), 7.519 (5.10), 7.527 (4.66), 7.536 (1.79), 7.541(4.12), 7.549 (0.54), 8.182 (0.93).

Intermediate 991-(cyclopropylmethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-amine

2-(4-fluorobenzoyl)butanenitrile (300 mg, 1.57 mmol) was dissolved in2-propanol (10 ml). Then, (cyclopropylmethyl)hydrazine dihydrochloride(299 mg, 1.88 mmol) was added and the reaction mixture was stirred atreflux overnight. A 1 M solution of sodium hydrogencarbonate was addedand the reaction mixture was concentrated in vacuum. The crude productwas purified by preparative HPLC (method: column: Reprosil C18; 10 μm;125×30 mm/flow: 45 ml/min/eluent: A=water (0.1% formic acid),B=acetonitrile/gradient: 0.00-4.25 min=10% B, 4.50 min=20% B, 15.50min=85% B, 16.00-18.50 min=100% B, 18.75-22.00 min=20% B) to afford 154mg (38% yield) as desired product.

LC-MS (method 11): R_(t)=1.06 min; MS (ESIpos): m/z=261.2 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.29-0.50 (m, 4H), 1.00 (t, 3H),1.14-1.28 (m, 1H), 2.43 (q, 2H), 3.79 (d, 2H), 4.90 (s, 2H), 7.13-7.24(m, 2H), 7.51-7.61 (m, 2H).

Intermediate 1002-[4-chloro-1-(2,2-difluoroethyl)-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione

A solution of2-[4-chloro-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(3.00 g, 8.78 mmol) in DMF (30 ml) was treated with 2,2-difluoroethyltrifluoromethanesulfonate (1.3 ml, 9.7 mmol) and (5.72 g, 17.6 mmol).The reaction mixture was stirred at room temperature for 1 h. Thereaction mixture was treated with water. Ethyl acetate was added and thewater layer was extracted twice. The organic phase was washed withbrine, dried over magnesium sulfate and concentrated under vacuum. Thecrude product was purified by column flash chromatography(cyclohexane/ethyl acetate) to afford two fractions corresponding to thetwo regioisomers of the desired product. The desired one was obtained in20% yield (709 mg).

LC-MS (method 11): Rt=1.47 min; MS (ESIpos): m/z=406 [M+H]⁺

Intermediate 1012-[4-chloro-1-(2,2-difluoroethyl)-5-(4-fluorophenyl)-1H-pyrazol-3-yl]-1H-isoindole-1,3(2H)-dione

A solution of2-[4-chloro-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(3.00 g, 8.78 mmol) in DMF (30 ml) was treated with 2,2-difluoroethyltrifluoromethanesulfonate (1.3 ml, 9.7 mmol) and (5.72 g, 17.6 mmol).The reaction mixture was stirred at room temperature for 1 h. LC/MSshowed no more starting material. The reaction mixture was quenched withwater. Ethyl acetate was added and the water layer was extracted twice.The organic phase was washed with brine, dried over magnesium sulfateand concentrated under vacuum. The crude product was purified by columnflash chromatography (cyclohexane/ethyl acetate) to afford two fractionscorresponding to the two regioisomers of the desired product. Thedesired regiosimere was obtained in 12% yield (427 mg).

LC-MS (method 11): R_(t)=1.40 min; MS (ESIpos): m/z=406 [m+H]⁺

Intermediate 1024-chloro-1-(2,2-difluoroethyl)-3-(4-fluorophenyl)-1H-pyrazol-5-amine

2-[4-chloro-1-(2,2-difluoroethyl)-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione (709 mg, 17.5 mmol) was dissolved in ethanol (5 mL) andtreated with hydrazine hydrate (0.42 mL, 8.7 mmol). The reaction mixturewas stirred at 80° C. for 1 h. The reaction mixture was cooled andfiltered. The filtrate was concentrated under vacuum. The crude productwas purified by preparative HPLC (method: column: Reprosil C18; 10 μm;125×30 mm/flow: 45 ml/min/eluent: A=water (0.1% formic acid),B=acetonitrile/gradient: 0.00-4.25 min=20% B, 4.50 min=70% B, 15.50min=85% B, 16.00-23.00 min=100% B, 23.00-27.00 min=20% B) to afford 79.2mg as desired product (16%).

LC-MS (method 11): R_(t)=1.21 min; MS (ESIneg): m/z=274 [M−H]⁻

Intermediate 1034-chloro-1-(2,2-difluoroethyl)-5-(4-fluorophenyl)-1H-pyrazol-3-amine

2-[4-chloro-1-(2,2-difluoroethyl)-5-(4-fluorophenyl)-1H-pyrazol-3-yl]-1H-isoindole-1,3(2H)-dione(427 mg, 1.05 mmol) was dissolved in ethanol (5.0 ml) and treated withhydrazine hydrate (1:1) (260 μl, 5.3 mmol). The reaction mixture wasstirred at 80° C. for 1 h. The reaction mixture was cooled and filtered.The filtrate was concentrated under vacuum. The crude product waspurified by preparative HPLC (method: column: Reprosil C18; 10 μm;125×30 mm/flow: 45 ml/min/eluent: A=water (0.1% formic acid),B=acetonitrile/gradient: 0.00-4.25 min=20% B, 4.50 min=70% B, 15.50min=85% B, 16.00-23.00 min=100% B, 23.00-27.00 min=20% B) to afford 193mg (67% yield) of the desird product.

LC-MS (method 11): R_(t)=1.16 min; MS (ESIpos): m/z=277 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 4.18 (td, 2H), 5.11 (s, 2H),6.03-6.39 (m, 1H), 7.34-7.42 (m, 2H), 7.43-7.53 (m, 2H).

Intermediate 104 2-(4-fluoro-2-methylbenzoyl)butanenitrile

Methyl 4-fluoro-2-methylbenzoate (2.00 g, 11.9 mmol) and butanenitrile(3.1 ml, 36 mmol) are placed in a flask placed under argon and weredissolved in THF (30 ml, 370 mmol). The solution was cooled with a waterbath to keep the reaction at room temperature. To this solution lithium1,1,1,3,3,3-hexamethyldisilazan-2-ide (37 ml, 1.0 M, 37 mmol) was slowlyadded over 10 minutes. Water and ethyl acetate were added, the mixturewas subsequently stirred for 10 minutes and acidicfied with aqueoushydrochloric acid. The mixture was three times extracted with ethylacetate, the combined organic phases were dried over sodium sulfate andconcentrated. The crude product (quant.) was used without any furtherpurification in the next step.

LC-MS (method 9): Rt=1.25 min; MS (ESIpos): m/z=206 [M+H]⁺

Intermediate 105 4-ethyl-5-(4-fluoro-2-methylphenyl)-1H-pyrazol-3-amine

2-(4-fluoro-2-methylbenzoyl)butanenitrile (2.50 g, 12.2 mmol) weredissolved in ethanol (13 ml, 220 mmol), hydrazine (1.5 ml, 64% purity,30 mmol) was added via syringe. The mixture was heated overnight at 95°C. bath temperature. After cooling to room temperature the reactionmixture was diluted with saturated sodium hydrogencarbonate solution andextracted two times with ethyl acetate. The combined organic phases weredried over magnesium sulfate and concentrated. The crude product waspurified b flash chromatography von silica gel(dichloromethane/methanol) to yield the desired prouct (quant.).

LC-MS (method 9): Rt=0.90 min; MS (ESIpos): m/z=221 [M+H]+

Intermediate 1061,4-dimethyl-3-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-5-amine

This compound was obtained during the separation of regioisomers asdescribed above for1,4-dimethyl-5-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-3-amine bypreparative HPLC (column: Daicel Chiralpak IF 250×20 mm, 5 μm, Flow: 15mL/min, T=35° C., eluent: n-heptane/ethanol 75:25) (single isomer, 467mg, 34% yield).

LC-MS (method 10): R_(t)=1.54 min; MS (ESIpos): m/z=272 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 2.00 (s, 3H), 3.57 (s, 3H), 4.99 (brs, 2H), 7.35 (d, J=8.2 Hz, 2H), 7.66-7.71 (m, 2H).

Intermediate 107 3-methyl-1,5,6,7-tetrahydro-4H-indazol-4-one

2-Acetylcyclohexane-1,3-dione (1.30 g, 8.43 mmol), hydrazine monohydrate(2.1 ml, 42 mmol) and p-toluenesulfonic acid monohydrate (80.2 mg, 422μmol) were suspended in ethanol (70 mL) and the reaction mixture washeated to reflux overnight. After cooling to ambient temperature, it wasdiluted with tetrahydrofuran (65 mL) and aqueous hydrochloric acid (2 M,75 mL) and vigorously stirred for further 5 h. All organic phasesolvents were removed under reduced pressure and the residual aqueousphase was extracted with ethyl acetate. The aqueous phase was basicifiedwith aqueous sodium hydroxide solution and extracted with ethyl acetate.The combined organic phase extracts were dried over sodium sulfate andconcentrated to yield the desired product (1.16 g, 89% yield) that wasused in the next step without further purification.

LC-MS (method 11): R_(t)=0.42 min; MS (ESIpos): m/z=151 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.55), −0.008(4.91), 0.008 (4.60), 0.146 (0.56), 1.175 (0.57), 1.908 (1.40), 1.970(5.21), 1.988 (6.92), 2.006 (5.54), 2.021 (3.61), 2.286 (16.00), 2.315(9.86), 2.329 (13.89), 2.344 (8.13), 2.367 (1.52), 2.396 (15.12), 2.524(1.38), 2.669 (3.83), 2.681 (5.70), 2.696 (3.71), 2.764 (3.98), 2.778(5.96), 2.792 (3.40), 12.741 (1.73), 12.888 (1.29).

Intermediate 1081-(6-chloropyrimidin-4-yl)-3-methyl-1,5,6,7-tetrahydro-4H-indazol-4-one

4,6-Dichloropyrimidine (1.15 g, 7.71 mmol),3-methyl-1,5,6,7-tetrahydro-4H-indazol-4-one (1.16 g, 7.71 mmol) andcesium carbonate (2.51 g, 7.71 mmol) were dissolved in dimethylformamide(55 mL) and stirred at ambient temperature overnight. Water was thenadded to cause precipitation of a white solid. After 5 minutes furtherstirring, the precipitated solid was collected by filtration and driedin an oven at 40° C. overnight to yield the desired product (1.34 g, 58%yield).

LC-MS (method 9): R_(t)=0.90 min; MS (ESIpos): m/z=263 [M+H]⁺

Intermediate 109 4-(2-cyanopropanoyl)benzonitrile

Ethyl 4-cyanobenzoate (10.0 g, 57.1 mmol) and propiononitrile (8.1 ml,110 mmol) were dissolved in tetrahydrofuran (170 mL) andbis-(trimethylsilyl)lithiumamide (1.0 m in tetrahydrofuran, 120 mL, 120mmol) was added to this solution dropwise at ambient temperature. Thereaction mixture was allowed to stir overnight. The reaction mixture wasquenched by addition of water and extracted with dichloromethane. Theorganic phase was discarded. The product-containing aqueous phase wasacidified with aqueous hydrochloric acid solution (6 M) and extractedwith dichloromethane (2×). The combined organic phase extracts werewashed with water, dried over sodium sulfate and concentrated. Theresidue was resuspended in diethylether and vigorously stirred. Theremaining solid was filtered, washed with diethylether and dried. Theproduct (7.83 g, 75% yield) was used in the next step without furtherpurification.

LC-MS (method 9): R_(t)=0.70 min; MS (ESIneg): m/z=183 [M−H]⁻

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.473 (3.09), 1.491(3.18), 1.669 (2.16), 1.892 (16.00), 5.178 (0.78), 5.196 (0.77), 7.616(0.53), 7.637 (0.59), 7.736 (3.94), 7.757 (4.82), 7.950 (4.87), 7.971(4.05), 8.047 (0.42), 8.073 (1.09), 8.094 (1.90), 8.155 (2.02), 8.176(1.19), 11.149 (1.39).

Intermediate 110 4-(3-amino-4-methyl-1H-pyrazol-5-yl)benzonitrile

4-(2-cyanopropanoyl)benzonitrile (7.00 g, 38.0 mmol) was dissolved inethanol (85 mL) and hydrazine monohydrate (2.4 ml, 49 mmol) was added atambient temperature. The reaction mixture was heated to reflux andstirred for 3 h. After cooling to ambient temperature, the reactionmixture was quenched with aqueous sodium hydrogencarbonate solution (1M, 50 mL). All volatiles were removed by rotary evaporation causing ayellow solid to precipitate. The solid was filtered, washed with waterand dried under vacuum to yield the desired product (6.8 g, 90% yield)

LC-MS (method 10): R_(t)=1.09 min; MS (ESIpos): m/z=199 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.02 (s, 3H) 4.68 (s,2H) 7.75 (d, J=8.44 Hz, 2H) 7.87 (d, J=8.44 Hz, 2H) 11.50-12.16 (br s,1H).

Intermediate 1114-chloro-6-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine

4-Chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (1.00g, 4.09 mmol) was dissolved in acetonitrile (20 mL) and treated withN-chlorosuccinimide (655 mg, 4.91 mmol) at ambient temperature. Thereaction mixture was stirred overnight. As LC-MS did not show fullconversion, a second aliquot of N-chlorosuccinimide (700 mg, 5.24 mmol)was added and the reaction mixture allowed to stir overnight. Water (75mL) was added to cause precipitation of a beige solid that was filtered,washed with water and dried under vacuum to yield the desired product(975 mg, 78% yield).

LC-MS (method 10): R_(t)=2.19 min; MS (ESIpos): m/z=279 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.327 (16.00), 7.817(1.38), 7.947 (2.75), 8.015 (2.73), 8.078 (1.33), 9.001 (2.65).

Intermediate 1124-[5-amino-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile

4-(2-cyanopropanoyl)benzonitrile (35.0 g, 190 mmol) was dissolved in2-propanol (500 mL) and the reaction mixture was heated to 80° C. Asolution of (cyclopropylmethyl)hydrazine dihydrochloride (2 in ethanol,103 mL, 206 mmol) was added dropwise and the reaction mixture wasallowed stir at reflux for 3 days. After cooling to 0° C., theprecipitated solid was filtered and discarded, the filtrate wasconcentrated (but not to dryness). It was diluted with water andbasicified with solid sodium hydrogencarbonate to pH 7-8. This mixturewas extracted with methyl tert-butylether (3×). The combined organicphase extracts were dried over magnesium sulfate and concentrated. Theresidue was purified by flash column chromatography (750 g silica gel,gradient cychlohexane/ethyl acetate 80/20 to 50/50) to yield the desiredproduct (29.6 g, 61% yield).

LC-MS (method 10): R_(t)=1.47 min; MS (ESIpos): m/z=253 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (1.21), 0.354(3.82), 0.365 (4.26), 0.402 (0.40), 0.431 (3.12), 0.451 (3.41), 1.184(0.44), 1.199 (0.92), 1.214 (1.17), 1.231 (0.88), 2.033 (15.49), 2.034(15.43), 3.824 (5.03), 3.841 (4.95), 5.022 (6.26), 7.778 (1.20), 7.798(16.00), 7.821 (1.09).

Intermediate 113 tert-butyl (2Z)-3-(methylamino)but-2-enoate (10:1mixture with (2E)-Isomer)

To a suspension of tert-butyl 3-oxobutanoate (17 ml, 100 mmol) andsilica gel (1.05 g) was added an aqueous solution of methylamine (40%,10 mL, 120 mmol). The reaction mixture was stirred overnight at ambienttemperature. GC-MS showed full conversion to product. Brine was addedand the reaction mixture was extracted with dichloromethane (3×). Thecombined organic phase extracts were dried over sodium sulfate,concentrated and dried to yield the desired product (16.9 g, 99% yield)as a 10:1 mixture of olefin isomers. The product was used in the nextstep without further purification.

GC-MS (method 15): R_(t)=3.61 min; MS (EI): m/z=171 [M].

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.371 (16.00), 1.837(4.88), 2.122 (0.45), 2.819 (2.83), 2.833 (2.81), 4.260 (1.34).

Intermediate 114 tert-butyl(2Z)-2-(difluoroacetyl)-3-(methylamino)but-2-enoate (10:1 mixture with(2E)-Isomer)

Tert-butyl (2Z)-3-(methylamino)but-2-enoate (16.8 g, 98.1 mmol, 10:1mixture with (2E)-Isomer) and triethylamine (21 ml, 150 mmol) weredissolved in methyl tert-butylether (190 mL) under an argon atmosphereand the resulting solution cooled to 0° C. Difluoroacetic anhydride (15ml, 120 mmol) was added dropwise and the reaction mixture allowed towarm to ambient temperature and was stirred overnight. The reactionmixture was diluted with methyl tert-butylether and washed with water(3×20 mL). The organic phase was dried over sodium sulfate andconcentrated. The residue was titurated with hexanes to yield thedesired product as a white solid (20.0g, 82% yield, 10:1 olefinisomers).

LC-MS (method 10): R_(t)=1.70 min; MS (ESIneg): m/z=248 [M−H]⁻

¹H-NMR (400 MHz, dimethylsulfoxide-d6, only the major isomer is shown) δ[ppm]: 1.46 (s, 9H) 2.22 (s, 3H), 3.06 (d, J=5.14 Hz, 3H), 6.47 (t,J=54.3 Hz, 1H) 11.74 (br s, 1H)

Intermediate 115 tert-butyl5-(difluoromethyl)-3-methyl-1H-pyrazole-4-carboxylate

Tert-butyl (2Z)-2-(difluoroacetyl)-3-(methylamino)but-2-enoate (10.0 g,40.1 mmol, 10:1 mixture with (2E)-Isomer) was dissolved in methanol (94mL) under an argon atmosphere and the resulting solution was cooled to−20° C. Hydrazine monohydrate (2.9 mL, 60 mmol) was added dropwise andthe reaction mixture stirred at −20° C. for 1 h and overnight at ambienttemperature. The reaction mixture was concentrated and the residueredissolved in ethyl acetate. The solution was washed with brine (3×)and the organic phase dried over sodium sulfate and concentrated toyield the desired product (6.70 g, 72% yield) that was used withoutfurther purification in the next step.

LC-MS (method 9): R_(t)=0.86 min; MS (ESIneg): m/z=231 [M−H]⁻

-   -   ¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: ¹H NMR (400 MHz,        dimethylsulfoxide-d₆) δ ppm 1.50 (s, 9H), 2.42 (s, 3H), 7.11 (t,        J=54.2 Hz, 1H), 13.24-13.68 (br s, 1H).

Intermediate 116 tert-butyl1-(6-chloropyrimidin-4-yl)-5-(difluoromethyl)-3-methyl-1H-pyrazole-4-carboxylate

4,6-Dichloropyrimidine (2.57 g, 17.2 mmol) and tert-butyl5-(difluoromethyl)-3-methyl-1H-pyrazole-4-carboxylate (4.00 g, 17 2mmol) were suspended in dimethylformamide (10 mL) under an argonatmosphere and cesium carbonate (5.61 g, 17.2 mmol) was added. Thereaction mixture was allowed to stir for 72 h at ambient temperature.The reaction mixture was poured into water (200 mL) and stirred for 30min. The precipitated solid was collected by filtration, washed withwater and dried to yield the desired product (4.4 g, 59% yield).

LC-MS (method 9): R_(t)=1.23 min; MS (ESIpos): m/z=345 [M±H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.55 (s, 9H), 2.94 (s,3H), 7.26 (t, J=53.4 Hz, 1H), 8.04 (s, 1H), 9.09 (s, 1H).

Intermediate 1171-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazolo[3,4-b]pyridine

4,6-Dichloropyrimidine (1.02 g, 6.88 mmol) and 3-methyl-1H-pyrazolo[3,4-b]pyridine (916 mg, 6.88 mmol) were suspended in dimethylformamide(8.4 mL) and cesium carbonate (2.24 g, 6.88 mmol) was added and thereaction mixture was stirred at ambient temperature overnight. Water (80mL) was added an stirring continued for 30 min. The precipitated solidwas collected by filtration, washed with water and dried to yield thedesired product (1.21g, 50% yield) as a 70:30 mixture with itsregioisomer 2-(6-chloropyrimidin-4-yl)-3-methyl-pyrazolo[3,4-b]pyridine.

LC-MS (method 10): R_(t)=1.07 min; MS (ESIpos): m/z=246 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.626 (16.00), 2.674(0.53), 3.051 (4.99), 3.112 (0.47), 3.129 (0.58), 7.119 (0.51), 7.129(0.57), 7.141 (0.64), 7.151 (0.63), 7.480 (1.32), 7.492 (1.51), 7.497(1.67), 7.509 (1.49), 8.325 (1.37), 8.349 (0.75), 8.420 (2.11), 8.439(2.08), 8.643 (2.73), 8.739 (0.85), 8.754 (2.53), 8.766 (2.51), 8.985(3.46), 9.128 (1.23).

Intermediate 118 1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazolo[3,4-c]pyridine

4,6-dichloropyrimidine (559 mg, 3.76 mmol) and3-methyl-1H-pyrazolo[3,4-c]pyridine (500 mg, 3.76 mmol) were suspendedin dimethylformamide (4.6 mL), cesium carbonate (1.22 g, 3.76 mmol) wasadded and the reaction mixture stirred at ambient temperature overnight.Water was added and the mixture stirred for another 30 min. Theprecipitated solid was collected by filtration, washed with water anddried under high vacuum to yield the desired product (670 mg, 62% yield,85% purity).

LC-MS (method 10): R_(t)=1.67 min; MS (ESIpos): m/z=246 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.321 (1.43), 2.399(2.82), 2.448 (1.25), 2.663 (16.00), 2.715 (1.63), 2.732 (0.85), 2.813(2.92), 2.892 (0.73), 3.044 (0.70), 3.112 (1.11), 7.592 (1.17), 7.761(0.97), 7.957 (7.17), 7.970 (3.35), 8.559 (2.67), 8.572 (2.82), 8.597(0.84), 8.611 (1.08), 8.630 (1.13), 8.940 (0.87), 9.042 (4.58), 9.509(0.67), 10.001 (4.18).

Intermediate 1194-(4-bromo-3,5-dimethyl-1H-pyrazol-1-yl)-6-chloropyrimidine

4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (300 mg, 1.44 mmol)was dissolvedn in acetonitrile (6.0 mL) and 1-bromopyrrolidine-2,5-dione(307 mg, 1.73 mmol) was added. The reaction mixture was stirred atambient temperature overnight. Water was added to precipitate and themixture was stirred for 5 minutes. The precipitated solid was collectedby filtration, washed with water, dried overnight in a high-vacuum ovenat 40° C. to yield the desired product (373 mg, 90% yield).

LC-MS (method 9): R_(t)=1.19 min; MS (ESIpos): m/z=288 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.227 (0.61), 2.258(11.76), 2.262 (15.88), 2.662 (0.76), 2.687 (12.00), 2.690 (16.00),7.941 (3.30), 8.955 (3.01).

Intermediate 1202-[1-(cyclopropylmethyl)-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]-1H-isoindole-1,3(2H)-dione

A sloution of2-[4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(5.00 g, 14.9 mmol) and (9.72 g, 29.8 mmol) in dimethylformamide (51 ml,660 mmol) was treated with (bromomethyl)cyclopropane (4.3 ml, 45 mmol).The resulting mixture was stirred overnight at ambient temperature.Water was added and the mixture was extracted three times with ethylacetate. The combined organic phases were washed with brine, dried oversodium sulfate and concentrated under reduced pressure. The crudeproduct was purified by preparative HPLC (column: Daicel Chiralcel OX-H;250*20 mm, 5 μM, flow 15 mL/min, gradient n-heptane/ethanol 50/50) toyield 1.73 g of the desired product (30%) together with its regioisomer(2.96 g, 48%).

LC-MS (method 10): R_(t)=2.21 min; MS (ESIpos): m/z=390 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.103 (1.38), 0.112(4.98), 0.115 (4.07), 0.122 (4.35), 0.124 (4.60), 0.133 (1.43), 0.409(1.59), 0.417 (4.05), 0.421 (3.97), 0.425 (2.04), 0.430 (2.13), 0.433(4.07), 0.436 (3.81), 0.446 (1.30), 0.802 (6.97), 0.817 (16.00), 0.832(6.97), 1.056 (0.51), 1.058 (0.48), 1.066 (0.95), 1.068 (0.89), 1.072(0.94), 1.075 (0.78), 1.082 (1.52), 1.088 (0.76), 1.091 (0.86), 1.096(0.83), 1.098 (0.83), 1.105 (0.40), 1.107 (0.40), 2.083 (1.05), 2.196(1.77), 2.211 (5.34), 2.226 (5.18), 2.242 (1.59), 3.329 (10.70), 3.867(7.22), 3.881 (7.03), 7.379 (0.52), 7.385 (3.62), 7.389 (1.37), 7.398(1.88), 7.403 (7.73), 7.407 (1.67), 7.416 (1.47), 7.420 (4.30), 7.426(0.49), 7.545 (0.69), 7.551 (4.30), 7.555 (1.98), 7.562 (4.76), 7.568(4.05), 7.575 (1.63), 7.579 (3.48), 7.944 (0.43), 7.947 (0.60), 7.954(5.16), 7.960 (5.38), 7.965 (4.71), 7.971 (7.64), 7.979 (1.13), 7.981(0.92), 8.007 (1.05), 8.009 (1.20), 8.017 (8.38), 8.023 (5.07), 8.028(5.68), 8.034 (4.99).

Intermediate 1211-(cyclopropylmethyl)-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-amine

A solution of2-[1-(cyclopropylmethyl)-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]-1H-isoindole-1,3(2H)-dione(1.73 g, 4.44 mmol) in ethanol (30 ml, 520 mmol) was treated withhydrazine monohydrate (1.1 ml, 22 mmol). The mixture was refluxedovernight. After cooling to room temperature a withe solid occurred withwas filtered of The filtrate was concentrated under reduced pressure.The crude product resolved in acetonitrile, the precipitate was againremoved by filtration and the filtrate was taken to dryness to obtain1.15 g of the desired product (90%).

LC-MS (method 9): R_(t)=0.86 min; MS (ESIpos): m/z=260 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.015 (1.55), −0.012(1.57), 0.005 (13.53), 0.021 (1.78), 0.317 (1.59), 0.321 (1.56), 0.331(6.50), 0.342 (2.99), 0.351 (6.61), 0.362 (1.48), 0.888 (7.30), 0.907(16.00), 0.925 (7.84), 0.938 (0.89), 0.955 (1.48), 0.958 (1.46), 0.962(1.37), 0.971 (1.99), 0.983 (1.33), 0.987 (1.36), 0.991 (1.35), 1.003(0.66), 2.141 (2.52), 2.159 (7.42), 2.178 (7.18), 2.197 (2.27), 3.511(9.88), 3.528 (9.75), 4.459 (11.57), 7.289 (1.71), 7.293 (1.71), 7.311(7.59), 7.315 (6.56), 7.332 (12.07), 7.343 (8.93), 7.365 (1.47).

Intermediate 122 4-(2-cyanobutanoyl)benzonitrile

A solution of butanenitrile (10 ml, 110 mmol) in tetrahydrofuran (170ml, 2.1 mol) was treated with lithium bis(trimethylsilyl)amide (1.0 M intetrahydrofuran; 120 mL, 1.0 M, 120 mmol) at 30° C. Afterwards ethyl4-cyanobenzoate (10.0 g, 57.1 mmol) was added dropwise. The resultingmixture was stirred for 4 hours. The reaction was quenched by theaddition of water and extracted once with dichloromethane. The aqueousphase was acidified with aqueous hydrochloric acid to pH 2 andsubsequently extracted three times with dichloromethane. The combinedorganic phases were dried over sodium sulphate and the solvent wasremoved under reduced pressure. The crude product was purified by flashchromatography on silica gel (solvent dichloromethane). Fractionscontaining the desired product were collected, the solvent was removedand the product was triturated with diethyl ether to yield 8.51 g of thedesired product (75%).

LC-MS (method 10): R_(t)=1.50 min; MS (ESIneg): m/z=197 [M−H]⁻

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.973 (1.48), 0.991(6.78), 1.008 (11.80), 1.027 (6.35), 1.043 (0.86), 1.068 (7.61), 1.087(16.00), 1.106 (7.94), 1.753 (0.68), 1.771 (1.14), 1.788 (1.47), 1.807(1.62), 1.825 (1.05), 1.909 (0.62), 1.928 (1.78), 1.937 (1.24), 1.946(1.87), 1.955 (1.45), 1.972 (1.02), 1.990 (0.68), 2.296 (2.58), 2.315(7.53), 2.333 (7.39), 2.352 (2.34), 3.375 (0.44), 3.392 (0.41), 5.194(1.84), 5.206 (2.09), 5.214 (1.95), 5.226 (1.69), 5.753 (1.44), 7.583(1.42), 7.603 (1.62), 7.726 (7.45), 7.747 (9.12), 7.948 (9.70), 7.968(8.16), 8.067 (4.07), 8.088 (6.82), 8.151 (7.11), 8.172 (4.68), 11.133(1.45).

Intermediate 1234-[5-amino-1-(cyclopropylmethyl)-4-ethyl-1H-pyrazol-3-yl]benzonitrile

A solution of 4-(2-cyanobutanoyl)benzonitrile (2.00 g, 10.1 mmol) and(cyclopropylmethyl)hydrazine dihydrochloride (2.09 g, 13.1 mmol) inethanol (20 ml, 340 mmol) was treated with N,N-diisopropylethylamine(4.6 ml, 26 mmol) and refluxed overnight. The conversion was not fullycompleted, therefore the mixture was left for 2 days, than additionaldi-isopropyl ethyl amine (2.28 mL, 13 1 mmol) was added and it wasrefluxed for another night. After cooling to ambient temperature themixture was concentrated and the remaining material was partitionedbetween water and ethyl acetate. The organic phase was washed withsaturated sodium carbonate solution, water, and brine and dried oversodium sulphate. The organic phase was concentrated under reducedpressure. The crude material was purified via preparative HPLC (method:column: Reprosil C18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent: A=water(0.01% formic acid), B=acetonitrile/gradient: 0.00-5.00 min=10% B, 6.50min=20% B, 17.0-19.75 min=100% B, 19.75-23.00 min=90% B) to yield thedesired product (1.1.9 g, 39%).

LC-MS (method 10): R_(t)=1.60 min; MS (ESIpos): m/z=267 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.343 (1.68), 0.356(6.33), 0.368 (7.09), 0.380 (2.23), 0.395 (0.63), 0.404 (0.71), 0.416(1.20), 0.430 (2.95), 0.439 (5.68), 0.459 (5.80), 0.475 (1.26), 0.558(0.44), 0.917 (0.65), 0.936 (0.74), 0.955 (1.06), 0.969 (1.05), 0.988(0.74), 1.007 (7.45), 1.026 (16.00), 1.044 (7.32), 1.106 (0.44), 1.133(0.50), 1.152 (1.20), 1.170 (1.26), 1.189 (1.04), 1.203 (1.52), 1.210(1.38), 1.222 (2.06), 1.234 (1.37), 1.239 (1.32), 1.252 (0.66), 1.989(0.56), 2.441 (0.42), 2.471 (2.48), 3.165 (0.46), 3.178 (0.47), 3.316(12.97), 3.817 (9.79), 3.834 (9.55), 5.020 (12.64), 7.582 (0.45), 7.603(0.50), 7.677 (0.59), 7.694 (0.74), 7.746 (7.11), 7.767 (13.35), 7.807(12.82), 7.827 (6.69), 7.849 (0.58), 7.859 (0.41), 7.953 (0.79), 7.973(0.73), 7.988 (0.45), 8.009 (0.61), 8.054 (0.56).

Intermediate 1242-[4-chloro-1-(cyclopropylmethyl)-5-(4-fluorophenyl)-1H-pyrazol-3-yl]-1H-isoindole-1,3(2H)-dione

A solution of2-[4-chloro-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(1.41 g, 4.13 mmol) in dimethylformamide (10 ml, 130 mmol) was treatedwith cesium carbonate (2.69 g, 8.25 mmol) and (bromomethyl)cyclopropane(1.2 ml, 12 mmol). The mixture was stirred overnight at ambienttemperature. The mixture was portioned between water and ethyl acetate.The organic phase was washed with water and brine, dried over sodiumsulfate. The solvent was removed under reduced pressure and the crudeproduct was purified by flash chromatography on silica gel(dichloromethane/ethyl acetate) to yield 328 mg of the desired product(18%) along with its regioisomer (360 mg, 20%).

LC-MS (method 14): R_(t)=1.17 min; MS (ESIpos): m/z=396 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (0.79), 0.006(0.57), 0.148 (2.46), 0.157 (9.48), 0.160 (7.73), 0.166 (8.39), 0.169(8.90), 0.178 (2.64), 0.437 (2.80), 0.445 (7.43), 0.449 (7.31), 0.453(3.76), 0.461 (7.76), 0.464 (7.28), 0.473 (2.45), 1.086 (0.66), 1.090(0.97), 1.095 (0.67), 1.099 (1.83), 1.106 (1.77), 1.109 (1.46), 1.115(2.88), 1.122 (1.44), 1.125 (1.64), 1.129 (1.66), 1.136 (0.60), 1.139(0.82), 1.145 (0.55), 2.468 (0.62), 2.482 (1.64), 2.496 (1.94), 3.335(9.81), 4.020 (13.86), 4.034 (13.82), 4.171 (1.59), 4.185 (2.82), 4.199(1.49), 4.980 (2.68), 5.003 (1.22), 5.013 (1.17), 5.016 (0.86), 5.616(0.59), 5.635 (0.49), 5.638 (0.45), 5.648 (0.45), 5.652 (0.43), 5.670(0.49), 5.761 (3.10), 7.433 (0.91), 7.439 (7.17), 7.442 (3.91), 7.447(1.37), 7.456 (15.46), 7.460 (6.28), 7.470 (2.96), 7.474 (8.54), 7.478(2.67), 7.638 (1.81), 7.642 (0.89), 7.649 (2.25), 7.652 (2.09), 7.658(8.27), 7.662 (4.15), 7.669 (8.92), 7.676 (7.61), 7.682 (3.18), 7.686(6.74), 7.692 (0.77), 7.969 (0.84), 7.972 (1.17), 7.979 (10.94), 7.985(11.67), 7.990 (11.12), 7.996 (16.00), 8.004 (2.35), 8.006 (1.88), 8.039(2.08), 8.041 (2.16), 8.049 (15.04), 8.054 (10.57), 8.059 (10.65), 8.066(9.24), 8.073 (0.85), 8.076 (0.58).

Intermediate 1254-chloro-1-(cyclopropylmethyl)-5-(4-fluorophenyl)-1H-pyrazol-3-amine

A solution of2-[4-chloro-1-(cyclopropylmethyl)-5-(4-fluorophenyl)-1H-pyrazol-3-yl]-1H-isoindole-1,3(2H)-dione(328 mg, 829 μmol) in ethanol (5.7 ml, 97 mmol) was treated withhydrazine monohydrate (200 μl, 4.1 mmol). The mixture was stirredovernight at 90° C. After cooling to ambient temperature the mixture wasportioned between water and ethyl acetate. The aqueous was extractedadditionally two times with ethyl acetate. The combined organic phaseswere washed with 1M aqueous sodium hydrogen carbonate solution and brineand dried over sodium sulfate. The solvent was removed under reducedpressure to yield the desired crude product (204 mg, 68%).

LC-MS (method 10): R_(t)=1.77 min; MS (ESIpos): m/z=266 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (0.73), 0.006(0.55), 0.021 (2.43), 0.031 (9.25), 0.033 (7.72), 0.040 (8.38), 0.043(8.72), 0.052 (2.68), 0.347 (2.92), 0.356 (7.67), 0.359 (7.63), 0.363(3.80), 0.368 (4.03), 0.371 (7.76), 0.375 (7.42), 0.384 (2.59), 0.712(2.71), 0.727 (6.68), 0.742 (3.24), 0.966 (0.73), 0.971 (0.93), 0.973(0.85), 0.976 (0.67), 0.980 (1.73), 0.983 (1.65), 0.987 (1.71), 0.990(1.44), 0.997 (2.77), 1.003 (1.43), 1.006 (1.60), 1.010 (1.59), 1.012(1.52), 1.017 (0.61), 1.020 (0.78), 1.022 (0.76), 1.026 (0.59), 1.060(0.48), 1.064 (0.91), 1.079 (1.48), 1.094 (1.47), 1.109 (0.84), 1.533(0.42), 1.548 (1.12), 1.562 (1.54), 1.577 (1.10), 3.329 (11.01), 3.642(14.68), 3.656 (14.26), 3.749 (1.55), 3.763 (2.85), 3.777 (1.67), 4.901(4.50), 4.914 (16.00), 7.346 (0.90), 7.352 (6.62), 7.355 (3.55), 7.359(1.25), 7.365 (3.66), 7.369 (15.65), 7.372 (6.12), 7.383 (2.99), 7.387(9.44), 7.390 (3.02), 7.442 (0.40), 7.447 (2.29), 7.451 (1.86), 7.457(9.35), 7.461 (4.60), 7.468 (9.97), 7.475 (7.44), 7.481 (2.99), 7.485(6.25), 7.491 (0.70).

Intermediate 1262-[4-chloro-1-(cyclopropylmethyl)-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione

A solution of2-[4-chloro-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(1.41 g, 4.13 mmol) in dimethylformamide (10 ml, 130 mmol) was treatedwith cesium carbonate (2.69 g, 8.25 mmol) and (bromomethyl)cyclopropane(1.2 ml, 12 mmol). The mixture was stirred overnight at ambienttemperature. The mixture was portioned between water and ethyl acetate.The organic phase was washed with water and brine, dried over sodiumsulfate. The solvent was removed under reduced pressure and the crudeproduct was purified by flash chromatography on silica gel(dichloromethane/ethyl acetate) to yield 360 mg of the desired product(20%) along with its regioisomer (320 mg, 18%).

LC-MS (method 14): R_(t)=1.24 min; MS (ESIpos): m/z=396 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.007 (1.08), 0.317(2.07), 0.326 (8.24), 0.329 (7.16), 0.336 (7.98), 0.338 (7.88), 0.347(2.69), 0.453 (2.72), 0.461 (6.80), 0.464 (6.64), 0.469 (3.68), 0.477(7.06), 0.481 (6.41), 0.490 (2.04), 1.237 (0.66), 1.242 (0.98), 1.252(1.81), 1.258 (1.72), 1.261 (1.44), 1.268 (2.74), 1.274 (1.45), 1.277(1.62), 1.283 (1.69), 1.292 (0.84), 1.298 (0.55), 2.088 (1.24), 2.520(0.77), 2.523 (0.92), 2.566 (0.54), 3.327 (16.00), 4.042 (13.04), 4.056(12.66), 4.223 (1.46), 4.238 (2.31), 4.252 (1.42), 4.980 (0.89), 4.983(0.88), 5.001 (0.92), 5.004 (0.95), 5.048 (0.90), 5.052 (0.86), 5.082(1.02), 5.086 (0.93), 5.732 (0.56), 5.752 (0.74), 5.766 (0.75), 5.787(0.49), 7.339 (2.45), 7.345 (7.14), 7.348 (2.73), 7.357 (5.65), 7.362(14.66), 7.366 (3.24), 7.376 (3.56), 7.380 (7.52), 7.386 (0.86), 7.899(1.84), 7.904 (1.11), 7.913 (8.22), 7.917 (4.98), 7.924 (8.87), 7.928(6.24), 7.931 (7.77), 7.937 (3.23), 7.942 (6.85), 7.948 (0.78), 8.002(1.16), 8.009 (9.68), 8.015 (10.42), 8.020 (10.52), 8.027 (13.72), 8.034(2.00), 8.082 (1.54), 8.083 (1.79), 8.092 (13.13), 8.097 (12.13), 8.102(11.51), 8.109 (10.12), 8.114 (2.48), 8.119 (0.69).

Intermediate 1274-chloro-1-(cyclopropylmethyl)-3-(4-fluorophenyl)-1H-pyrazol-5-amine

A solution of2-[4-chloro-1-(cyclopropylmethyl)-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(360 mg, 909 μmol) in ethanol (8.4 ml, 140 mmol) was treated withhydrazine monohydrate (220 μl, 4.5 mmol). The mixture was stirredovernight at 90° C. After cooling to ambient temperature the mixture wasportioned between water and ethyl acetate. The aqueous was extractedadditionally two times with ethyl acetate. The combined organic phaseswere washed with 1M aqueous sodium hydrogen carbonate solution and brineand dried over sodium sulphate. The solvent was removed under reducedpressure to yield the desired crude product (236 mg, 79%).

LC-MS (method 10): R_(t)=1.86 min; MS (ESIpos): m/z=266 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.348 (1.49), 0.361(6.51), 0.373 (7.67), 0.385 (2.45), 0.405 (0.61), 0.423 (0.70), 0.440(2.31), 0.450 (5.63), 0.470 (6.14), 0.485 (1.45), 0.875 (1.59), 0.894(3.55), 0.912 (1.84), 1.185 (0.82), 1.198 (1.57), 1.205 (1.45), 1.216(2.28), 1.229 (1.48), 1.234 (1.60), 1.246 (0.87), 1.263 (0.73), 1.281(1.03), 1.300 (1.00), 1.319 (0.55), 1.653 (0.77), 1.672 (1.07), 1.690(0.72), 3.843 (11.37), 3.860 (11.20), 3.916 (1.03), 3.934 (1.83), 3.951(0.98), 5.503 (16.00), 5.541 (0.68), 7.221 (5.38), 7.244 (10.59), 7.266(5.40), 7.785 (1.92), 7.793 (6.18), 7.798 (3.89), 7.807 (7.89), 7.815(6.62), 7.824 (3.07), 7.829 (5.44).

Intermediate 1282-[1-(cyclopropylmethyl)-5-(4-fluorophenyl)-4-methyl-1H-pyrazol-3-yl]-1H-isoindole-1,3(2H)-dione

A solution of2-[5-(4-fluorophenyl)-4-methyl-1H-pyrazol-3-yl]-1H-isoindole-1,3(2H)-dione(1.26 g, 3.93 mmol) in dimethylformamide (10 ml, 130 mmol) was treatedwith cesium carbonate (2.56 g, 7.87 mmol) and (bromomethyl)cyclopropane(1.1 ml, 12 mmol). The mixture was stirred overnight at ambienttemperature. The mixture was portioned between water and ethyl acetate.The organic phase was washed with water and brine, dried over sodiumsulfate. The solvent was removed under reduced pressure and the crudeproduct was purified by flash chromatography on silica gel(dichloromethane/ethyl acetate) to yield 513 mg of the desired product(30%) along with its regioisomer (848 mg, 48%).

LC-MS (method 10): R_(t)=2.11 min; MS (ESIpos): m/z=376 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.43), 0.092(0.67), 0.103 (2.77), 0.106 (2.47), 0.118 (2.86), 0.129 (0.85), 0.387(0.83), 0.398 (2.20), 0.402 (2.33), 0.407 (1.24), 0.418 (2.33), 0.422(2.32), 0.433 (0.74), 1.046 (0.51), 1.053 (0.51), 1.065 (0.82), 1.077(0.49), 1.083 (0.49), 1.794 (16.00), 1.989 (0.69), 2.460 (0.41), 2.524(0.53), 3.914 (4.13), 3.932 (4.08), 4.056 (0.45), 4.074 (0.63), 7.376(1.89), 7.398 (4.35), 7.420 (2.60), 7.528 (0.47), 7.544 (2.68), 7.550(1.54), 7.558 (2.79), 7.566 (2.44), 7.574 (0.91), 7.580 (1.94), 7.936(2.60), 7.944 (2.98), 7.950 (2.95), 7.958 (4.87), 7.967 (0.90), 7.988(0.78), 7.998 (4.45), 8.005 (2.70), 8.012 (2.76), 8.019 (2.31).

Intermediate 1292-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione

A solution of2-[3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(1.26 g, 3.93 mmol) in dimethylformamide (10 ml, 130 mmol) was treatedwith cesium carbonate (2.56 g, 7.87 mmol) and (bromomethyl)cyclopropane(1.1 ml, 12 mmol). The mixture was stirred overnight at ambienttemperature. The mixture was portioned between water and ethyl acetate.The organic phase was washed with water and brine, dried over sodiumsulfate. The solvent was removed under reduced pressure and the crudeproduct was purified by flash chromatography on silica gel(dichloromethane/ethyl acetate) to yield 848 mg of the desired product(48%) along with its regioisomer (513 mg, 30%).

LC-MS (method 10): R_(t)=2.18 min; MS (ESIpos): m/z=376 [M+H]⁺

Intermediate 1301-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine

A solution of2-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(3.70 g, 9.86 mmol) in ethanol (90 ml, 1.5 mol) was treated withhydrazine monohydrate (2.4 ml, 49 mmol). The mixture was stirredovernight at 90° C. After cooling to ambient temperature the mixture wasportioned between water and ethyl acetate. The aqueous phase wasextracted twice with ethyl acetate. The combined organic phase s werewashed with 1.0 M aqueous sodium hydrogen carbonate solution, brine anddried over sodium sulfate. The solution was concentrated to yield thedesired product (2.37 g, 96%).

LC-MS (method 9): R_(t)=0.72 min; MS (ESIpos): m/z=246 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.330 (0.48), 0.342(1.93), 0.346 (1.95), 0.354 (2.33), 0.357 (2.12), 0.367 (0.93), 0.411(0.92), 0.420 (1.80), 0.424 (1.53), 0.431 (1.19), 0.440 (2.01), 0.444(1.53), 0.456 (0.55), 1.180 (0.47), 1.188 (0.45), 1.200 (0.75), 1.212(0.44), 1.217 (0.44), 1.975 (16.00), 3.787 (4.04), 3.804 (3.98), 4.905(4.30), 7.164 (2.01), 7.170 (0.70), 7.181 (0.91), 7.187 (4.12), 7.192(0.88), 7.204 (0.74), 7.209 (2.23), 7.578 (2.22), 7.584 (0.94), 7.593(2.45), 7.601 (2.27), 7.609 (0.83), 7.615 (2.00).

Intermediate 1311-(cyclopropylmethyl)-5-(4-fluorophenyl)-4-methyl-1H-pyrazol-3-amine

A solution of2-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(517 mg, 1.38 mmol) in ethanol (11 ml, 180 mmol) was treated withhydrazine monohydrate (330 μl, 6.9 mmol). The mixture was stirredovernight at 90° C. After cooling to ambient temperature the mixture wasportioned between water and ethyl acetate. The aqueous phase wasextracted twice with ethyl acetate. The combined organic phases werewashed with 1.0 M aqueous sodium hydrogen carbonate solution, brine anddried over sodium sulfate. The solution was concentrated to yield thedesired product (314 mg, 77%).

LC-MS (method 10): R_(t)=1.51 min; MS (ESIpos): m/z=246 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.019 (0.73), −0.008(3.14), 0.018 (0.73), 0.304 (0.80), 0.315 (2.28), 0.318 (2.17), 0.324(1.08), 0.335 (2.34), 0.350 (0.66), 0.703 (0.57), 0.721 (1.31), 0.739(0.69), 0.941 (0.56), 0.948 (0.52), 0.961 (0.82), 0.973 (0.48), 0.978(0.50), 1.530 (0.40), 1.728 (4.37), 1.733 (16.00), 3.317 (5.54), 3.560(4.30), 3.577 (4.23), 3.681 (0.69), 4.483 (4.40), 7.290 (1.15), 7.312(4.02), 7.334 (4.22), 7.339 (3.93), 7.353 (3.46), 7.360 (1.75), 7.369(0.61), 7.375 (0.98).

Intermediate 1322-[1-(2,2-difluoroethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione

A solution of2-[4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(2.50 g, 7.46 mmol) in dimethylformamide (32 ml, 420 mmol) was treatedwith cesium carbonate (4.86 g, 14.9 mmol) and 2,2-difluoroethyltrifluoromethanesulfonate (2.0 ml, 15 mmol). The mixture was stirredovernight at ambient temperature. One additional equivalent of2,2-difluoroethyl trifluoromethanesulfonate (0.99 mL, 7.45 mmol) wasadded and the mixture was again stirred at ambient temperature for 4hours. The mixture was portioned between water and ethyl acetate. Theorganic phase was washed with water and brine, dried over sodiumsulfate. The solvent was removed under reduced pressure and the crudeproduct was purified by flash chromatography on silica gel(dichloromethane/ethyl acetate 60:1, Biotage SNAP Ultra 50 g) to yield1.20 g of the desired product (40%) along with its regioisomer (655 mg,22%).

LC-MS (method 10): R_(t)=2.12 min; MS (ESIpos): m/z=400 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.897 (7.24), 0.916(16.00), 0.935 (7.14), 2.074 (2.49), 2.441 (2.14), 2.460 (6.26), 2.478(6.48), 2.524 (0.73), 4.572 (2.02), 4.581 (2.17), 4.608 (4.05), 4.618(4.02), 4.645 (2.03), 4.654 (1.80), 6.109 (0.67), 6.119 (1.32), 6.128(0.57), 6.246 (1.28), 6.256 (2.65), 6.265 (1.20), 6.384 (0.59), 6.393(1.21), 6.403 (0.59), 7.293 (4.33), 7.316 (8.52), 7.338 (4.46), 7.706(5.02), 7.712 (2.39), 7.720 (5.50), 7.728 (4.92), 7.737 (2.02), 7.742(4.22), 7.966 (0.87), 7.975 (5.05), 7.982 (5.52), 7.988 (5.61), 7.996(7.71), 8.006 (1.29), 8.042 (1.54), 8.052 (8.33), 8.059 (5.73), 8.066(5.45), 8.073 (4.65), 8.082 (0.42).

Intermediate 1332-[1-(2,2-difluoroethyl)-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]-1H-isoindole-1,3(2H)-dione

A solution of2-[4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(2.50 g, 7.46 mmol) in dimethylformamide (32 ml, 420 mmol) was treatedwith cesium carbonate (4.86 g, 14.9 mmol) and 2,2-difluoroethyltrifluoromethanesulfonate (2.0 ml, 15 mmol). The mixture was stirredovernight at ambient temperature. One additional equivalent of2,2-difluoroethyl trifluoromethanesulfonate (0.99 mL, 7.45 mmol) wasadded and the mixture was again stirred at ambient temperature for 4hours. The mixture was portioned between water and ethyl acetate. Theorganic phase was washed with water and brine, dried over sodiumsulfate. The solvent was removed under reduced pressure and the crudeproduct was purified by flash chromatography on silica gel(dichloromethane/ethyl acetate 60:1, Biotage SNAP Ultra 50 g) to yield655 mg of the desired product (22%) along with its regioisomer (1.20 g,40%).

LC-MS (method 10): R_(t)=2.08 min; MS (ESIpos): m/z=400 [M+H]⁺

Intermediate 1341-(2,2-difluoroethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-amine

A solution of2-[1-(2,2-difluoroethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(1.20 g, 3.00 mmol) in ethanol (20 ml, 340 mmol) was treated withhydrazine monohydrate (730 μl, 15 mmol). The mixture was stirredovernight at 90° C. After cooling to ambient temperature the mixture wasportioned between water and ethyl acetate. The aqueous phase wasextracted twice with ethyl acetate. The combined organic phases werewashed with 1.0 M aqueous sodium hydrogen carbonate solution, brine anddried over sodium sulfate. The solution was concentrated to yield thedesired product (800 mg, 98%).

LC-MS (method 10): R_(t)=1.62 min; MS (ESIpos): m/z=270 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.981 (7.32), 0.999(16.00), 1.018 (7.26), 2.428 (6.81), 2.446 (6.56), 2.465 (2.20), 4.355(2.48), 4.366 (2.63), 4.391 (4.85), 4.402 (4.81), 4.427 (2.47), 4.438(2.23), 5.147 (11.45), 6.147 (0.71), 6.158 (1.40), 6.169 (0.64), 6.286(1.39), 6.297 (2.80), 6.307 (1.30), 6.425 (0.66), 6.435 (1.32), 6.446(0.64), 7.190 (4.22), 7.212 (8.47), 7.234 (4.56), 7.549 (5.25), 7.554(2.68), 7.563 (6.04), 7.571 (5.38), 7.585 (4.46).

Intermediate 1351-(2,2-difluoroethyl)-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-amine

A solution of2-[1-(2,2-difluoroethyl)-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]-1H-isoindole-1,3(2H)-dione(655 mg, 1.64 mmol) in ethanol (10 ml, 170 mmol) was treated withhydrazine monohydrate (400 μl, 8.2 mmol). The mixture was stirredovernight at 90° C. After cooling to ambient temperature the mixture wasportioned between water and ethyl acetate. The aqueous phase wasextracted twice with ethyl acetate. The combined organic phases werewashed with 1.0 M aqueous sodium hydrogen carbonate solution, brine anddried over sodium sulfate. The solution was concentrated to yield thedesired product (470 mg, quant.).

LC-MS (method 10): R_(t)=1.69 min; MS (ESIpos): m/z=270 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.58), 0.894(4.65), 0.913 (10.80), 0.932 (4.95), 2.151 (1.41), 2.170 (4.35), 2.189(4.24), 2.207 (1.30), 3.992 (1.41), 4.002 (1.50), 4.028 (2.87), 4.038(2.88), 4.063 (1.44), 4.074 (1.33), 4.670 (5.64), 6.021 (0.42), 6.031(0.89), 6.159 (0.82), 6.170 (1.79), 6.180 (0.82), 6.309 (0.86), 6.319(0.41), 7.310 (0.44), 7.319 (0.44), 7.334 (9.33), 7.353 (16.00).

Intermediate 136 ethyl4-chloro-1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate

A solution of ethyl1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate (480 mg,1.80 mmol) in acetonitrile (8.8 ml, 170 mmol) was treated with1-chloropyrrolidine-2,5-dione (288 mg, 2.16 mmol). The mixture wasstirred 2 days at ambient temperature. Water was added and the mixturewas extracted with ethyl acetate (3×). The combined organic phases werewashed with water and brine, dried over sodium sulfate and concentratedunder reduced pressure. The crude product was purified by preparativeHPLC (method: column: Reprosil C18; 10 μm; 125×40 mm/flow: 75mL/min/solvent: A=water (0.1% formic acid), B=acetonitrile/gradient:0.00-5.50 min=10% B, 17.65-19.48 min=95% B, 19.66 min=10% B) to yield240 mg of the desired product (63%).

LC-MS (method 10): R_(t)=2.21 min; MS (ESIpos): m/z=301 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (2.12), 0.008(1.07), 1.240 (4.60), 1.258 (9.37), 1.276 (4.53), 2.322 (16.00), 2.524(0.58), 4.359 (1.55), 4.377 (4.54), 4.395 (4.45), 4.413 (1.41), 8.008(3.31), 8.947 (3.50).

Intermediate 1372-[1-(cyclobutylmethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione

A solution of2-[4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(2.00 g, 5.96 mmol) in dimethylformamide (26 ml, 340 mmol) was treatedwith cesium carbonate (3.89 g, 11.9 mmol) and (bromomethyl)cyclobutane(1.78 g, 11.9 mmol). The mixture was stirred overnight at ambienttemperature. The mixture was diluted with wateradn extracted with ethylacetate (3×). The combined organic phase s were washed with water andbrine and dried over sodium sulfate. The crude product was purifiedusing flash chromatography on silica gel (method: column: Biotage SnapUltra 25g/flow: 75 mL/min./solvent=dichloromethane (100%)) to obain 904mg of the desired product together with its regioisomer (320 mg, 13%).

LC-MS (method 10): R_(t)=2.44 min; MS (ESIpos): m/z=404 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.48), 0.008(1.25), 0.889 (6.83), 0.908 (16.00), 0.926 (7.12), 1.710 (0.71), 1.716(0.91), 1.732 (3.35), 1.744 (7.41), 1.752 (6.01), 1.758 (4.72), 1.761(4.97), 1.774 (1.98), 1.791 (1.33), 1.798 (0.89), 1.817 (0.66), 1.864(0.41), 1.879 (0.81), 1.892 (1.58), 1.903 (2.64), 1.908 (2.20), 1.918(2.75), 1.924 (3.44), 1.934 (1.06), 1.938 (0.99), 1.948 (0.42), 2.074(0.94), 2.406 (1.88), 2.425 (5.83), 2.443 (5.71), 2.462 (1.77), 2.524(0.45), 2.691 (0.47), 2.710 (1.26), 2.729 (1.39), 2.742 (0.92), 2.747(1.08), 2.766 (0.55), 4.001 (8.81), 4.019 (8.63), 7.267 (4.04), 7.289(8.37), 7.306 (1.57), 7.311 (4.50), 7.318 (0.51), 7.672 (0.59), 7.680(4.66), 7.685 (2.06), 7.694 (5.15), 7.702 (4.86), 7.710 (1.87), 7.716(4.23), 7.723 (0.49), 7.973 (0.51), 7.982 (4.84), 7.989 (5.33), 7.996(5.39), 8.003 (7.88), 8.013 (1.20), 8.049 (1.15), 8.059 (8.02), 8.067(5.27), 8.073 (5.36), 8.081 (4.66), 8.090 (0.40).

Intermediate 1381-(cyclobutylmethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-amine

A solution of2-[1-(cyclobutylmethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(900 mg, 2.23 mmol) in ethanol (280 ml, 4.8 mol) was treated withhydrazine monohydrate (540 μl, 11 mmol) and stirred overnight at 90° C.After cooling to ambient temperature the mixture was diluted with waterand extracted three times with ethyl acetate. The combined organicphases were washed with 1M aqueous sodium hydrogen carbonate solutionand brine, dried over sodium sulfate and concentrated under reducedpressure to yield the desired product (578 mg, 85%).

LC-MS (method 10): R_(t)=1.72 min; MS (ESIpos): m/z=274 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.976 (7.30), 0.995(16.00), 1.013 (7.27), 1.049 (0.65), 1.068 (1.28), 1.087 (0.59), 1.772(1.10), 1.780 (1.99), 1.798 (4.84), 1.816 (8.42), 1.825 (7.95), 1.840(3.63), 1.851 (1.37), 1.858 (1.67), 1.867 (1.09), 1.888 (0.45), 1.908(0.72), 1.934 (1.93), 1.945 (3.44), 1.950 (4.10), 1.966 (3.26), 2.002(0.42), 2.397 (2.32), 2.415 (6.73), 2.434 (6.53), 2.453 (2.17), 2.575(0.51), 2.689 (0.64), 2.707 (1.45), 2.724 (1.79), 2.745 (1.31), 2.764(0.71), 3.910 (9.91), 3.928 (9.51), 4.102 (0.80), 4.120 (0.68), 4.892(11.01), 7.160 (4.17), 7.182 (8.34), 7.204 (4.52), 7.236 (0.40), 7.258(0.79), 7.280 (0.50), 7.523 (0.96), 7.530 (5.29), 7.536 (2.55), 7.545(6.07), 7.552 (5.51), 7.561 (2.58), 7.566 (5.07), 7.629 (0.79), 7.636(0.43), 7.644 (0.66), 7.651 (0.59), 7.666 (0.46), 10.085 (0.49).

Intermediate 1394-[5-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-methyl-1H-pyrazol-3-yl]benzonitrile

4-(5-amino-4-methyl-1H-pyrazol-3-yl)benzonitrile (6.80 g, 34.3 mmol) and2-benzofuran-1,3-dione (7.62 g, 51.5 mmol) were suspended in acetic acid(150 mL) and the reaction mixture was heated to 120° C. bath temperatureovernight. After cooling to ambient temperature, methyl tert-butyletherwas added and the precipitated solid collected by filtration, furtherwashed with methyl tert-butylether and dried under high vacuum overnightand further in a drying oven under vacuum at 40° C. to yield the desiredproduct (11.7 g, 104% yield, contained 24% AcOH based on NMR).

LC-MS (method 10): R_(t)=1.60 min; MS (ESIpos): m/z=329 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.62), 0.008(1.32), 1.909 (12.37), 2.059 (16.00), 2.367 (0.43), 2.524 (1.09), 2.711(0.42), 7.842 (4.06), 7.863 (5.29), 7.945 (2.96), 7.953 (3.62), 7.959(3.95), 7.967 (5.31), 7.976 (1.61), 8.002 (6.36), 8.008 (6.35), 8.022(7.34), 13.648 (3.22).

Intermediate 1404-[5-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-1,4-dimethyl-1H-pyrazol-3-yl]benzonitrileas mixture with4-[3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-1,4-dimethyl-1H-pyrazol-5-yl]benzonitrile

A solution of4-[3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-methyl-1H-pyrazol-5-yl]benzonitrile(14.1 g, 42.9 mmol) in dimethylformamide (140 ml, 1.8 mol) was treatedwith cesium carbonate (27.9 g, 85.8 mmol) and iodomethane (5.3 ml, 86mmol) at −20° C. The mixture was allowed to warm up to ambienttemperature and stirred for 2 hours. The mixture was diluted with waterand extracted with ethyl acetate (3×). The combined organic phase s werewashed with water (2×), brine and dried over sodium sulfate. Separationof the regioisomers was partially possible by titruation withacetonitrile: 1.52 g (8%, 92% pure) of pure4-[3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-1,4-dimethyl-1H-pyrazol-5-yl]benzonitrile0.19 g (1%) of pure-[5-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-1,4-dimethyl-1H-pyrazol-3-yl]benzonitrileand 5.75 g (31%) of the regioisomeric mixture were obtained.

LC-MS (method 11,4-[3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-1,4-dimethyl-1H-pyrazol-5-yl]benzonitrile):R_(t)=1.23 min; MS (ESIpos): m/z=343 [M+H]⁺

LC-MS (method 11,4-[5-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-1,4-dimethyl-1H-pyrazol-3-yl]benzonitrile):R_(t)=1.29 min; MS (ESIpos): m/z=343 [M+H]⁺

Intermediate 141 4-(5-amino-1,4-dimethyl-1H-pyrazol-3-yl)benzonitrile

A solution of4-[5-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-1,4-dimethyl-1H-pyrazol-3-yl]benzonitrile/4-[3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-1,4-dimethyl-1H-pyrazol-5-yl]benzonitrileapprox. 1:1 (5.85 g, 17.1 mmol) in ethanol (150 ml, 2.6 mol) was treatedwith hydrazine monohydrate (4.2 ml, 85 mmol). The mixture was reluxedfor 2.5 hours. After cooling to room temperature the mixture was dilutedwith water and extracted with ethyl acetate (3×). The combined organicphase s were washed with 1M aqueous sodium hydrogen carbonate solution,brine, dried over sodium sulfate and concentrated under reducedpressure. 3.2 g of the regioisomeric mixture were separated into theregioisomers (column: Chiralpak IG, 5 μM, 250×20 mm, flow: 15 mL/min,n-heptane/ethanol 30/70) to yield 2.30 g of the desired product (63%)together with its regioisomer (680 mg, 19%).

LC-MS (method 11): R_(t)=0.85 min; MS (ESIpos): m/z=213 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.066 (11.06), 3.422(0.66), 5.091 (3.28), 7.810 (16.00).

Intermediate 142 4-(3-amino-1,4-dimethyl-1H-pyrazol-5-yl)benzonitrile

A solution of4-[5-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-1,4-dimethyl-1H-pyrazol-3-yl]benzonitrile/4-[3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-1,4-dimethyl-1H-pyrazol-5-yl]benzonitrileapprox. 1:1 (5.85 g, 17.1 mmol) in ethanol (150 ml, 2.6 mol) was tretaedwith hydrazine monohydrate (4.2 ml, 85 mmol). The mixture was reluxedfor 2.5 hours. After cooling to room temperature the mixture was dilutedwith water and extracted with ethyl acetate (3×). The combined organicphase s were washed with 1M aqueous sodium hydrogen carbonate solution,brine, dried over sodium sulfate and concentrated under reducedpressure. 3.2 g of the regioisomeric mixture were separated into theregioisomers (column: Chiralpak IG, 5 μM, 250×20 mm, flow: 15 mL/min,n-heptane/ethanol 30/70) to yield 680 mg of the desired product (19%)together with its regioisomer (2.30 g, 63%).

LC-MS (method 11): R_(t)=0.82 min; MS (ESIpos): m/z=213 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.818 (16.00), 2.091(0.42), 3.367 (2.38), 4.572 (4.39), 7.571 (4.29), 7.575 (1.55), 7.584(1.73), 7.588 (4.52), 7.591 (0.88), 7.946 (1.05), 7.949 (4.66), 7.953(1.57), 7.963 (1.63), 7.966 (4.13), 7.970 (0.75).

Intermediate 143 4-(3,5-dimethyl-4-nitro-1H-pyrazol-1-yl)benzonitrile

A solution of 3,5-dimethyl-4-nitro-1H-pyrazole (5.00 g, 35.4 mmol) and(4-cyanophenyl)boronic acid (5.21 g, 35.4 mmol) in dichloromethane (50ml, 780 mmol) was treated with anhydrous cupric acetate (9.65 g, 53.1mmol), pyridine (29 ml, 350 mmol) and molecular sieves (7.93 g). Themixture was stirred under an argon atmosphere at ambient temperature for2 days. The mixture was filtered over a pad of kieselgur, the remainngfilter cake was washed with dichloromethane. The filtrate was washedwith water, dried over sodium sulfate and concentrated under reducedpressure. The crude product was purified by falsh-chromatography onsilics gel (dichloromethane/ethyl acetate 40:1, column: SNAP Ultra 100g) to yield 2.60 g (30%) of the desired product.

LC-MS (method 9): R_(t)=0.88 min; MS (ESIpos): m/z=243 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.625 (16.00), 7.797(0.49), 7.802 (3.48), 7.807 (1.24), 7.819 (1.33), 7.824 (4.13), 7.829(0.63), 8.076 (0.59), 8.081 (3.97), 8.086 (1.28), 8.098 (1.17), 8.103(3.35), 8.109 (0.49).

Intermediate 144 4-(4-amino-3,5-dimethyl-1H-pyrazol-1-yl)benzonitrile

A solution of 4-(3,5-dimethyl-4-nitro-1H-pyrazol-1-yl)benzonitrile (2.60g, 10.7 mmol) in methanol (100 ml) was treated with aqueous hydrochloricacid (20 ml, 12 M, 240 mmol) and iron (3.00 g, 53.7 mmol). The mixturewas refluxed for 2 hours. The reaction mixture was filtered. Thefiltrate was neutralized with saturated aqueous sodium hydrogencarbonate solution an extracted with ethyl acetate (3×). The combinedorganic phases were washed with saturated aqueous sodium hydrogencarbonate solution, brine, dried over sodium sulfate and concentratedunder reduced pressure to yield 1.70 g (63%) of the desired product.

LC-MS (method 10): R_(t)=0.73 min; MS (ESIpos): m/z=213 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.074 (0.73), 2.107(16.00), 2.283 (14.84), 2.409 (0.41), 3.848 (1.72), 3.858 (2.53), 7.613(0.43), 7.634 (0.45), 7.663 (3.45), 7.685 (4.10), 7.858 (3.83), 7.879(3.01), 7.988 (0.63), 8.009 (0.44).

Intermediate 145 4-(3-amino-4-ethyl-1H-pyrazol-5-yl)benzonitrile

A solution of 4-(2-cyanobutanoyl)benzonitrile (3.88 g, 19 5 mmol) inethanol (50 ml, 860 mmol) was treated with hydrazine hydrate (1:1) (1.1ml, 23 mmol) and refluxed overnight. After cooling to ambienttemperature the mixture was diluted with saturated sodium hydrogencarbonate solution. Ethanol was removed under reduced pressure, theoccurring precipitate was collected by filtration, washed with water anddried to yield the desired product (4.06 g, 98%).

LC-MS (method 10): R_(t)=1.09 min; MS (ESIpos): m/z=213 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.022 (8.30), 1.040(16.00), 1.058 (7.78), 2.452 (3.40), 2.470 (8.84), 2.489 (9.63), 4.650(1.64), 7.695 (5.47), 7.713 (6.04), 7.859 (7.60), 7.878 (5.87), 11.790(2.67).

Intermediate 1464-[3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-ethyl-1H-pyrazol-5-yl]benzonitrile

4-(3-amino-4-ethyl-1H-pyrazol-5-yl)benzonitrile (3.00 g, 14.1 mmol) and2-benzofuran-1,3-dione (3.14 g, 21.2 mmol) were treated with acetic acid(25 ml, 440 mmol) and stirred overnight at 140° C. After cooling toambient temperature the mixture was diluted with water. The occurringprecipitate was collected by filtration, washed with water and dried toyield 4.92 g (98%) of the desired product.

LC-MS (method 10): R_(t)=1.88 min; MS (ESIpos): m/z=343 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.950 (5.55), 0.968(11.73), 0.987 (5.71), 1.919 (16.00), 7.833 (3.92), 7.853 (4.73), 7.960(3.84), 7.968 (5.02), 7.974 (5.60), 7.981 (6.07), 7.992 (2.28), 8.006(5.09), 8.027 (9.40), 8.048 (3.51), 13.656 (1.36).

Intermediate 1474-[3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-ethyl-1-methyl-1H-pyrazol-5-yl]benzonitrile

A solution of4-[5-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-ethyl-1H-pyrazol-3-yl]benzonitrile(2.00 g, 5.84 mmol) in dimethylformamide (10 ml) was treated with cesiumcarbonate (3.81 g, 11.7 mmol) and iodomethane (1.1 ml, 18 mmol). Themixture was stirred overnight. The mixture was diluted with water andextracted with ethyl acetate (3×). The combined organic phases werewashed with water (2×), brine and dried over sodium sulfate. The crudeproduct was purified using flash-chromatography on silica gel (SNAPUltra 50 g, dichloromethane/ethyl acetate) to obtain 480 mg of thedesired product (23%) together with its regioisomer (650.5 mg, 31%).

LC-MS (method 9): R_(t)=0.98 min; MS (ESIpos): m/z=357 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.811 (7.18), 0.826(16.00), 0.842 (7.14), 1.178 (0.70), 1.992 (1.39), 2.260 (1.84), 2.275(5.58), 2.290 (5.42), 2.305 (1.67), 3.331 (9.52), 7.768 (7.97), 7.772(2.87), 7.782 (3.27), 7.785 (8.91), 7.945 (0.40), 7.948 (0.56), 7.955(5.16), 7.961 (5.42), 7.966 (5.11), 7.972 (7.75), 7.980 (1.11), 8.012(1.01), 8.013 (1.13), 8.021 (8.29), 8.027 (5.63), 8.032 (6.59), 8.037(11.96), 8.046 (1.03), 8.050 (3.10), 8.054 (7.88).

Intermediate 1484-[5-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-ethyl-1-methyl-1H-pyrazol-3-yl]benzonitrile

A solution of4-[5-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-ethyl-1H-pyrazol-3-yl]benzonitrile(2.00 g, 5.84 mmol) in dimethylformamide (10 ml, 130 mmol) was treatedwith cesium carbonate (3.81 g, 11.7 mmol) and iodomethane (1.1 ml, 18mmol). The mixture was stirred overnight. The mixture was diluted withwater and extracted with ethyl acetate (3×). The combined organic phaseswere washed with water (2×), brine and dried over sodium sulfate. Thecrude product was purified using flash-chromatography on silica gel(SNAP Ultra 50 g, dichloromethane/ethyl acetate) to obtain 650.5 mg ofthe desired product (31%) together with its regioisomer (480 mg, 23%).

LC-MS (methd 9): R_(t)=1.03 min; MS (ESIpos): m/z=357 [M+H]⁺

Intermediate 1494-(5-amino-4-ethyl-1-methyl-1H-pyrazol-3-yl)benzonitrile

A solution of4-[5-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-ethyl-1-methyl-1H-pyrazol-3-yl]benzonitrile(643 mg, 1.80 mmol) in ethanol (6.5 ml, 110 mmol) was treated withhydrazine monohydrate (440 9.0 mmol) and stirred at 90° C. overnight.After cooling to ambient temperature the mixture was diluted withsaturated sodium hydrogen carbonate solution and extracted with ethylacetate (3×). The combined organic phases were washed with saturatedsodium hydrogen carbonate solution and brine, dried over sodium sulfateand concentrated under reduced pressure to yield 379 mg (93%) of thedesired product.

LC-MS (method 10): R_(t)=1.29 min; MS (ESIpos): m/z=227 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.010 (1.29), 0.991(5.70), 1.010 (12.56), 1.028 (6.32), 2.460 (1.99), 2.478 (5.79), 3.324(16.00), 5.059 (12.12), 7.726 (5.57), 7.746 (10.37), 7.794 (8.73), 7.814(5.21).

Intermediate 1504-(3-amino-4-ethyl-1-methyl-1H-pyrazol-5-yl)benzonitrile

A solution of4-[3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-ethyl-1-methyl-1H-pyrazol-5-yl]benzonitrile(475 mg, 1.33 mmol) in ethanol (5.0 ml, 86 mmol) was treated withhydrazine monohydrate (320 6.7 mmol) and stirred at 90° C. overnight.After cooling to ambient temperature the mixture was diluted withsaturated sodium hydrogen carbonate solution and extracted with ethylacetate (3×). The combined organic phases were washed with saturatedsodium hydrogen carbonate solution and brine, dried over sodium sulfateand concentrated under reduced pressure to yield 255 mg (83%) of thedesired product.

LC-MS (method 10): R_(t)=1.24 min; MS (ESIpos): m/z=227 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.919 (7.41), 0.937(16.00), 0.956 (7.96), 0.999 (0.66), 2.204 (2.59), 2.222 (7.39), 2.241(7.20), 2.259 (2.43), 3.330 (14.88), 3.506 (0.62), 3.539 (0.73), 3.556(0.43), 4.526 (13.13), 7.544 (8.74), 7.564 (9.27), 7.945 (8.78), 7.965(7.83).

Intermediate 151 4-[cyano(methoxy)acetyl]benzonitrile

A solution of ethyl 4-cyanobenzoate (10.0 g, 57.1 mmol) andmethoxyacetonitrile (8.5 ml, 110 mmol) in tetrahydrofuran (150 ml, 1.8mol) was treated with bis-(trimethylsilyl)-lithiumamid, 1.0 M solutionin tetrahydrofuran (120 ml, 1.0 M, 120 mmol). The mixture was stirredovernight at ambient temperature. The mixture was poured into water andextracted with ethyl acetate. The aqueous phase was acidified withaqueous hydrochloric acid and extracted with dichloromethane (2×). Thecombined organic phases were washed with water, dried over sodiumsulfate and concentrated under reduced pressure to yield 9.20 g of thedesired product (52%).

LC-MS (method 9): R_(t)=0.72 min; MS (ESIneg): m/z=199 [M−H]⁻

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.01), 0.008(1.08), 1.909 (0.77), 2.524 (0.82), 3.246 (1.44), 3.291 (1.02), 3.320(10.48), 3.347 (0.79), 3.353 (0.58), 3.378 (0.70), 3.385 (0.60), 3.401(2.69), 3.451 (0.44), 3.488 (3.57), 3.510 (4.28), 3.565 (12.46), 3.629(0.45), 3.716 (0.62), 3.727 (1.69), 3.757 (0.90), 3.780 (4.13), 3.935(9.19), 4.364 (0.70), 5.081 (0.81), 5.217 (1.07), 6.353 (1.33), 7.746(0.90), 7.762 (3.33), 7.767 (2.22), 7.783 (3.82), 7.810 (11.32), 7.815(4.74), 7.827 (5.10), 7.832 (16.00), 7.925 (3.07), 7.930 (1.44), 7.940(15.74), 7.945 (7.05), 7.957 (4.40), 7.962 (11.09), 7.972 (4.40), 7.989(2.33), 7.994 (6.36), 7.998 (2.80), 8.010 (1.80), 8.020 (1.51), 8.040(0.74), 8.065 (1.96), 8.073 (5.63), 8.078 (2.16), 8.081 (1.54), 8.087(3.66), 8.095 (3.83), 8.113 (1.60), 8.135 (0.62), 8.153 (2.44), 8.175(1.49), 8.653 (1.00), 8.691 (0.86), 8.739 (0.68), 11.168 (4.18), 13.561(0.42).

Intermediate 152 4-(3-amino-4-methoxy-1H-pyrazol-5-yl)benzonitrile

A solution of 4-[cyano(methoxy)acetyl]benzonitrile (9.20 g, 46.0 mmol)in ethanol (340 ml, 5.9 mol) was treated with hydrazine hydrate (1:1)(4.5 ml, 92 mmol) and refluxed for 2 hours. After cooling to ambienttemperature the mixture was diluted with saturated sodium hydrogencarbonate solution. Ethanol was removed under reduced pressure, theremaining was diluted with water and extracted with ethyl acetate (2×).The combined organic phases were washed with brine, dried over sodiumsulfate and concentrated under reduced pressure to yield 5.88 g (58%) ofthe desired product.

LC-MS (method 9): R_(t)=0.56 min; MS (ESIpos): m/z=215 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.175 (0.57), 1.195(0.49), 1.252 (0.54), 1.989 (0.93), 3.196 (0.63), 3.335 (0.54), 3.633(1.24), 3.641 (2.48), 3.666 (16.00), 3.762 (1.92), 4.655 (1.34), 4.906(0.49), 7.414 (0.54), 7.435 (0.57), 7.558 (0.71), 7.580 (0.89), 7.660(0.50), 7.665 (0.41), 7.682 (0.73), 7.687 (0.51), 7.727 (1.01), 7.749(1.07), 7.754 (1.20), 7.771 (0.87), 7.776 (0.96), 7.879 (4.77), 7.909(4.01), 7.928 (3.65), 7.951 (2.99), 7.959 (2.90), 8.008 (0.84), 8.029(0.44), 9.784 (0.51), 11.899 (1.21).

Intermediate 1533-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-5-(4-fluorophenyl)-1-methyl-1H-pyrazole-4-carbaldehyde

A round-bottom flask was charged with3-amino-5-(4-fluorophenyl)-1-methyl-1H-pyrazole-4-carbaldehyde (1.00 g,4.56 mmol) and sodium phenolate (722 mg, 6.22 mmol) and the contentswere suspended in 1,4-dioxane (10 mL). The reaction mixture was degassedwith Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (49.4 mg, 53.9μmol), XantPhos (72.0 mg, 124 μmol) and4-chloro-6-(3,5-dimethylpyrazol-1-yl)pyrimidine (0.865 g, 4.15 mmol)were added and the reaction mixture was degassed again for 1 min. Thevial was sealed and heated at 90° C. overnight while vigorouslystirring. After cooling to ambient temperature, the reaction mixture wasfiltered and concentrated. The residue was dissolved in ethyl acetateand washed with brine. The organic phase phase was dried over magnesiumsulfate, filtered and concentrated. The residue was purified bypreparative SFC (Chiralpak AD SFC 250×20 mm, flow: 80 mL/min, isocraticcarbon dioxide/2-propanol 80/20) to yield the desired product (267 mg,16% yield).

LC-MS (method 10): R_(t)=2.20 min; MS (ESIpos): m/z=392 [M+H]⁺

Intermediate 154 3-oxocyclopent-1-en-1-yl acetate

Under an argon atmosphere, cyclopentane-1,3-dione (18.0 g, 183 mmol) wasdissolved in dichloromethane and pyridine (15 ml, 180 mmol) was added.Acetyl chloride (14 ml, 200 mmol) was slowly added via syringe and thereaction mixture was stirred overnight at ambient temperature. Ice-coldwater was added and the phases were separated. The organic phase phasewas further washed with aqueous hydrochloric acid solution (1 M),saturated aqueous sodium hydrogencarbonate solution and water, driedover sodium sulfate and concentrated. The product thus obtained (23.3 g,90% yield) was used in the next step without further purification.

LC-MS (method 9): R_(t)=0.35 min; MS (ESIpos): m/z=141 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.291 (16.00), 2.351(2.40), 2.356 (1.60), 2.363 (2.48), 2.370 (1.70), 2.375 (2.80), 2.723(1.53), 2.727 (1.96), 2.735 (1.60), 2.740 (1.65), 2.747 (1.69), 2.752(1.42), 6.011 (1.04), 6.015 (2.05), 6.019 (1.18).

Intermediate 155 2-acetylcyclopentane-1,3-dione

Under an argon atmosphere, 3-oxocyclopent-1-en-1-yl acetate (23.3 g, 166mmol) was dissolved in acetonitrile (350 mL) and triethylamine (32 mL,230 mmol) and 2-hydroxy-2-methylpropanenitrile (6.1 mL, 67 mmol) wereadded subsequently and the reaction mixture stirred overnight at ambienttemperature. The reaction mixture was diluted with aqueous hydrochloricacid solution (160 mL, 1 M) and extracted with dichloromethane. Forbetter phase separation, small amounts of Chydrochloric acid₃ wereadded. It was further extracted with dichloromethane and the combinedorganic phase extracts were washed with water, dried over sodium sulfateand concentrated to yield the product (19.2 g, 82% yield) that was usedin the next step without further purification.

LC-MS (method 9): R_(t)=0.23 min; MS (ESIneg): m/z=139 [M−H]⁻

¹H-NMR (400 MHz, CDCl₃) δ [ppm]: 2.512 (0.78), 2.527 (16.00), 2.541(1.08), 2.740 (1.02), 2.755 (1.01), 2.769 (0.70).

Intermediate 1561-(6-chloropyrimidin-4-yl)-3-methyl-5,6-dihydrocyclopenta[c]pyrazol-4(1H)-one

Under an argon atmosphere, 4-chloro-6-hydrazinylpyrimidine (11.3 g, 78.5mmol) and 2-acetylcyclopentane-1,3-dione (10.0 g, 71.4 mmol) weresuspended in ethanol (140 mL) and para-toluenesulfonic acid monohydrate(679 mg, 3.57 mmol) was added. The reaction mixture was stirredovernight at 85° C. bath temperature under slight reflux. After coolingto ambient temperature, it was quenched by addition of saturated aqueoussodium hydrogencarbonate solution and extracted with ethyl acetate (3×).An insoluble solid was filtered off during the extraction and wasdiscarded after further analysis. The combined organic phase extractswere dried over sodium sulfate and concentrated. The residue containingthe two regioisomers was dissolved in methanol/acetonitrile (1:1, 800mL) at 60° C. and purified by preparative SFC (Chiralpak AZ 20μ, 500×400mm, flow 300 mL/min, isocratic gradient carbon dioxide/ethanol 60/40,stacked injection of 18 mL every 25 min) to yield the desired product(5.36 g, 27% yield) along with its regioisomer2-(6-chloropyrimidin-4-yl)-3-methyl-5,6-dihydrocyclopenta[c]pyrazol-4(2H)-one(see below).

LC-MS (method 10): R_(t)=1.08 min; MS (ESIpos): m/z=249 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.47), 0.008(0.45), 2.350 (16.00), 2.394 (1.72), 2.523 (0.48), 2.983 (2.11), 2.989(1.74), 2.996 (2.34), 3.002 (1.84), 3.008 (2.39), 3.368 (2.27), 3.374(1.75), 3.381 (2.20), 3.387 (1.65), 3.393 (1.93), 7.929 (3.50), 9.004(3.30).

Intermediate 1572-(6-chloropyrimidin-4-yl)-3-methyl-5,6-dihydrocyclopenta[c]pyrazol-4(2H)-one

This intermediate was obtained as a regioisomer during the synthesis of1-(6-chloropyrimidin-4-yl)-3-methyl-5,6-dihydrocyclopenta[c]pyrazol-4(1H)-oneand was purified by preparative SFC (Chiralpak AZ 20μ, 500×400 mm, flow300 mL/min, isocratic gradient carbon dioxide/ethanol 60/40, stackedinjection of 18 mL every 25 min) to yield the desired product (2.56 g,13% yield).

LC-MS (method 10): R_(t)=1.10 min; MS (ESIpos): m/z=249 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.845 (16.00), 2.915(0.88), 2.919 (1.00), 2.928 (2.08), 2.933 (1.53), 2.939 (1.58), 2.948(2.90), 2.980 (2.87), 2.995 (1.43), 3.000 (1.79), 3.009 (0.95), 3.162(0.48), 3.175 (0.50), 8.078 (3.79), 9.036 (3.78).

Intermediate 1584-[1-(2-cyclopropylethyl)-3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-methyl-1H-pyrazol-5-yl]benzonitrile

Under an argon atmosphere,4-[3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-methyl-1H-pyrazol-5-yl]benzonitrile(2.00 g, 6.09 mmol) and potassium carbonate (1.68 g, 12 2 mmol) weresuspended in dimethylformamide (8.9 mL) and (2-bromoethyl)cyclopropane(1.3 ml, 12 mmol) was added. The reaction mixture was stirred overnightat ambient temperature. Water was then added and the cloudy solutionfiltered. The oily residue was dissolved in ethyl acetate and washedwith water. The filtrate and the aqeuos phase were combined andextracted with ethyl acetate. The combined organic phase extracts weredried over sodium sulfate and concentrated. The residue was dissolved inmethanol/acetonitrile (50 mL) and purified by preparative SFC (ChiralpakAD-H 5 μm, 250×20 mm, flow: 80 mL/min, isocratic carbondioxide/2-propanol 80/20, injections of 0.8 mL every 20 min) to yieldthe desired product (270 mg, 63% purity, 7% yield) along with itsregioisomer4-[1-(2-cyclopropylethyl)-5-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(see below).

LC-MS (method 14): R_(t)=3.49 min; MS (ESIpos): m/z=397 [M+H]⁺

Intermediate 1594-[3-amino-1-(2-cyclopropylethyl)-4-methyl-1H-pyrazol-5-yl]benzonitrile

4-[1-(2-cyclopropylethyl)-3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-methyl-1H-pyrazol-5-yl]benzonitrile(270 mg, 681 μmol) was dissolved in ethanol (6.4 mL) and hydrazinemonohydrate (170 ∞L, 3.4 mmol) was added. The reaction mixture washeated to reflux for 4 h. After cooling to ambient temperature, it wasdiluted with water and extracted with ethyl acetate. The organic phasewas washed with sat. aqueous sodium hydrogencarbonate and brine anddried over sodium sulfate. The residue was concentrated to yield thedesired product (168 mg, 67% purity, 62% yield) and was used withoutfurther purification.

LC-MS (method 9): R_(t)=0.79 min; MS (ESIpos): m/z=267 [M+H]⁺

Intermediate 1604-[1-(2-cyclopropylethyl)-5-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-methyl-1H-pyrazol-3-yl]benzonitrile

This compound was obtained during the synthesis of its regioisomer4-[1-(2-cyclopropylethyl)-3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-methyl-1H-pyrazol-5-yl]benzonitrile.Separation of the regioisomers by preparative SFC (Chiralpak AD-H 5 μm,250×20 mm, flow: 80 mL/min, isocratic carbon dioxide/2-propanol 80/20,injections of 0.8 mL every 20 min) yielded the title compound (269 mg,11% yield).

LC-MS (method 9): R_(t)=1.15 min; MS (ESIpos): m/z=397 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.061 (0.46), −0.052(1.68), −0.049 (1.57), −0.042 (1.71), −0.031 (0.50), 0.274 (0.51), 0.282(1.42), 0.286 (1.40), 0.291 (0.70), 0.294 (0.69), 0.298 (1.49), 0.301(1.37), 0.310 (0.48), 0.611 (0.51), 1.612 (0.61), 1.626 (1.55), 1.640(1.53), 1.654 (0.59), 2.070 (9.83), 4.071 (1.18), 4.086 (1.87), 4.100(1.14), 7.918 (16.00), 7.981 (1.70), 7.988 (1.72), 7.992 (1.76), 7.998(2.45), 8.058 (2.64), 8.065 (1.82), 8.069 (1.80), 8.075 (1.69).

Intermediate 1614-[5-amino-1-(2-cyclopropylethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile

4-[1-(2-cyclopropylethyl)-5-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(264 mg, 666 μmol) was dissolved in ethanol (10 mL) and hydrazinemonohydrate (160 μL, 3.3 mmol) was added. The reaction mixture washeated to reflux for 4.5 h. After cooling to ambient temperature, theprecipitated solid was removed by filtration. The filtrate wasconcentrated to yield the desired product (209 mg, 57% purity, 67%yield) and was used without further purification.

LC-MS (method 9): R_(t)=0.84 min; MS (ESIpos): m/z=267 [M+H]⁺

Intermediate 1621-(6-{[1-(cyclopropylmethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylicacid

A solution of ethyl1-(6-{[1-(cyclopropylmethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(175 mg, 348 μmol) in tetrahydrofuran (2.5 ml, 31 mmol) was treated withaqueous lithium hydroxide solution (1.7 ml, 1.0 M, 1.7 mmol) and stirredovernight at 80° C. and an additional day at 90° C. After cooling toambient temperature the mixture was diluted with water and extractedonce with ethyl acetate. The organic phase was discarded. The aqueousphase was acidified with hydrochloric acid and extracted with ethylacetate (3×). The combined organic phases were dried over sodium sulfateand concentrated under reduced pressure to yield 71.7 mg (37%) of thedesired product.

LC-MS (method 10): R_(t)=1.95 min; MS (ESIpos): m/z=476 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.49), −0.008(4.42), 0.008 (3.94), 0.146 (0.49), 0.298 (3.16), 0.309 (3.34), 0.437(3.50), 0.456 (3.66), 0.975 (5.18), 0.993 (11.22), 1.012 (5.36), 1.040(1.18), 1.057 (2.36), 1.075 (1.20), 1.175 (0.56), 1.188 (1.00), 1.194(0.99), 1.206 (1.47), 1.218 (0.94), 1.224 (0.99), 1.235 (0.68), 1.910(1.02), 2.357 (11.03), 2.376 (2.32), 2.443 (1.27), 2.461 (2.79), 2.479(2.88), 2.811 (8.97), 2.910 (16.00), 2.931 (0.80), 3.433 (0.70), 3.451(0.68), 3.798 (2.68), 3.814 (2.64), 6.568 (1.44), 7.254 (3.27), 7.276(6.65), 7.298 (3.68), 7.670 (2.01), 7.685 (2.76), 7.703 (1.89), 8.317(1.76), 8.522 (0.57), 9.464 (0.45), 12.627 (0.99).

Intermediate 163

N′-acetyl-1-(6-{[1-(cyclopropylmethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbohydrazide

A solution of1-(6-{[1-(cyclopropylmethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylicacid (68.9 mg, 145 μmol) and acetohydrazide (32.2 mg, 435 μmol) indimethylformamide (1.0 ml, 13 mmol) was treated with HATU (82.6 mg, 217μmol) and N,N-diisopropylethylamine (76 μl, 430 μmol). The mixture wasstirred overnight at ambient temperature. The mixture was diluted withwater and extracted with ethyl acetate (3×). The combined organic phaseswere dried over Extrelut NT3 and concentrated under reduced pressure toyield 95.4 mg (quant.) of the desired product.

LC-MS (method 10): R_(t)=1.65 min; MS (ESIpos): m/z=532 [M+H]⁺

Intermediate 1641-(6-{[4-ethyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylicacid

A solution of ethyl1-(6-{[4-ethyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(177 mg, 383 μmol) in tetrahydrofuran (2.5 ml, 31 mmol) was treated withaqueous lithium hydroxide solution (1.9 ml, 1.0 M, 1.9 mmol) and stirredat 85° C. overbight and additionally one day at 90° C. Afetr cooling toambient temperature the mixture was diluted with water and extractedonce with ethyl acetate. The organic phase was discarded. The aqueousphase was acidified with hydrochloric acid and extracted with ethylacetate (3×). The combined organic phases were dried over sodium sulfateand concentrated under reduced pressure to yield 50.3 mg (30%) of thedesired product.

LC-MS (method 10): R_(t)=1.75 min; MS (ESIpos): m/z=436 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.973 (4.48), 0.991(9.78), 1.010 (4.67), 1.032 (3.19), 1.047 (3.17), 1.910 (0.49), 2.369(3.06), 2.448 (1.13), 2.467 (2.85), 2.486 (3.06), 2.913 (16.00), 3.645(11.42), 7.248 (2.43), 7.270 (5.06), 7.292 (2.88), 7.649 (1.94), 7.664(2.55), 7.669 (2.49), 7.684 (1.88), 8.536 (0.74), 9.519 (0.96), 12.634(1.08).

Intermediate 165N′-acetyl-1-(6-{[4-ethyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbohydrazide

A solution of1-(6-{[4-ethyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylicacid (43.8 mg, 101 μmol) and acetohydrazide (22.4 mg, 302 μmol) indimethylformamide (1.0 ml, 13 mmol) was treated with HATU (57.4 mg, 151μmol) and N,N-diisopropylethylamine (53 μl, 300 μmol). The mixture wasstirred overnight at ambient temperature. The mixture was diluted withwater and extracted with ethyl acetate (3×). The combined organic phaseswere dried over Extrelut NT3 and concentrated under reduced pressure toyield 65.1 mg (quant.) of the desired product

LC-MS (method 10): R_(t)=1.45 min; MS (ESIpos): m/z=492 [M+H]⁺

Intermediate 1664-[1-(2,2-difluoroethyl)-5-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-methyl-1H-pyrazol-3-yl]benzonitrile

A solution of4-[5-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(2.50 g, 7.61 mmol) in dimethylformamide (20 ml, 260 mmol) was treatedwith cesium carbonate (4.96 g, 15.2 mmol) and 2,2-difluoroethyltrifluoromethanesulfonate (2.0 ml, 15 mmol) and was stirred overnight atambient temperature. The mixture was diluted with water and extractedwith ethyl acetate (3×). The combined organic phases were washed withwater, brine, dried over sodium sulfate and concentrated under reducedpressure. The crude product was purified by flash-chromatography onsilica gel (Biotage SNAP Ultra 50 g, dichloromethane/ethyl acetate 40:1)to yield 1.45 g of the desired product (48%) together with itsregioisomer (0.30 g, 10%).

LC-MS (method 10): R_(t)=1.95 min; MS (ESIpos): m/z=393 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.076 (2.67), 2.083(16.00), 4.638 (0.84), 4.646 (0.91), 4.668 (1.69), 4.675 (1.73), 4.697(0.84), 4.704 (0.75), 6.174 (0.57), 6.276 (0.55), 6.283 (1.14), 6.290(0.54), 6.393 (0.50), 7.921 (1.03), 7.923 (0.81), 7.926 (0.60), 7.939(10.08), 7.943 (10.02), 7.955 (0.55), 7.959 (0.76), 7.961 (0.97), 7.973(2.81), 7.979 (2.89), 7.984 (2.73), 7.990 (3.96), 7.998 (0.55), 8.000(0.44), 8.039 (0.47), 8.041 (0.55), 8.049 (4.29), 8.054 (2.90), 8.059(3.03), 8.066 (2.75).

Intermediate 1674-[1-(2,2-difluoroethyl)-3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-methyl-1H-pyrazol-5-yl]benzonitrile

A solution of4-[5-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(2.50 g, 7.61 mmol) in dimethylformamide (20 ml, 260 mmol) was treatedwith cesium carbonate (4.96 g, 15.2 mmol) and 2,2-difluoroethyltrifluoromethanesulfonate (2.0 ml, 15 mmol) and was stirred overnight atambient temperature. The mixture was diluted with water and extractedwith ethyl acetate (3×). The combined organic phases were washed withwater, brine, dried over sodium sulfate and concentrated under reducedpressure. The crude product was purified by flash-chromatography onsilica gel (Biotage SNAP Ultra 50 g, dichloromethane/ethyl acetate 40:1)to yield 300 mg of the desired product (10%) together with itsregioisomer (1.45 g, 48%).

LC-MS (method 10): R_(t)=1.91 min; MS (ESIpos): m/z=393 [M+H]⁺

Intermediate 1684-[5-amino-1-(2,2-difluoroethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile

A solution of4-[1-(2,2-difluoroethyl)-5-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(1.45 g, 3.70 mmol) in ethanol (25 mL) was treated with hydrazinemonohydrate (890 ttl, 18.5 mmol) and stirred at 90° C. overnight. Aftercooling to ambient temperature the mixture was diluted with saturatedsodium hydrogen carbonate solution and extracted with ethyl acetate(3×). The combined organic phases were washed with saturated sodiumhydrogen carbonate solution and brine, dried over sodium sulfate andconcentrated under reduced pressure to yield 950 mg (98%) of the desiredproduct.

LC-MS (method 10): R_(t)=1.43 min; MS (ESIpos): m/z=263 [M+H]⁺

¹H-NMR (600 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.042 (16.00), 3.317(0.88), 4.433 (1.06), 4.440 (1.16), 4.457 (2.17), 4.464 (2.23), 4.481(1.11), 4.488 (1.04), 5.238 (5.93), 6.226 (0.61), 6.311 (0.61), 6.318(1.23), 6.325 (0.63), 6.410 (0.58), 7.796 (2.39), 7.810 (6.51), 7.827(6.45), 7.841 (2.43).

Intermediate 1694-[3-amino-1-(2,2-difluoroethyl)-4-methyl-1H-pyrazol-5-yl]benzonitrile

A solution of4-[1-(2,2-difluoroethyl)-3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-methyl-1H-pyrazol-5-yl]benzonitrile(300 mg, 765 μmol) in ethanol (5 mL) was treated with hydrazinemonohydrate (186 μl, 3.8 mmol) and stirred at 90° C. overnight. Aftercooling to ambient temperature the mixture was diluted with saturatedsodium hydrogen carbonate solution and extracted with ethyl acetate(3×). The combined organic phases were washed with saturated sodiumhydrogen carbonate solution and brine, dried over sodium sulfate andconcentrated under reduced pressure to yield 180 mg (90%) of the desiredproduct.

LC-MS (method 9): R_(t)=0.71 min; MS (ESIpos): m/z=263 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.782 (16.00), 4.094(0.85), 4.105 (0.91), 4.130 (1.75), 4.140 (1.77), 4.166 (0.88), 4.176(0.81), 4.787 (4.36), 6.021 (0.59), 6.150 (0.52), 6.160 (1.19), 6.170(0.54), 6.298 (0.55), 7.528 (3.92), 7.533 (1.43), 7.545 (1.49), 7.549(4.34), 7.961 (4.23), 7.965 (1.44), 7.977 (1.37), 7.982 (3.81).

Intermediate 1701-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazolo[4,3-b]pyridine

Under an argon atmosphere 4,6-dichloropyrimidine (1.15 g, 7.72 mmol),3-methyl-1H-pyrazolo[4,3-b]pyridine (1.03 g, 7.72 mmol) and cesiumcarbonate (2.52 g, 7.72 mmol) were dissolved in dimethylformamide (9.4mL) and stirred at ambient temperature overnight. Water was added to thereaction mixture, which was further stirred for 30 min. The precipitatedsolid was collected by filtration and further washed with water. It wasthen dried overnight under vacuum in a drying-oven to yield the desiredproduct (1.2 g, 63% yield).

LC-MS (method 9): R_(t)=0.91 min; MS (ESIpos): m/z=246 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.660 (16.00), 7.658(1.49), 7.670 (1.55), 7.680 (1.57), 7.691 (1.61), 7.963 (2.08), 8.726(1.66), 8.729 (1.58), 8.737 (1.67), 8.741 (1.53), 8.961 (1.68), 8.963(1.36), 8.982 (1.70), 8.985 (1.42), 8.992 (2.46).

Intermediate 1711-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazolo[4,3-c]pyridine

Under an argon atmosphere, 4,6-dichloropyrimidine (1.12 g, 7.51 mmol),3-methyl-1H-pyrazolo[4,3-c]pyridine (1.00 g, 7.51 mmol) and cesiumcarbonate were suspended in dimethylformamide and the reaction mixturewas stirred overnight at ambient temperature. Water was added to thereaction mixture, which was further stirred for 30 min. The precipitatedsolid was collected by filtration and further washed with water. It wasthen dried overnight under vacuum in a drying-oven to yield the desiredproduct (1.57 g, 85% yield).

LC-MS (method 9): R_(t)=0.63 min; MS (ESIpos): m/z=246 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.997 (0.97), 2.462(2.15), 2.561 (0.93), 2.700 (16.00), 2.733 (0.84), 2.785 (1.45), 2.892(0.71), 3.003 (1.01), 6.892 (0.54), 7.541 (0.53), 7.667 (0.44), 7.963(2.90), 8.516 (1.87), 8.529 (1.84), 8.590 (0.66), 8.616 (0.63), 8.649(0.46), 8.667 (2.81), 8.682 (2.43), 8.941 (0.44), 9.001 (0.43), 9.023(3.18), 9.245 (3.85).

Intermediate 172 4-chloro-6-(3-methyl-1H-pyrazol-1-yl)pyrimidine

Under an argon atmosphere, 4,6-dichloropyrimidine (1.81 g, 12.2 mmol),3-methyl-1H-pyrazole (1.00 g, 12.2 mmol) and cesium carbonate (3.97 g,12.2 mmol) were suspended in dimethylformamide (15 mL) and stirredovernight at ambient temperature. Water was added Water was added to thereaction mixture, which was further stirred for 15 min. The precipitatedsolid was collected by filtration and further washed with water. It wasthen dried overnight under vacuum in a drying-oven at 40° C. to yieldthe desired product (1.58 g, 63% yield).

LC-MS (method 10): R_(t)=1.66 min; MS (ESIpos): m/z=195 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.316 (16.00), 2.343(0.21), 2.711 (1.18), 6.445 (0.25), 6.525 (2.49), 6.531 (2.60), 7.817(0.25), 7.857 (3.22), 7.988 (0.26), 8.569 (2.22), 8.575 (2.46), 8.905(3.20), 8.957 (0.27).

Intermediate 173 4-chloro-6-(1H-pyrazol-1-yl)pyrimidine

Under an argon atmosphere, 1H-pyrazole (1.00 g, 14.7 mmol),4,6-dichloropyrimidine (2.19 g, 14.7 mmol) and cesium carbonate (4.79 g,14.7 mmol) were suspended in dimethylformamide (18 mL) and stirredovernight at ambient temperature. Water was added Water was added to thereaction mixture, which was further stirred for 15 min. The precipitatedsolid was collected by filtration and further washed with water. It wasthen dried overnight under vacuum in a drying-oven at 40° C. to yieldthe desired product (2.02 g, 76% yield).

LC-MS (method 10): R_(t)=1.45 min; MS (ESIpos): m/z=181 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 6.705 (9.36), 6.710(12.76), 6.715 (10.30), 7.978 (16.00), 8.011 (13.25), 8.254 (0.76),8.705 (12.40), 8.711 (13.01), 8.735 (1.17), 8.742 (1.18), 8.964 (12.88),8.988 (0.71).

Intermediate 1744-chloro-6-[4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidine

Under an argon atmosphere, 4-(trifluoromethyl)-1H-pyrazole (1.13 g, 8.27mmol), 4,6-dichloropyrimidine (1.23 g, 8.27 mmol) and cesium carbonate(2.69 g, 8.27 mmol) were suspended in dimethylformamide (10 mL) andstirred overnight at ambient temperature. Water was added to thereaction mixture, which was further stirred for 15 min. Filtration ofthe cloudy mixture was not possible, therefore the mixture was dilutedwith brine and extracted with ethyl acetate (3×). The combined organicphase extracts were washed with brine, dried over sodium sulfate andconcentrated. The desired product thus obtained (1.6 g, 62% purity, 46%yield) was used in the next step without further purification.

LC-MS (method 11): R_(t)=1.33 min; MS (ESIpos): m/z=249 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.66), −0.008(4.89), 0.008 (5.43), 0.146 (0.66), 2.329 (0.83), 2.367 (1.03), 2.671(0.94), 2.711 (1.09), 2.732 (8.86), 2.892 (11.86), 7.953 (1.20), 8.103(16.00), 8.345 (8.23), 8.482 (14.11), 8.510 (15.23), 8.965 (0.51), 9.060(12.11), 9.157 (5.91), 9.159 (6.71), 9.362 (12.20), 9.406 (11.77).

Intermediate 175 3-(4-bromophenyl)-2-methyl-3-oxopropanenitrile

Under an argon atmosphere, ethyl 4-bromobenzoate (7.1 ml, 44 mmol) andpropanenitrile (4.4 ml, 61 mmol) were dissolved in tetrahydrofuran (100mL) and a solution of lithium bis(trimethylsilyl)amide (63 ml, 1.0 M, 63mmol) was added dropwise at ambient temperature. The reaction mixturewas stirred for 2 h, and no further conversion took place. Furtheraliquots of propanenitrile (1.1 ml, 15 mmol) and lithiumbis(trimethylsilyl)amide solution (17 ml, 1.0 M, 17 mmol) were thenadded and the reaction mixture allowed to stir overnight. The reactionwas quenched by addition of water and extracted with dichloromethane.The organic phase was discarded. The aqueous phase was acidified withaqueous hydrochloric acid to pH1-2 and extracted with dichloromethane(3×). The combined organic phase extracts were dried over sodium sulfateand concentrated. The desired product thus obtained (9.17 g, 85% purity,75% yield) was used in the next step without further purification.

LC-MS (method 10): R_(t)=1.73 min; MS (ESIneg): m/z=236 [M−H]⁻

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.92), 1.458(10.79), 1.476 (10.91), 1.664 (3.23), 1.854 (16.00), 5.098 (0.89), 5.116(2.71), 5.134 (2.69), 5.152 (0.89), 7.359 (0.77), 7.380 (0.93), 7.484(4.07), 7.505 (5.05), 7.674 (5.46), 7.695 (4.62), 7.812 (4.67), 7.833(6.58), 7.937 (6.71), 7.959 (4.93), 10.936 (1.03).

Intermediate 176 3-(4-bromophenyl)-1,4-dimethyl-1H-pyrazol-5-amine

3-(4-bromophenyl)-2-methyl-3-oxopropanenitrile (6.00 g, 25.2 mmol) wasdissolved in toluene (100 mL) and methylhydrazine (1.3 ml, 25 mmol) andacetic acid (1.4 ml, 25 mmol) were added subsequently. The reactionmixture was stirred overnight at ambient temperature. The solvent wasremoved under reduced pressure and the residue redissolved indichloromethane. It was loaded onto celite and purified by flash columnchromatography (SNAP Ultra 100 g, cyclohexane/ethyl acetate gradient60/40 to 0:100) to yield the desired product (5.56 g, 83% yield) alongwith its regioisomer (0.53 g, 8%).

LC-MS (method 9): R_(t)=0.70 min; MS (ESIpos): m/z=266 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.99 (s, 3H), 3.57 (s,3H), 4.98 (s, 2H), 7.54 (m, 4H).

Intermediate 1771-[1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]ethanone

A solution of 4,6-dichloropyrimidine (1.08 g, 7.24 mmol) and1-(3,5-dimethyl-1H-pyrazol-4-yl)ethanone (1.00 g, 7.24 mmol) indimethylformamide (5.0 ml) was treated with cesium carbonate (2.36 g,7.24 mmol) and stirred 1.5 hours at ambient temperature. The mixture wasdiluted with water; the occurring precipitate was collected byfiltration, washed with water and dried to yield 1.40 g (74%) of thedesired product.

LC-MS (method 10): R_(t)=1.74 min; MS (ESIpos): m/z=251 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.461 (15.85), 2.922(16.00), 2.968 (1.34), 7.990 (2.95), 9.014 (3.30).

Intermediate 1781-[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]ethanone

A microwave vial was charged1-[1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]ethanone (530mg, 2.11 mmol) and1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine(570 mg, 2.33 mmol) and the contents were suspended in 1,4-dioxane (8.6ml, 100 mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (58.1 mg, 63.4 μmol) and Xantphos(73.4 mg, 127 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (270 mg, 2.33 mmol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with brine andextracted with ethyl acetate (2×). The combined organic phases weredried over sodium sulfate and concentrated under reduced pressure. Thecrude product was purified by preparative HPLC (method: column: ReprosilC18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent: A=water (0.01% formicacid), B=acetonitrile/gradient: 0.00-5.00 min=10% B, 6.50 min=20% B,17.0-19.75 min=100% B, 19.75-23.00 min=90% B) to yield the desiredproduct (305 mg, 26%).

LC-MS (method 11): R_(t)=1.41 min; MS (ESIpos): m/z=460 [M+H]+

Intermediate 179 3-(4-fluorophenyl)-2-methoxy-3-oxopropanenitrile

A solution of ethyl 4-fluorobenzoate (4.4 ml, 30 mmol) intetrahydrofuran (88 ml, 1.1 mol) was treated with lithiumbis(trimethylsilyl)amide (62 ml, 1.0 M in tetrahydrofuran, 62 mmol). Themixture was stirred overnight at ambient temperature. The mixture wasdiluted with water and extracted with dichloromethane. The organic phasewas discarded. The aqueous phase was acidified with hydrochloric acidand extracted with dichloromethane (2×). The combined organic phaseswere washed with water, dried over sodium sulfate and concentrated underreduced pressure to yield 10.0 g (80%) of the desired product.

LC-MS (method 10): R_(t)=1.54 min; MS (ESIneg): m/z=192 [M−H]⁻

Intermediate 180 3-(4-fluorophenyl)-4-methoxy-1H-pyrazol-5-amine

A solution of 3-(4-fluorophenyl)-2-methoxy-3-oxopropanenitrile (4.50 g,23 3 mmol) in ethanol (40 ml, 690 mmol) was treated with hydrazinehydrate (1:1) (2.3 ml, 47 mmol) and refluxed overnight. After cooling toambient temperature the mixture was poured into ice water. Saturatedsodium hydrogen carbonate solution was added and the mixture wasextracted with ethyl acetate. The combined organic phases were washedwith brine, dried over sodium sulfate and concentrated under reducedpressure to yield 2.70 g (39%) of the desired product.

LC-MS (method 10): R_(t)=1.07 min; MS (ESIpos): m/z=208 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.281 (0.58), 1.355(0.48), 1.719 (0.83), 1.785 (0.65), 1.842 (1.35), 1.857 (0.83), 1.880(0.56), 1.911 (0.41), 1.931 (4.34), 1.937 (3.87), 1.957 (4.21), 1.972(4.40), 1.986 (1.87), 2.004 (4.19), 2.019 (0.65), 2.074 (0.68), 2.086(2.74), 2.168 (0.51), 3.600 (1.14), 3.610 (1.45), 3.631 (16.00), 4.591(0.85), 7.234 (1.77), 7.256 (3.38), 7.270 (1.65), 7.278 (2.23), 7.303(0.95), 7.411 (0.64), 7.425 (0.74), 7.432 (0.63), 7.447 (0.50), 7.755(1.85), 7.769 (2.22), 7.776 (2.12), 7.790 (1.71), 10.430 (1.00).

Intermediate 1812-[3-(4-fluorophenyl)-4-methoxy-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione

A solution of 3-(4-fluorophenyl)-4-methoxy-1H-pyrazol-5-amine (1.94 g,90% purity, 8.43 mmol) and 2-benzofuran-1,3-dione (1.87 g, 12.6 mmol) inacetic acid (17 ml) was stirred overnight at 125° C. After cooling toambient temperature, acetic acid was removed under reduced pressure. Theremaining residue was diluted with water and extracted with ethylacetate. The combined organic phases were washed with water, brine,dried over sodium sulfate and concentrated under reduced pressure. Thecrude product was purified by flash-chromatography on silica gel(column: Biotage Snap Ultra 50 g, solvent: dichloromethane/ethyl acetate10:1) to yield 1.60 g of the desired product (56%).

LC-MS (method 10): R_(t)=1.73 min; MS (ESIpos): m/z=338 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.008 (0.43), 2.074(3.12), 3.607 (16.00), 7.363 (1.99), 7.385 (3.78), 7.408 (1.95), 7.823(2.29), 7.837 (2.63), 7.845 (2.34), 7.859 (1.96), 7.965 (2.39), 7.973(2.85), 7.978 (2.92), 7.986 (3.87), 7.996 (1.03), 8.022 (0.96), 8.032(3.74), 8.040 (2.70), 8.046 (2.47), 8.054 (2.02), 13.484 (2.62).

Intermediate 1822-[3-(4-fluorophenyl)-4-methoxy-1-methyl-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione

A solution of2-[3-(4-fluorophenyl)-4-methoxy-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(1.58 g, 4.68 mmol) in dimethylformamide (15 ml, 200 mmol) was treatedwith cesium carbonate (3.05 g, 9.37 mmol) and iodomethane (580 μl, 9.4mmol). The mixture was stirred overnight. The mixture was diluted withwater and extracted with ethyl acetate (3×). The combined organic phaseswere washed with water (2×), brine and dried over sodium sulfate. Thecrude product was purified using flash-chromatography on silica gel(SNAP Ultra 10 g, dichloromethane/ethyl acetate 40:1) to obtain 84 mg ofthe desired product (5%) together with its regioisomer (105 mg, 6%).

LC-MS (method 10) R_(t)=1.99 min; MS (ESIpos): m/z=352 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.279 (0.43), 3.610(16.00), 3.711 (13.88), 3.818 (1.03), 3.822 (1.27), 3.945 (0.44), 7.271(1.59), 7.293 (3.32), 7.315 (1.81), 7.864 (1.87), 7.878 (2.15), 7.886(2.14), 7.900 (1.81), 7.992 (1.84), 8.000 (2.09), 8.006 (2.24), 8.014(2.97), 8.025 (0.53), 8.065 (0.50), 8.075 (2.95), 8.083 (2.17), 8.089(2.09), 8.097 (1.80).

Intermediate 1832-[5-(4-fluorophenyl)-4-methoxy-1-methyl-1H-pyrazol-3-yl]-1H-isoindole-1,3(2H)-dione

A solution of2-[3-(4-fluorophenyl)-4-methoxy-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione (1.58 g, 4.68 mmol) in dimethylformamide (15 ml, 200 mmol)was treated with cesium carbonate (3.05 g, 9.37 mmol) and iodomethane(580 μl, 9.4 mmol). The mixture was stirred overnight. The mixture wasdiluted with water and extracted with ethyl acetate (3×). The combinedorganic phases were washed with water (2×), brine and dried over sodiumsulfate. The crude product was purified using flash-chromatography onsilica gel (SNAP Ultra 10 g, dichloromethane/ethyl acetate 40:1) toobtain 105 mg of the desired product (6%) together with its regioisomer(84 mg, 5%).

LC-MS (method 10): R_(t)=1.83 min; MS (ESIpos): m/z=352 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.073 (0.54), 3.469(16.00), 3.789 (13.18), 7.386 (1.50), 7.408 (3.04), 7.430 (1.63), 7.643(1.88), 7.657 (2.27), 7.662 (1.97), 7.678 (1.51), 7.958 (1.62), 7.966(2.19), 7.971 (2.13), 7.979 (2.75), 8.014 (0.60), 8.025 (2.90), 8.032(2.17), 8.039 (1.88), 8.046 (1.52).

Intermediate 1843-(4-fluorophenyl)-4-methoxy-1-methyl-1H-pyrazol-5-amine

A solution of2-[3-(4-fluorophenyl)-4-methoxy-1-methyl-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(84.0 mg, 239 μmol) in ethanol (2 mL) was treated with hydrazinemonohydrate (58 μl, 1.2 mmol) and stirred at 90° C. overnight. Aftercooling to ambient temperature the mixture was diluted with water andextracted with ethyl acetate (3×). The combined organic phases werewashed with 1M sodium hydrogen carbonate solution and brine, dried oversodium sulfate and concentrated under reduced pressure to yield 51.0 mg(75%) of the desired product.

LC-MS (method 11): R_(t)=0.91 min; MS (ESIpos): m/z=222 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.72), 0.008(0.69), 1.091 (0.48), 3.537 (14.59), 3.597 (16.00), 5.037 (3.62), 7.165(1.74), 7.170 (0.65), 7.182 (0.83), 7.188 (3.65), 7.193 (0.83), 7.205(0.67), 7.210 (1.95), 7.785 (1.81), 7.791 (0.77), 7.799 (2.02), 7.808(2.01), 7.816 (0.75), 7.822 (1.78).

Intermediate 1855-(4-fluorophenyl)-4-methoxy-1-methyl-1H-pyrazol-3-amine

A solution of2-[5-(4-fluorophenyl)-4-methoxy-1-methyl-1H-pyrazol-3-yl]-1H-isoindole-1,3(2H)-dione (105 mg, 299 μmol) in ethanol (2.6 mL) was treated withhydrazine monohydrate (73 μl, 1.5 mmol) and stirred at 90° C. overnight.After cooling to ambient temperature the mixture was diluted with waterand extracted with ethyl acetate (3×). The combined organic phases werewashed with 1M sodium hydrogen carbonate solution and brine, dried oversodium sulfate and concentrated under reduced pressure to yield 67.0 mg(66%) of the desired product.

LC-MS (method 11): R_(t)=0.92 min; MS (ESIpos): m/z=222 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.714 (0.45), 3.331(1.36), 3.471 (16.00), 4.539 (1.96), 7.310 (1.83), 7.313 (0.89), 7.327(3.96), 7.341 (0.96), 7.345 (2.28), 7.476 (2.26), 7.481 (1.24), 7.488(2.58), 7.494 (2.29), 7.501 (1.07), 7.505 (1.90).

Intermediate 186 ethyl[1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]acetate

A solution of 4-chloro-6-hydrazinylpyrimidine (5.00 g, 34.6 mmol) inethanol (70 ml, 1.2 mol) was treated with ethyl 3-acetyl-4-oxopentanoate(6.44 g, 34.6 mmol) and refluxed overnight. After cooling to roomtemperature the precipitate was collected by filtration, washed withethanol and dried to yield 5.84 g (57%) of the desired product.

LC-MS (method 10): R_(t)=1.99 min; MS (ESIpos): m/z=295 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.171 (4.91), 1.188(10.15), 1.206 (5.04), 2.189 (16.00), 2.611 (14.69), 3.383 (1.43), 3.430(0.76), 3.449 (0.62), 4.058 (1.62), 4.076 (4.86), 4.094 (4.79), 4.112(1.56), 7.898 (3.18), 8.897 (3.57).

Intermediate 187 ethyl1-(6-{[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate

A microwave vial was charged with5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-amine (84.0 mg, 409 μmol),ethyl 1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate (120mg, 450 μmol) and sodium phenolate (52.2 mg, 450 μmol) and the contentswere suspended in 1,4-dioxane (1.2 mL). The reaction mixture wasdegassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (4.87mg, 5.32 ttmol) and XantPhos (7.10 mg, 12.3 μmol) were added and thereaction mixture was degassed again for 1 min. The vial was sealed andheated at 85° C. overnight while vigorously shaking. After cooling toambient temperature, the reaction mixture was filtered and concentrated.The residue was redissolved in dimethylsulfoxide and purified bypreparative HPLC (method 3) to yield the desired product (7.8 mg, 4%yield).

LC-MS (method 10): R_(t)=2.00 min; MS (ESIpos): m/z=436 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.08), 0.008(1.23), 1.196 (4.83), 1.214 (10.43), 1.232 (5.08), 1.866 (11.62), 2.274(14.25), 2.327 (0.62), 2.670 (0.68), 3.691 (16.00), 4.239 (1.55), 4.257(4.87), 4.275 (4.83), 4.292 (1.47), 6.751 (4.70), 7.312 (0.91), 7.358(2.02), 7.380 (4.55), 7.402 (2.66), 7.515 (2.53), 7.521 (1.13), 7.529(2.83), 7.537 (2.30), 7.546 (0.91), 7.551 (1.94), 8.417 (2.60), 9.630(1.74).

Intermediate 188 ethyl1-(6-{[4-ethyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate

A microwave vial was charged with4-ethyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-amine (89.7 mg, 409μmol), ethyl1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate (120 mg,450 μmol) and sodium phenolate (52.2 mg, 450 μmol) and the contents weresuspended in 1,4-dioxane (1.2 mL). The reaction mixture was degassedwith Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (4.87 mg, 5.32μmol) and XantPhos (7.10 mg, 12.3 μmol) were added and the reactionmixture was degassed again for 1 min. The vial was sealed and heated at85° C. overnight while vigorously shaking. After cooling to ambienttemperature, the reaction mixture was filtered and concentrated. Theresidue was redissolved in dimethylsulfoxide and purified by preparativeHPLC (method 3) to yield the desired product (42 mg, 80% purity, 18%yield).

LC-MS (method 10): R_(t)=2.04 min; MS (ESIpos): m/z=450 [M+H]⁺

Intermediate 1894-chloro-6-(4-fluoro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine

4,6-dichloropyrimidine (1.28 g, 8.59 mmol),4-fluoro-3,5-dimethyl-1H-pyrazole (980 mg, 8.59 mmol) and cesiumcarbonate (2.80 g, 8.59 mmol) were suspended in dimethylformamide (5.1mL) and stirred at ambient temperature overnight. Water was then addedand the reaction mixture further stirred for 15 min. The precipitatedsolid was collected by filtration, washed with water and dried in adrying-oven overnight at 40° C. The desired product thus obtained (1.55g, 74% yield) was used in the next step without further purification.

LC-MS (method 11): Rt=1.41 min; MS (ESIpos): m/z=227 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.54), 0.008(0.45), 2.263 (16.00), 2.282 (0.55), 2.617 (9.61), 2.622 (7.84), 2.646(0.32), 2.673 (1.24), 7.894 (2.73), 7.923 (0.23), 8.914 (3.27), 8.948(0.28).

Intermediate 1902-methyl-3-oxo-3-[4-(trifluoromethoxy)phenyl]propanenitrile

Under an argon atmosphere, ethyl 4-(trifluoromethoxy)benzoate (8.00 g,34.2 mmol) and propanenitrile (3.7 ml, 51 mmol) were dissolved intetrahydrofuran (60 mL) and the resulting solution chilled with a waterbath. A solution of lithium bis(trimethylsilyl)amide (53 ml, 1.0 M, 53mmol) was added slowly and the reaction mixture stirred at ambienttemperature for 2 h. Water was added and the mixture extracted withethyl acetate. The organic phase was discarded and the aqueous phaseacidified with aqueous hydrochloric acid solution (1.0 M). The acidicaqueous phase was extracted with ethyl acetate (3×) and the combinedorganic phase extracts were washed with brine, dried over sodium sulfateand concentrated. The desired product thus obtained (6.21 g, 74% yield)was used in the next step without further purification.

LC-MS (method 11): R_(t)=1.27 min; MS (ESIpos): m/z=244 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.008 (0.62), 1.474(8.85), 1.492 (8.96), 1.668 (3.23), 1.837 (1.43), 1.870 (16.00), 1.910(2.16), 5.129 (0.74), 5.147 (2.20), 5.165 (2.18), 5.183 (0.71), 7.470(3.36), 7.491 (4.29), 7.553 (1.29), 7.575 (3.87), 7.597 (3.51), 7.672(4.95), 7.694 (4.07), 8.040 (0.20), 8.055 (0.17), 8.077 (0.19), 8.151(4.90), 8.173 (4.57), 8.282 (0.38), 8.305 (0.34), 10.971 (0.88).

Intermediate 1911-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-5-amine

2-methyl-3-oxo-3-[4-(trifluoromethoxy)phenyl]propanenitrile (3.00 g,12.3 mmol) and (cyclopropylmethyl)hydrazine dihydrochloride (2.45 g,15.4 mmol) were suspended in 2-propanol (25 mL) and the reaction mixturewas stirred under reflux for 3 h. After cooling to ambient temperature,it was concentrated to ⅓ of its original volume and aqueous saturatedsodium hydrogencarbonate solution was added carefully. The reactionmixture was extracted with ethyl acetate (3×) and the combined organicphase extracts were washed with brine, dried over sodium sulfate andconcentrated. The desired product thus obtained was used in the nextstep without further purification (3.66 g, 92% yield).

LC-MS (method 10): R_(t)=1.86 min; MS (ESIpos): m/z=312 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.008 (0.62), 1.474(8.85), 1.492 (8.96), 1.668 (3.23), 1.837 (1.43), 1.870 (16.00), 1.910(2.16), 5.129 (0.74), 5.147 (2.20), 5.165 (2.18), 5.183 (0.71), 7.470(3.36), 7.491 (4.29), 7.553 (1.29), 7.575 (3.87), 7.597 (3.51), 7.672(4.95), 7.694 (4.07), 8.040 (0.20), 8.055 (0.17), 8.077 (0.19), 8.151(4.90), 8.173 (4.57), 8.282 (0.38), 8.305 (0.34), 10.971 (0.88).

Intermediate 1922-methyl-3-oxo-3-[4-(trifluoromethyl)phenyl]propanenitrile

Under an argon atmosphere, ethyl 4-(trifluoromethyl)benzoate (3.32 g,15.2 mmol) and propanenitrile (1.6 ml, 23 mmol) were dissolved intetrahydrofuran (30 mL) and the resulting solution chilled with a waterbath. A solution of lithium bis(trimethylsilyl)amide (24 ml, 1.0 M, 24mmol) was added slowly and the reaction mixture stirred at ambienttemperature for 2 h. Water was added and the mixture extracted withethyl acetate. The organic phase was discarded and the aqueous phaseacidified with aqueous hydrochloric acid solution (1.0 M). The acidicaqueous phase was extracted with ethyl acetate (3×) and the combinedorganic phase extracts were washed with brine, dried over sodium sulfateand concentrated. The desired product thus obtained (6.21 g, 74% yield)was used in the next step without further purification.

LC-MS (method 11): R_(t)=1.24 min; MS (ESIpos): m/z=228 [M+H]⁺

H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.008 (0.30), 1.175(0.24), 1.482 (2.73), 1.500 (2.76), 1.672 (2.76), 1.849 (0.22), 1.892(16.00), 1.909 (2.06), 1.989 (0.45), 5.179 (0.24), 5.196 (0.69), 5.214(0.68), 5.232 (0.24), 7.639 (0.48), 7.659 (0.58), 7.758 (2.82), 7.779(4.37), 7.846 (4.69), 7.867 (3.09), 7.971 (1.26), 7.991 (1.47), 8.200(1.45), 8.220 (1.22), 11.103 (0.63).

Intermediate 1931-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethyl)phenyl]-1H-pyrazol-5-amine

2-methyl-3-oxo-3-[4-(trifluoromethyl)phenyl]propanenitrile (1.20 g, 5.28mmol) and (cyclopropylmethyl)hydrazine dihydrochloride (1.05 g, 6.60mmol) were suspended in 2-propanol (12 mL) and the reaction mixture wasstirred under reflux for 3 h. After cooling to ambient temperature,aqueous saturated sodium hydrogencarbonate solution was added carefully.The reaction mixture was extracted with ethyl acetate (3×) and thecombined organic phase extracts were washed with brine, dried oversodium sulfate and concentrated. The desired product thus obtained wasused in the next step without further purification (1.52 g, 90% purity,87% yield).

LC-MS (method 10): R_(t)=1.84 min; MS (ESIpos): m/z=296 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.347 (0.66), 0.360(2.54), 0.363 (2.53), 0.372 (2.96), 0.384 (1.01), 0.407 (0.39), 0.427(1.08), 0.435 (2.29), 0.446 (1.55), 0.455 (2.50), 0.471 (0.56), 1.175(0.19), 1.194 (0.45), 1.205 (0.67), 1.212 (0.60), 1.224 (0.90), 1.236(0.63), 1.242 (0.58), 1.254 (0.29), 1.337 (0.22), 1.352 (0.22), 1.693(0.27), 1.780 (0.18), 1.825 (0.18), 1.990 (0.16), 2.024 (1.18), 2.038(16.00), 2.135 (0.49), 2.432 (0.46), 3.830 (4.46), 3.847 (4.35), 5.006(1.95), 7.705 (2.76), 7.726 (3.96), 7.771 (0.98), 7.808 (4.09), 7.828(2.80), 7.847 (0.28), 7.868 (0.18), 7.892 (0.19), 7.905 (0.19), 8.155(0.17).

Intermediate 1944-chloro-6-[5-methyl-3-(propan-2-yl)-1H-pyrazol-1-yl]pyrimidine

4,6-Dichloropyrimidine (1.08 g, 7.25 mmol),5-methyl-3-(propan-2-yl)-1H-pyrazole (900 mg, 7.25 mmol) and cesiumcarbonate (2.36 g, 7.25 mmol) were suspended in dimethylformamide (8.8mL) and the reaction mixture was stirred overnight at ambienttemperature. A second batch of 4,6-dichloropyrimidine (1.08 g, 7.25mmol) was added and the reaction mixture stirred again overnight. Waterwas added and the the precipitated solid was collected by filtration.The solid was purified by flash column chromatography (SNAP Ultra 25 g,cyclohexane/ethyl acetate gradient, then wash withdichloromethane/methanol 80/20) to yield a mixture of both isomers. Thetwo regioisomers were separated by preparative HPLC (Daicel ChiralpakAS-H 5 μm, 250×20 mm, Flow: 20 mL/min, injections of 30 μL every 7 min,n-heptane/ethanol isocratic 99.5/0.5) to yield the desired product (104mg, 6% yield).

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.223 (15.72), 1.241(16.00), 2.671 (9.29), 2.673 (9.86), 2.909 (0.92), 2.927 (1.22), 2.944(0.89), 6.353 (2.45), 7.897 (2.74), 7.900 (2.95), 8.899 (2.44), 8.901(2.61).

Intermediate 195 ethyl4-chloro-1-[6-({1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3-methyl-1H-pyrazole-5-carboxylate

Under an argon atmosphere,1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-5-amine(314 mg, 1.01 mmol) was dissolved in 1,4-dioxane (2.2 mL) and sodiumphenolate (117 mg, 1.01 mmol) was added. The reaction mixture wasdegassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (10.9mg, 11.9 μmol), XantPhos (15.9 mg, 27.5 μmol) and ethyl4-chloro-1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate(368 mg, 75% purity, 917 itmol) were added and the reaction mixture wasdegassed again for 1 min. It was then heated at 90° C. overnight whilevigorously stirring. After cooling to ambient temperature, the reactionmixture was loaded on silica gel and purified by flash columnchromatography (SNAP Ultra 25 g, cyclohexane/ethyl acetate gradient 95/5to 20/80) to yield the desired product (176 mg, 80% purity, 27% yield).

LC-MS (method 10) R_(t)=2.59 min; MS (ESIpos): m/z=576 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.26), −0.008(2.04), 0.008 (2.25), 0.146 (0.30), 0.299 (2.85), 0.346 (0.58), 0.358(0.60), 0.423 (3.10), 0.442 (3.60), 1.158 (0.60), 1.175 (1.08), 1.190(1.53), 1.207 (1.45), 1.231 (6.00), 1.249 (11.55), 1.267 (5.92), 1.315(0.68), 1.363 (0.45), 1.380 (0.27), 1.398 (7.00), 1.428 (0.36), 1.965(0.21), 1.989 (0.44), 2.000 (2.88), 2.036 (16.00), 2.130 (0.25), 2.147(0.26), 2.177 (0.26), 2.271 (2.19), 2.328 (0.97), 2.333 (0.84), 2.367(0.38), 2.375 (0.53), 2.394 (0.23), 2.680 (1.63), 2.711 (0.40), 3.568(0.48), 3.802 (0.79), 3.819 (0.93), 3.851 (2.49), 3.866 (2.49), 4.329(2.26), 4.347 (6.84), 4.364 (6.82), 4.382 (2.38), 4.948 (0.84), 7.171(0.22), 7.342 (0.53), 7.363 (0.60), 7.429 (3.89), 7.450 (4.32), 7.684(0.79), 7.706 (0.75), 7.827 (2.51), 7.843 (1.99), 8.433 (0.32), 9.625(0.30).

Intermediate 196 ethyl1-[6-({1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3-methyl-1H-pyrazole-5-carboxylate

Under an argon atmosphere,1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-5-amine(314 mg, 1.01 mmol) was dissolved in 1,4-dioxane (2.2 mL) and sodiumphenolate (117 mg, 1.01 mmol) was added. The reaction mixture wasdegassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (10.9mg, 11.9 μmol), XantPhos (15.9 mg, 27.5 μmol) and ethyl1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate (272 mg,90% purity, 917 μmol) were added and the reaction mixture was degassedagain for 1 min. It was then heated at 90° C. overnight while vigorouslystirring. After cooling to ambient temperature, the reaction mixture wasloaded on silica gel and purified by flash column chromatography (SNAPUltra 25 g, cyclohexane/ethyl acetate gradient 95/5 to 20/80) andfurther purified by preparative HPLC (column: Chromatorex C18; 125*30mm, 10 μM, flow 75 mL/min, gradient acetonitrile/water (containing 0.1%trifluoroacetic acid) 5/95 to 95/5) to yield the desired product (114mg, 23% yield).

LC-MS (method 9): R_(t)=1.25 min; MS (ESIpos): m/z=542 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.20), −0.022(0.38), 0.008 (1.64), 0.146 (0.20), 0.293 (2.56), 0.303 (2.73), 0.426(2.85), 0.445 (2.98), 1.164 (0.44), 1.176 (0.82), 1.200 (6.83), 1.218(13.27), 1.235 (7.16), 2.042 (16.00), 2.261 (2.83), 2.328 (0.42), 2.367(0.28), 2.670 (0.30), 2.711 (0.24), 3.854 (2.58), 3.870 (2.53), 4.246(2.10), 4.264 (6.63), 4.282 (6.57), 4.300 (2.06), 6.750 (2.03), 7.429(3.68), 7.450 (4.07), 7.826 (2.65), 7.847 (2.47), 8.434 (0.44), 9.582(0.36).

Intermediate 197N′-acetyl-1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbohydrazide

A solution of1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylicacid (66.0 mg, 152 μmol) and acetohydrazide (33.7 mg, 455 μmol) indimethylformamide (1.0 ml, 13 mmol) was treated with HATU (86.4 mg, 227μmol) and N,N-diisopropylethylamine (79 450 μmol) ans stirred overnightat ambient temperature. The mixture was purified using preparative HPLC(method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent:A=water (0.01% formic acid), B=acetonitrile/gradient: 0.00-5.00 min=10%B, 6.50 min=20% B, 17.0-19.75 min=100% B, 19.75-23.00min=90% B) to yield58.0 mg of the desired product (78%).

LC-MS (method 10): R_(t)=1.46 min; MS (ESIpos): m/z=492 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.43), 0.008(1.20), 0.873 (3.58), 0.892 (8.13), 0.911 (3.70), 1.141 (0.68), 1.882(1.12), 1.905 (11.25), 2.299 (11.74), 2.309 (2.88), 2.328 (2.71), 2.346(0.76), 2.524 (0.59), 2.756 (12.15), 3.652 (16.00), 7.359 (2.13), 7.364(1.10), 7.376 (2.54), 7.381 (5.24), 7.398 (0.96), 7.403 (2.68), 7.503(2.56), 7.508 (1.12), 7.516 (2.86), 7.524 (2.25), 7.533 (0.89), 7.538(1.88), 8.500 (2.43), 9.471 (1.54), 9.701 (2.34), 9.886 (2.71).

Intermediate 1981-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbaldehyde

A solution of[1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]methanol(135 mg, 320 μmol) in dichloromethane (5.0 ml, 78 mmol) was treated withmanganese(IV) oxide (139 mg, 1.60 mmol). The mixture was stirred onehour at ambient temperature and left over the weekend. Additional fiveequivalents of manganese(IV) oxide (139.2 mg, 1.6 mmol) were added atthe mixture was again stirred overnight and 4 days at ambienttemperature. The mixture was filtered over a pad of kieselgur, which waswashed with dichloromethane. The filtrate was concentrated to yield thedesired product (108 mg, 74%).

LC-MS (method 10): R_(t)=1.98 min; MS (ESIpos): m/z=420 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.76), 0.008(0.69), 0.874 (3.39), 0.892 (7.56), 0.911 (3.45), 1.866 (0.48), 2.208(0.79), 2.293 (0.86), 2.312 (2.31), 2.330 (2.33), 2.349 (0.74), 2.413(14.46), 2.461 (0.57), 2.613 (0.81), 2.928 (15.57), 2.968 (0.53), 3.610(0.56), 3.651 (16.00), 5.755 (1.56), 7.359 (1.87), 7.381 (4.33), 7.403(2.69), 7.428 (1.27), 7.494 (0.44), 7.502 (2.54), 7.507 (1.19), 7.515(2.82), 7.523 (2.36), 7.532 (0.89), 7.537 (1.94), 8.536 (2.69), 9.570(1.37), 10.014 (6.17).

Intermediate 199 ethyl1-[6-({1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethyl)phenyl]-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3-methyl-1H-pyrazole-5-carboxylate

Under an argon atmosphere,1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethyl)phenyl]-1H-pyrazol-5-amine(210 mg, 90% purity, 640 μmol) and sodium phenolate (74.3 mg, 640 μmol)and the contents were suspended in 1,4-dioxane (1.4 mL). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (6.93 mg, 7.56 μmol), XantPhos(10.1 mg, 17.5 μmol) and ethyl1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate (172 mg,90% purity, 582 μmol) were added and the reaction mixture was degassedagain for 1 min. It was then heated at 90° C. overnight while vigorouslystirring. After cooling to ambient temperature, the reaction mixture wasloaded onto silica gel and purified by flash column chromatography (SNAPUltra 25g, cyclohexane/ethyl acetate gradient 95/5 to 20/80) and furtherby preparative HPLC (column: Chromatorex C18; 125*30 mm, 10 μM, flow 75mL/min, gradient acetonitrile/water (containing 0.1% trifluoroaceticacid) 5/95 to 95/5) to yield the desired product (35 mg, 11% yield).

LC-MS (method 9): R_(t)=1.24 min; MS (ESIpos): m/z=526 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.63), −0.023(1.10), 0.147 (0.61), 0.314 (2.53), 0.433 (2.67), 0.453 (2.77), 0.853(0.18), 1.200 (6.38), 1.218 (12.78), 1.236 (8.34), 2.073 (16.00), 2.263(2.55), 2.328 (0.90), 2.367 (0.59), 2.670 (0.88), 2.711 (0.57), 3.875(2.38), 3.892 (2.32), 4.247 (1.94), 4.264 (6.18), 4.282 (6.11), 4.300(1.90), 5.754 (9.42), 6.753 (1.98), 7.793 (3.40), 7.813 (4.65), 7.938(2.77), 7.958 (2.24), 8.431 (0.47), 9.602 (0.35).

Intermediate 200 ethyl4-chloro-1-[6-({1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethyl)phenyl]-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3-methyl-1H-pyrazole-5-carboxylate

Under an argon atmosphere,1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethyl)phenyl]-1H-pyrazol-5-amine(210 mg, 90% purity, 640 μmol) and sodium phenolate (74.3 mg, 640 μmol)and the contents were suspended in 1,4-dioxane (1.4 mL). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (6.93 mg, 7.56 μmol), XantPhos(10.1 mg, 17.5 μmol) and ethyl4-chloro-1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate(234 mg, 75% purity, 582 μmol) were added and the reaction mixture wasdegassed again for 1 min. It was then heated at 90° C. overnight whilevigorously stirring. After cooling to ambient temperature, the reactionmixture was loaded onto silica gel and purified by flash columnchromatography (SNAP Ultra 25g, cyclohexane/ethyl acetate gradient 95/5to 20/80) to yield the desired product (45 mg, 82% purity, 11% yield).

LC-MS (method 10): R_(t)=2.56 min; MS (ESIpos): m/z=560 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.56), 0.146(0.56), 0.310 (2.62), 0.430 (2.76), 0.449 (3.16), 0.851 (0.23), 1.204(1.52), 1.231 (6.14), 1.249 (11.15), 1.267 (5.62), 1.398 (2.20), 1.614(0.26), 1.989 (0.23), 2.034 (1.69), 2.067 (16.00), 2.272 (2.16), 2.327(1.31), 2.367 (0.73), 2.375 (0.45), 2.682 (1.34), 2.710 (0.66), 3.568(0.52), 3.824 (0.49), 3.841 (0.61), 3.872 (2.30), 4.329 (2.11), 4.347(6.30), 4.365 (6.23), 4.383 (2.30), 4.995 (0.47), 7.196 (0.21), 7.724(0.45), 7.793 (3.68), 7.813 (4.87), 7.937 (2.62), 7.956 (1.99), 8.445(0.40), 9.655 (0.33).

Intermediate 201 ethyl 4-(difluoromethyl)benzoate

4-(difluoromethyl)benzoic acid (5.00 g, 29.0 mmol) was suspended inthionyl chloride (15 ml, 210 mmol) and refluxed for 30 minutes. Aftercooling to ambient temperature the mixture was concentrated underreduced pressure. The remaining material was resolved in ethanol (50 ml,860 mmol) and the mixture was refluxed for 1 hour. After cooling toambient temperature, the mixture was concentrated under reducedpressure; the remaining residue was resolved in dichloromethane andwashed with water (2×). The organic phase was dried over sodium sulfateand concentrated under reduced pressure to yield 5.57 g (96%) of thedesired product.

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.014 (1.55), 1.316(7.29), 1.334 (16.00), 1.345 (9.92), 1.352 (9.81), 1.363 (4.50), 3.334(3.11), 4.316 (2.45), 4.333 (7.73), 4.345 (5.91), 4.351 (8.54), 4.362(4.82), 4.369 (3.81), 4.380 (1.50), 6.999 (2.02), 7.009 (1.36), 7.138(3.87), 7.148 (2.59), 7.277 (1.95), 7.287 (1.33), 7.714 (5.37), 7.732(7.17), 8.076 (6.10), 8.094 (6.57), 8.106 (4.09).

Intermediate 2023-[4-(difluoromethyl)phenyl]-2-methyl-3-oxopropanenitrile

A solution of ethyl 4-(difluoromethyl)benzoate (5.20 g, 26.0 mmol) andpropanenitrile (2.8 ml, 39 mmol) in tetrahydrofuran (66 ml, 820 mmol)was treated with a solution of lithium bis(trimethylsilyl)amide (40 ml,1.0 M in tetrahydrofuran, 40 mmol). The mixture was stirred overnight atambient temperature. The mixture was diluted with water and extractedonce with ethyl acetate. The organic phase was discarded. The aqueousphase was acidified with hydrochloric acid and extracted withdichloromethane (2×). The combined organic phases were washed withwater, dried over sodium sulfate and concentrated under reduced pressureto yield 3.52 g (60%) of the desired product.

LC-MS (method 10): R_(t)=1.56 min; MS (ESIneg): m/z=208 [M−H]⁻

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.489 (6.90), 1.506(6.88), 1.679 (2.15), 1.889 (16.00), 1.917 (0.73), 5.152 (0.54), 5.169(1.66), 5.187 (1.64), 5.205 (0.52), 6.961 (1.45), 7.017 (0.99), 7.100(2.84), 7.156 (1.95), 7.240 (1.34), 7.294 (0.95), 7.578 (0.55), 7.665(0.75), 7.688 (14.11), 7.712 (0.95), 7.787 (2.51), 7.807 (2.79), 8.147(3.00), 8.167 (2.67), 10.998 (0.95).

Intermediate 2031-(cyclopropylmethyl)-3-[4-(difluoromethyl)phenyl]-4-methyl-1H-pyrazol-5-amine

A solution of 3-[4-(difluoromethyl)phenyl]-2-methyl-3-oxopropanenitrile(1.75 g, 8.37 mmol) in 2-propanol (18 ml) was treated with(cyclopropylmethyl)hydrazine dihydrochloride (1.73 g, 10.9 mmol). Themixture was stirred overnight at 95° C. After cooling to ambienttemperature and removal of the solvent, the mixture was purified bypreparative HPLC (method: column: Reprosil C18; 10 μm; 125×30 mm/flow:50 mL/min/solvent: A=water (0.01% formic acid), B=acetonitrile/gradient:0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75 min=100% B, 19.75-23.00min=90% B) to yield 1.38 g (60%) of the desired product.

LC-MS (method 10): R_(t)=1.55 min; MS (ESIpos): m/z=278 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.343 (0.56), 0.356(2.14), 0.359 (2.25), 0.368 (2.59), 0.380 (0.97), 0.422 (0.95), 0.431(1.95), 0.442 (1.31), 0.451 (2.19), 0.468 (0.56), 1.198 (0.53), 1.205(0.52), 1.217 (0.83), 1.230 (0.51), 1.235 (0.50), 2.019 (16.00), 3.818(4.07), 3.835 (4.01), 4.986 (0.93), 6.892 (1.14), 7.032 (2.32), 7.172(1.04), 7.555 (2.53), 7.575 (3.22), 7.717 (3.61), 7.738 (2.83).

Intermediate 204 3-(4-chlorophenyl)-2-methyl-3-oxopropanenitrile

A solution of ethyl 4-chlorobenzoate (4.2 ml, 27 mmol) andpropanenitrile (5.8 ml, 81 mmol) in tetrahydrofuran (80 ml, 990 mmol)was treated with a solution of lithium bis(trimethylsilyl)amide (84 ml,1.0 M in tetrahydrofuran, 84 mmol). The mixture was stirred overnight atambient temperature. The mixture was diluted with water and extractedonce with ethyl acetate. The organic phase was discarded. The aqueousphase was acidified with hydrochloric acid and extracted withdichloromethane (2×). The combined organic phases were washed withwater, dried over sodium sulfate and concentrated under reduced pressureto yield 3.52 g (60%) of the desired product.

LC-MS (method 10): R_(t)=1.65 min; MS (ESIpos): m/z=194 [M+H]⁺

Intermediate 2053-(4-chlorophenyl)-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-5-amine

A solution of 3-(4-chlorophenyl)-2-methyl-3-oxopropanenitrile (2.73 g,14 1 mmol) in 2-propanol (51 ml) was treated with(cyclopropylmethyl)hydrazine dihydrochloride (2.92 g, 18.3 mmol). Themixture was refluxed overnight. After cooling to ambient temperature andthe mixture was diluted with water and 1M sodium hydroxide solution wasadded. The mixture was extracted with ethyl acetate (3×). The combinedorganic phases were washed with 1M sodium hydrogen carbonate solution,brine, dried over sodium sulfate and concentrated under reduced pressureto yield 3.62 g (96%) of the desired product.

LC-MS (method 10): R_(t)=1.63 min; MS (ESIpos): m/z=262 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.008 (0.43), 0.331(0.53), 0.344 (2.14), 0.347 (2.30), 0.356 (2.62), 0.369 (0.99), 0.413(0.95), 0.423 (2.01), 0.426 (1.83), 0.433 (1.34), 0.442 (2.28), 0.458(0.58), 1.185 (0.54), 1.191 (0.52), 1.203 (0.83), 1.215 (0.51), 1.223(0.52), 1.988 (16.00), 3.794 (4.27), 3.811 (4.21), 4.934 (4.93), 7.404(3.85), 7.421 (1.50), 7.425 (5.00), 7.591 (4.95), 7.607 (1.40), 7.612(4.05).

Intermediate 2061-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methoxy-1H-pyrazol-5-amine

A solution of 3-(4-fluorophenyl)-2-methoxy-3-oxopropanenitrile (2.50 g,12 9 mmol) in 2-propanol (50 mL) was treated with(cyclopropylmethyl)hydrazine dihydrochloride (2.68 g, 16.8 mmol). Themixture was refluxed overnight. After cooling to ambient temperature themixture concentrated under reduced pressure. The remaining residue wastaken up in acetonitrile, crystalline material was collected byfiltration. The solid material was resolved in ethyl acetate and washedwith 1M sodium hydroxide solution. The organic phase was dried oversodium sulfate and concentrated under reduced pressure to yield 1.58 gof the desired product (47%).

LC-MS (method 10): R_(t)=1.57 min; MS (ESIpos): m/z=262 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.91), 0.008(0.78), 0.337 (2.14), 0.349 (7.29), 0.353 (7.32), 0.362 (8.28), 0.365(7.78), 0.374 (3.16), 0.391 (0.76), 0.398 (0.75), 0.411 (1.24), 0.427(3.40), 0.436 (6.54), 0.440 (5.92), 0.447 (4.35), 0.456 (7.12), 0.460(5.63), 0.472 (1.88), 1.171 (0.70), 1.176 (0.97), 1.189 (1.75), 1.191(1.72), 1.196 (1.75), 1.208 (2.72), 1.216 (1.43), 1.220 (1.64), 1.226(1.57), 1.228 (1.56), 1.240 (0.77), 1.245 (0.57), 3.317 (16.00), 3.762(13.65), 3.780 (13.34), 4.989 (15.04), 7.164 (1.07), 7.171 (6.91), 7.176(2.91), 7.188 (3.41), 7.193 (14.02), 7.211 (2.63), 7.216 (7.35), 7.223(1.01), 7.792 (1.22), 7.799 (7.39), 7.805 (3.57), 7.814 (8.23), 7.822(8.20), 7.831 (3.02), 7.836 (6.97), 7.843 (0.92).

Intermediate 2074-[5-amino-1-(cyclopropylmethyl)-4-methoxy-1H-pyrazol-3-yl]benzonitrile

A solution of 4-[cyano(methoxy)acetyl]benzonitrile (1.81 g, 9.04 mmol)and (cyclopropylmethyl)hydrazine dihydrochloride (1.87 g, 11.8 mmol) in2-propanol (36 ml) wsa refluxed overnight. After cooling to ambienttemperature the crude product was purified by flash-chromatography onsilica gel (column: Biotage DNAP Ultra 25 g, solvent: 12%dichloromethane/88% ethyl acetate to 100% ethyl acetate) to yield 1.58 g(63%) of the desired product.

LC-MS (method 10): R_(t)=1.53 min; MS (ESIpos): m/z=269 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.350 (1.94), 0.363(8.44), 0.365 (8.46), 0.375 (9.90), 0.387 (3.18), 0.406 (0.76), 0.410(0.74), 0.424 (1.04), 0.441 (3.14), 0.451 (7.31), 0.471 (8.02), 0.486(1.91), 1.176 (0.51), 1.195 (1.18), 1.207 (1.98), 1.214 (1.94), 1.226(2.94), 1.238 (1.91), 1.244 (1.91), 1.257 (0.93), 1.321 (0.67), 1.336(0.67), 3.173 (0.42), 3.323 (3.32), 3.481 (0.66), 3.611 (0.53), 3.804(14.03), 3.821 (14.13), 4.158 (0.71), 5.120 (13.03), 7.807 (11.20),7.828 (14.44), 7.944 (0.86), 7.964 (16.00), 7.985 (12.23), 8.012 (0.50).

Intermediate 208 3-(4-chlorophenyl)-1,4-dimethyl-1H-pyrazol-5-amine

A solution of 3-(4-chlorophenyl)-2-methyl-3-oxopropanenitrile (2.67 g,13.8 mmol) and methylhydrazine (730 μl, 14 mmol) in toluene was treatedwith acetic acid (790 μl, 14 mmol) and stirred for 2 days at ambienttemperature and 2 additional days at 80° C. The mixture was diluted withwater and the volume was reduced under reduced pressure. The mixture wasextracted with ethyl acetate (3×). The combined organic phases werewashed with water, brine, dried over sodium sulfate and concentratedunder reduced pressure. The crude product was purified using preparativeHPLC (column: XBridge C18, 5 μM, 75×30 mm, flow 80 mL/min, solvents: A(water), B (acetonitrile/water 80/20 +2% formic acid), C (acetonitrile),gradient: 0.00-1.00 min 85% A/10% B/5% C, 1.00-7.20 min to 60% A/10%B/30% C, 7.20-7.40 min to 5% A/10% B/85% C, keep until 8.30 min,8.30-8.80 min 85% A/10% B/5% C keep until 10.60 min) to yield 1.20 g ofthe desired product (37%) along with its regioisomer (250 mg, 9.6%).

LC-MS (method 9): R_(t)=0.71 min; MS (ESIpos): m/z=222 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.987 (16.00), 2.013(0.56), 3.650 (0.44), 4.987 (3.15), 7.396 (0.66), 7.401 (3.95), 7.405(1.44), 7.415 (1.69), 7.419 (4.67), 7.424 (0.79), 7.577 (0.85), 7.582(4.91), 7.586 (1.62), 7.596 (1.56), 7.599 (3.89), 7.604 (0.64).

Intermediate 209 5-(4-chlorophenyl)-1,4-dimethyl-1H-pyrazol-3-amine

A solution of 3-(4-chlorophenyl)-2-methyl-3-oxopropanenitrile (2.67 g,13.8 mmol) and methylhydrazine (730 μl, 14 mmol) in toluene was treatedwith acetic acid (790 μl, 14 mmol) and stirred for 2 days at ambienttemperature and 2 additional days at 80° C. The mixture was diluted withwater and the volume was reduced under reduced pressure. The mixture wasextracted with ethyl acetate (3×). The combined organic phases werewashed with water, brine, dried over sodium sulfate and concentratedunder reduced pressure. The crude product was purified using preparativeHPLC (column: XBridge C18, 5 μM, 75×30 mm, flow 80 mL/min, solvents: A(water), B (acetonitrile/water 80/20+2% formic acid), C (acetonitrile),gradient: 0.00-1.00 min 85% A/10% B/5% C, 1.00-7.20 min to 60% A/10%B/30% C, 7.20-7.40 min to 5% A/10% B/85% C, keep until 8.30 min,8.30-8.80 min 85% A/10% B/5% C keep until 10.60 min) to yield 250 mg ofthe desired product (9.6%) along with its regioisomer (1.2 g, 37%).

LC-MS (method 9): R_(t)=0.75 min; MS (ESIpos): m/z=222 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.381 (0.41), 1.765(16.00), 1.799 (1.38), 1.984 (2.99), 2.074 (0.69), 3.195 (1.30), 3.314(10.21), 3.561 (3.09), 4.479 (0.94), 4.977 (1.02), 7.053 (0.47), 7.276(0.43), 7.362 (3.45), 7.382 (4.55), 7.397 (0.76), 7.418 (0.81), 7.454(0.41), 7.534 (4.14), 7.555 (3.40), 7.577 (1.00), 7.599 (0.85).

Intermediate 2102-[1-(2-cyclopropyl-2-oxoethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione

2-[5-(4-fluorophenyl)-4-methyl-1H-pyrazol-3-yl]-1H-isoindole-1,3(2H)-dione(5.80 g, 18.0 mmol) and potassium carbonate (4.99 g, 36.1 mmol) weresuspended in dimethylformamide (25 mL) and 2-bromo-1-cyclopropylethanone(5.00 g, 30.7 mmol) was slowly added under an argon atmosphere. Thereaction mixture was stirred at ambient temperature overnight. Water wasadded and the mixture stirred for another 5 min. The precipitated solidwas collected by filtration and washed with water. It was then dried ina vacuum drying-oven at 40° C. overnight. Further purification by flashcolumn chromatography (SNAP Ultra 100g, cyclohexane/ethyl acetategradient 88/12 to 10/90) yielded the desired product (3.78 g, 49%yield).

LC-MS (method 10): R_(t)=2.03 min; MS (ESIpos): m/z=404 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.98), 0.008(1.97), 0.767 (0.68), 0.778 (1.87), 0.785 (2.92), 0.797 (2.56), 0.804(1.55), 0.825 (0.66), 0.838 (1.45), 0.844 (2.53), 0.852 (1.60), 0.857(1.74), 0.864 (2.97), 0.872 (1.54), 0.883 (0.70), 1.157 (1.19), 1.175(2.38), 1.192 (1.21), 1.891 (0.74), 1.898 (0.81), 1.910 (1.37), 1.921(0.80), 1.929 (0.68), 1.980 (0.68), 1.988 (4.43), 2.008 (0.44), 2.037(16.00), 4.020 (1.04), 4.038 (1.05), 5.180 (8.30), 7.277 (2.31), 7.300(4.83), 7.317 (0.97), 7.322 (2.58), 7.721 (2.60), 7.726 (1.28), 7.735(2.87), 7.743 (2.72), 7.751 (1.07), 7.757 (2.31), 7.949 (2.74), 7.957(2.87), 7.963 (2.78), 7.971 (4.37), 7.981 (0.77), 8.010 (0.72), 8.020(4.33), 8.027 (2.71), 8.034 (2.87), 8.041 (2.45).

Intermediate 2112-{1-[(±)-2-cyclopropyl-2-hydroxypropyl]-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl}-1H-isoindole-1,3(2H)-dione(racemate)

Under an argon atmosphere,2-[1-(2-cyclopropyl-2-oxoethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(500 mg, 1.24 mmol) was dissolved in tetrahydrofuran (8 mL) and cooledto 0° C. A solution of methylmagnesium bromide in tetrahydrofuran (1.9mL, 1.0 M, 1.9 mmol). After 2 h, a second aliquot methylmagnesiumbromide in tetrahydrofuran (1.5 mL, 1.0 M, 1.5 mmol) was added and thereaction mixture was stirred overnight at ambient temperature. A thirdaliquot methylmagnesium bromide in tetrahydrofuran (1.5 mL, 1.0 M, 1.5mmol) was added and the reaction mixture was stirred at ambienttemperature for 2 h. It was then carefully quenched by addition ofNa₂EDTA solution (10%) and extracted with ethyl acetate (2×). Thecombined organic phase extracts were dried over sodium sulfate,concentrated and to yield a complex mixture that was used in the nextstep without further purification.

LC-MS (method 11): Rt=1.38 min; MS (ESIpos): m/z=420 [M+H]⁺

Intermediate 212(±)-1-[5-amino-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-1-yl]-2-cyclopropylpropan-2-ol(racemate)

The complex mixture containing2-{1-[(2S)-2-cyclopropyl-2-hydroxypropyl]-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl}-1H-isoindole-1,3(2H)-dione(510 mg, 1.22 mmol) was dissolved in ethanol (18 mL) and hydrazinemonohydrate (300 μL, 6.1 mmol) and acetic acid (210 μL, 3.6 mmol) wereadded. The reaction mixture was stirred under reflux for 3 h and allowedto cool to ambient temperature and left standing overnight. Water wasadded to the mixture, which was then extracted with ethyl acetate. Theorganic phase extract was washed with aqueous saturated sodiumhydrogencarbonate solution, dried over sodium sulfate and concentrated.The residue was purified by flash column chromatography (SNAP Ultra 25g, cyclohexane/ethyl acetate gradient 90/10 to 0/100) to yield thedesired product (39 mg, 11% yield).

LC-MS (method 11): R_(t)=1.03 min; MS (ESIpos): m/z=290 [M+H]⁺, 272[M-water+H]⁺

Intermediate 213 2-methyl-3-oxo-3-(pyridin-4-yl)propanenitrile

Ethyl pyridine-4-carboxylate (5.0 ml, 33 mmol) and propanenitrile (5.9ml, 83 mmol) were dissolved in tetrahydrofuran (47 mL) and chilled witha waterbath. A solution of lithium bis(trimethylsilyl)amide (84 mL, 1.0M, 84 mmol) was slowly added and vigorous stirring. A pale yellow solidstarts precipitating immediately. After 30 min, the precipitated solidwas collected by filtration, washed with with tetrahydrofuran and driedunder vacuum. It was then suspended in ethyl acetate and aqueousammonium chloride solution and adjusted to pH 4-5 with aqueoushydrochloric acid solution (1 M). After phase separation, the aqueouslayer was extracted with ethyl acetate (2×). The combined organic phaseextracts were dried over sodium sulfate and concentrated to yield thedesired product (4.08 g, 75% yield).

LC-MS (method 11): R_(t)=0.53 min; MS (ESIpos): m/z=161 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.18), −0.008(1.47), 0.008 (1.67), 0.146 (0.17), 1.085 (0.38), 1.104 (0.19), 1.471(0.66), 1.484 (0.67), 1.564 (0.55), 1.676 (3.26), 1.884 (16.00), 2.328(0.20), 2.367 (0.17), 2.523 (0.54), 2.670 (0.22), 2.711 (0.18), 5.143(0.19), 7.412 (0.74), 7.416 (0.55), 7.427 (0.81), 7.523 (4.17), 7.538(4.45), 7.874 (0.49), 8.694 (4.40), 8.708 (4.64), 8.873 (0.44), 11.166(0.44).

Intermediate 2141-(cyclopropylmethyl)-4-methyl-3-(pyridin-4-yl)-1H-pyrazol-5-amine

2-methyl-3-oxo-3-(pyridin-4-yl)propanenitrile (2.00 g, 12.5 mmol) and(cyclopropylmethyl)hydrazine dihydrochloride (2.48 g, 15.6 mmol) weresuspended in 2-propanol (28 ml) and the reaction mixture heated toreflux for 4.5 h while vigorously stirring. After cooling to ambienttemperature, the reaction mixture was carefully quenched by addition ofsaturated aqueous sodium hydrogencarbonate solution and extracted withethyl acetate (3×). The combined organic phase extracts were dried oversodium sulfate and concentrated to yield the desired product (2.04 g,69% yield).

LC-MS (method 9): R_(t)=0.64 min; MS (ESIpos): m/z=229 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.343 (0.53), 0.358(2.52), 0.370 (2.88), 0.380 (1.02), 0.424 (0.95), 0.436 (2.10), 0.443(1.47), 0.453 (2.33), 0.468 (0.56), 1.200 (0.61), 1.205 (0.56), 1.218(0.89), 1.230 (0.56), 1.237 (0.59), 2.053 (16.00), 3.830 (4.48), 3.847(4.45), 5.025 (5.06), 7.567 (4.07), 7.571 (3.53), 7.579 (2.63), 7.583(4.73), 8.516 (3.90), 8.519 (3.54), 8.527 (2.45), 8.531 (4.43).

Intermediate 2151-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylicacid

A solution of ethyl1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(1.38 g, 2.81 mmol) in tetrahydrofuran (19 ml, 230 mmol) was treatedwith aqueous lithium hydroxide solution (14 ml, 1.0 M, 14 mmol) andstirred for 2 days at ambient temperature followed by reflux overnight.After cooling to room temperature the mixture was diluted with water andacidified with hydrochloric acid. The mixture was extracted with ethylacetate (3×). The combined organic phases were dried over sodium sulfateand concentrated under reduced pressure to yield 977 mg (75%) of thedesired product.

LC-MS (method 10): R_(t)=1.86 min; MS (ESIpos): m/z=462 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.304 (2.49), 0.313(2.57), 0.435 (2.69), 0.450 (2.75), 1.183 (0.42), 1.193 (0.77), 1.199(0.76), 1.209 (1.18), 1.215 (0.62), 1.218 (0.69), 1.223 (0.71), 1.917(2.17), 2.018 (16.00), 2.367 (1.57), 2.914 (12.32), 3.573 (2.49), 3.842(1.91), 3.855 (1.85), 7.258 (2.57), 7.262 (1.13), 7.276 (5.09), 7.294(2.73), 7.722 (1.48), 7.733 (1.99), 7.749 (1.37), 12.614 (0.58).

Intermediate 216N′-acetyl-1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbohydrazide

A solution of1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylicacid (500 mg, 1.08 mmol) and acetohydrazide (241 mg, 3.25 mmol) inN,N-dimethylformamide (8.3 mL) was treated with HATU (618 mg, 1.63 mmol)and N,N-diisopropylethylamine (570 3.3 mmol) and stirred one hour atroom temperature. The mixture was diluted with water. The occurringprecipitate was collected by filtration, washed with water and dried toyield 415 mg (72%) of the desired product.

LC-MS (method 9): R_(t)=0.83 min; MS (ESIpos): m/z=518 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.006 (0.64), 0.300(3.00), 0.308 (3.08), 0.430 (3.14), 0.446 (3.20), 1.078 (1.98), 1.092(3.92), 1.106 (1.99), 1.178 (0.58), 1.188 (1.00), 1.193 (1.00), 1.203(1.42), 1.212 (0.95), 1.217 (0.96), 1.227 (0.56), 1.882 (1.07), 1.907(13.23), 2.015 (16.00), 2.293 (1.94), 2.691 (2.06), 2.733 (1.43), 2.774(13.51), 2.891 (1.58), 3.363 (0.68), 3.376 (1.92), 3.390 (1.89), 3.404(0.63), 3.838 (2.46), 3.850 (2.40), 7.258 (2.54), 7.276 (4.99), 7.293(2.74), 7.734 (2.38), 8.519 (0.48), 9.726 (2.68), 9.893 (3.50).

Intermediate 2171-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbaldehyde

4,6-dichloropyrimidine (6.30 g, 42.3 mmol),3,5-dimethyl-1H-pyrazole-4-carbaldehyde (5.00 g, 40.3 mmol) and cesiumcarbonate (13.1 g, 40.3 mmol) were suspended in dimethylformamide andthe reaction mixture was stirred overnight at ambient temperature. Itwas then poured onto water (400 mL) and stirred for another 30 min. Theprecipitated solid was collected by filtration, washed with water anddried overnight in a dessicator to yield the desired product, which wasused in the next step without further purification (7.1 g, 68% purity,48% yield).

LC-MS (method 11): R_(t)=1.19 min; MS (ESIpos): m/z=236 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.008 (0.44), 2.284(0.49), 2.403 (0.64), 2.421 (0.45), 2.432 (0.60), 2.450 (16.00), 2.478(2.29), 2.732 (0.75), 2.771 (0.56), 2.891 (0.89), 2.947 (0.58), 2.976(15.72), 3.024 (1.91), 8.020 (2.96), 8.022 (2.99), 9.032 (2.87), 9.035(2.85), 10.054 (6.02), 10.069 (0.82).

Intermediate 218 4-[1-(cyclopropylmethyl)-5-{[6-(4-formyl-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-4-methyl-1H-pyrazol-3-yl]benzonitrile

A microwave vial was charged with4-[5-amino-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(96.9 mg, 384 μmol),1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbaldehyde (100mg, 423 μmol) and sodium phenolate (49.1 mg, 423 μmol) and the contentswere suspended in 1,4-dioxane (1.4 mL). The reaction mixture wasdegassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (7.04mg, 7.68 μmol) and XantPhos (8.89 mg, 15.4 μmol) were added and thereaction mixture was degassed again for 1 min. The vial was sealed andheated at 85° C. overnight while vigorously shaking. After cooling toambient temperature, the reaction mixture was diluted with water andextracted with ethyl acetate. The organic phase extract was dried oversodium sulfate and concentrated. The residue was purified by flashcolumn chromatography (SNAP Ultra 25g, cyclohexane/ethyl acetategradient 90/10 to 0/100) and further by preparative HPLC (column:Chromatorex C18; 250*30 mm, 10 μM, flow 100 mL/min, gradientacetonitrile/water (containing 0.1% trifluoroacetic acid) 10/90 to90/10) to yield the desired product (24 mg, 14% yield).

LC-MS (method 11): R_(t)=1.36 min; MS (ESIpos): m/z=453 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (3.29), 0.008(2.64), 0.308 (2.58), 0.320 (2.81), 0.436 (2.67), 0.456 (2.80), 1.192(0.71), 1.211 (1.07), 1.230 (0.75), 2.030 (0.43), 2.065 (16.00), 2.328(0.93), 2.367 (0.73), 2.407 (2.23), 2.670 (0.84), 2.943 (14.84), 3.866(3.62), 3.884 (3.85), 3.940 (2.51), 7.885 (1.10), 7.908 (13.70), 8.546(0.51), 9.599 (0.42), 10.016 (3.38).

Intermediate 2191,4-dimethyl-3-[4-(trifluoromethyl)phenyl]-1H-pyrazol-5-amine

Under an argon atmosphere,2-methyl-3-oxo-3-[4-(trifluoromethyl)phenyl]propanenitrile (1.00 g, 4.40mmol) was dissolved in 1,4-dioxane (24 mL) and methylhydrazine (230 μl,4.4 mmol) and acetic acid (250 μl, 4.4 mmol) were added. The reactionmixture was stirred at ambient temperature. It was then concentrated andthe residue redissolved in ethanol (12 mL) and purified by preparativeHPLC (Daicel Chiralpak IF 5 μm, 250×20 mm, flow: 15 mL/min, isocraticn-Heptane/ethanol 75/25, 350 μL injections every 15 min) to yield thedesired product (469 mg, 38% yield) along with1,4-dimethyl-5-[4-(trifluoromethyl)phenyl]-1H-pyrazol-3-amine (seebelow).

LC-MS (method 9): R_(t)=0.83 min; MS (ESIpos): m/z=256 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.157 (0.45), 1.909(1.35), 2.033 (16.00), 3.313 (2.26), 5.037 (3.43), 7.698 (2.25), 7.718(3.47), 7.795 (3.33), 7.816 (2.19).

Intermediate 2201,4-dimethyl-5-[4-(trifluoromethyl)phenyl]-1H-pyrazol-3-amine

The title compound was observed as a by-product during the synthesis of1,4-dimethyl-3-[4-(trifluoromethyl)phenyl]-1H-pyrazol-5-amine (seeabove). It was obtained after purification by preparative HPLC (DaicelChiralpak IF 5 μm, 250×20 mm, flow: 15 mL/min, isocraticn-Heptane/ethanol 75/25, 350 μL injections every 15 min) as a whitesolid (120 mg, 11% yield).

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.39), 1.798(16.00), 1.908 (0.59), 3.313 (7.17), 3.678 (0.17), 4.526 (2.20), 7.582(2.82), 7.603 (3.27), 7.833 (3.37), 7.854 (2.90).

Intermediate 221 3-(2,4-difluorophenyl)-1,4-dimethyl-1H-pyrazol-5-amine

Under an argon atmosphere,3-(2,4-difluorophenyl)-2-methyl-3-oxopropanenitrile (2.00 g, 10.2 mmol)was dissolved in 1,4-dioxane (57 mL) and methylhydrazine (550 μl, 10mmol) and acetic acid (590 μl, 10 mmol) were added. The reaction mixturewas stirred at ambient temperature. It was then concentrated and theresidue redissolved in ethanol (12 mL) and purified by preparative HPLC(Daicel Chiralpak IF 5 μm, 250×20 mm, flow: 15 mL/min, isocraticn-Heptane/ethanol 75/25, 300 μL injections every 15 min) to yield thedesired product (1.93 g, 71% yield) along with5-(2,4-difluorophenyl)-1,4-dimethyl-1H-pyrazol-3-amine (see below).

LC-MS (method 9): R_(t)=0.66 min; MS (ESIpos): m/z=224 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.762 (15.97), 1.767(16.00), 1.911 (4.69), 2.075 (1.15), 2.503 (6.48), 2.884 (0.46), 3.322(3.24), 4.979 (6.91), 7.067 (1.05), 7.073 (1.10), 7.089 (2.21), 7.094(2.28), 7.110 (1.22), 7.116 (1.24), 7.226 (1.18), 7.233 (1.07), 7.252(1.99), 7.277 (1.18), 7.282 (1.07), 7.404 (1.33), 7.425 (2.62), 7.443(2.61), 7.464 (1.17).

Intermediate 222 5-(2,4-difluorophenyl)-1,4-dimethyl-1H-pyrazol-3-amine

The title compound was observed as a by-product during the synthesis of3-(2,4-difluorophenyl)-1,4-dimethyl-1H-pyrazol-5-amine (see above). Itwas obtained after purification by preparative HPLC (Daicel Chiralpak IF5 μm, 250×20 mm, flow: 15 mL/min, isocratic n-Heptane/ethanol 75/25, 300μL injections every 15 min) as a white solid (249 mg, 11% yield).

LC-MS (method 9): Rt=0.70 min; MS (ESIpos): m/z=224 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.16), 1.690(16.00), 1.908 (0.65), 2.327 (0.24), 2.670 (0.29), 3.377 (14.94), 3.397(0.28), 3.556 (0.26), 3.563 (0.24), 4.479 (3.40), 7.198 (0.60), 7.204(0.65), 7.219 (1.32), 7.225 (1.41), 7.240 (0.76), 7.246 (0.80), 7.391(0.74), 7.397 (0.74), 7.407 (0.91), 7.416 (1.33), 7.423 (2.05), 7.428(1.76), 7.445 (2.13), 7.466 (0.73).

Intermediate 2231-(cyclopropylmethyl)-3-(2,4-difluorophenyl)-4-methyl-1H-pyrazol-5-amine

3-(2,4-difluorophenyl)-2-methyl-3-oxopropanenitrile (2.19 g, 11.2 mmol)and (cyclopropylmethyl)hydrazine dihydrochloride (2.24 g, 100% purity,14.1 mmol) were suspended in 2-propanol (23 mL) and the reaction mixturewas stirred under reflux for 3 h. It was then concentrated to ⅓ of itsoriginal volume, carefully quenched with aqueous saturated sodiumhydrogencarbonate solution and extracted with ethyl acetate (3×). Thecombined organic phase extracts were washed with brine, dried oversodium sulfate and concentrated. The residue was dissolved indichloromethane, loaded onto silica gel and purified by flash columnchromatography (SNAP Ultra 25 g, cyclohexane/ethyl acetate gradient100/0 to 40/60) to yield the desired product (1.58 g, 52% yield).

LC-MS (method 9): R_(t)=0.77 min; MS (ESIpos): m/z=264 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.328 (0.97), 0.341(3.95), 0.344 (3.91), 0.353 (4.63), 0.366 (1.76), 0.402 (0.58), 0.418(1.74), 0.427 (3.64), 0.431 (3.15), 0.438 (2.26), 0.448 (4.03), 0.451(3.13), 0.463 (1.09), 1.170 (0.47), 1.175 (0.46), 1.182 (0.92), 1.190(0.90), 1.194 (0.78), 1.202 (1.46), 1.210 (0.73), 1.214 (0.87), 1.219(0.85), 1.222 (0.83), 1.234 (0.43), 1.770 (16.00), 1.776 (15.36), 3.651(0.60), 3.793 (7.85), 3.810 (7.77), 3.934 (0.45), 4.935 (7.16), 4.996(0.54), 7.072 (1.00), 7.078 (1.07), 7.094 (2.12), 7.100 (2.23), 7.115(1.17), 7.121 (1.22), 7.228 (1.27), 7.235 (1.20), 7.252 (1.78), 7.255(1.85), 7.258 (1.80), 7.278 (1.30), 7.285 (1.20), 7.420 (1.31), 7.437(1.70), 7.441 (2.67), 7.458 (2.61), 7.463 (1.51), 7.480 (1.17).

Intermediate 2242-{1-[(±)-2-cyclopropyl-2-hydroxyethyl]-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl}-1H-isoindole-1,3(2H)-dione(racemate)

Under an argon atmosphere,2-[1-(2-cyclopropyl-2-oxoethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(500 mg, 1.24 mmol) was dissolved in toluene (8.0 mL) and cooled to −78°C. A solution of DIBAl-H in toluene (1.1 ml, 1.2 M, 1.4 mmol) was thenadded dropwise. After complete addition, the −reaction mixture wasallowed to warm to 0° C. and stirred for further 1.75 h. A secondaliquot of DIBAl-H (800 μL, 1.2 m, 0.96 mmol) was added and the reactionmixture further stirred for 1.5 h. It was then quenched by addition ofaqueous Rochelle salt solution (20%) and stirred at ambient temperatureovernight. The mixture was extracted with ethyl acetate (2×). Thecombined organic phase extracts were dried over sodium sulfate andconcentrated to yield the desired product that was used in the next stepwithout further purification.

LC-MS (method 11): R_(t)=1.37 min; MS (ESIneg): m/z=404 [M−H]⁻

Intermediate 225(±)-2-[5-amino-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-1-yl]-1-cyclopropylethanol(racemate)

2-{1-[(2S)-2-cyclopropyl-2-hydroxyethyl]-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl}-1H-isoindole-1,3(2H)-dione(456 mg, 1.12 mmol) was dissolved in ethanol (16 mL) and hydrazinemonohydrate (270 μL, 5.6 mmol) and acetic acid (320 μL, 5.6 mmol) wereadded subsequently. The reaction mixture was heated to reflux for 4 h.After cooling to ambient temperature, it was diluted with water andextracted with ethyl acetate. The organic phase extract was washed withaqueous saturated sodium hydrogencarbonate solution, dried over sodiumsulfate and concentrated. The residue was purified by flash columnchromatography (SNAP Ultra 25 g, cyclohexane/ethyl acetate 80/20 to0/100) to yield the desired product (186 mg, 77% purity, 46% yield) andwas used as such in the next step.

LC-MS (method 11): R_(t)=0.94 min; MS (ESIpos): m/z=276 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.83), 0.008(0.59), 0.124 (0.43), 0.134 (0.64), 0.146 (1.10), 0.151 (0.85), 0.159(0.82), 0.163 (0.77), 0.252 (0.65), 0.258 (0.76), 0.265 (0.75), 0.271(0.89), 0.284 (0.64), 0.293 (0.53), 0.351 (2.20), 0.356 (1.70), 0.371(2.19), 0.377 (1.70), 0.825 (0.41), 0.832 (0.48), 0.845 (0.86), 0.852(0.56), 0.857 (0.55), 0.864 (0.80), 0.876 (0.41), 1.983 (16.00), 3.266(0.60), 3.274 (0.72), 3.285 (1.16), 3.296 (0.98), 3.885 (0.78), 3.904(0.70), 3.920 (1.66), 3.939 (1.61), 3.971 (1.61), 3.981 (1.60), 4.006(0.75), 4.016 (0.67), 4.859 (4.87), 5.019 (2.65), 5.031 (2.61), 7.164(1.98), 7.186 (4.23), 7.203 (0.78), 7.208 (2.36), 7.569 (2.25), 7.575(0.98), 7.584 (2.52), 7.591 (2.50), 7.600 (0.93), 7.606 (2.16), 7.930(0.51), 8.366 (0.45).

Intermediate 2264-chloro-6-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidine

4,6-dichloropyrimidine (4.54 g, 30.5 mmol),3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazole (5.00 g, 30.5 mmol) andcesium carbonate (9.93 g, 30.5 mmol) were suspended in dimethylformamide(18 mL) and stirred at ambient temperature overnight. The crude mixturewas poured onto water (400 mL) and further stirred for 30 min. Theprecipitated solid was collected by filtration and washed with water. Itwas then dried in a vacuum drying-oven at 40° C. overnight to yield thedesired product (6.10 g, 69% yield).

LC-MS (method 10): R_(f)=2.33 min; MS (ESIpos): m/z=277 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (0.88), 0.006(0.45), 1.231 (0.20), 1.996 (0.18), 2.003 (0.19), 2.080 (0.19), 2.096(0.19), 2.192 (1.29), 2.216 (0.38), 2.283 (1.29), 2.348 (16.00), 2.350(15.23), 2.364 (0.57), 2.374 (1.89), 2.376 (1.79), 2.521 (0.42), 2.525(0.32), 2.638 (0.19), 2.733 (0.33), 2.793 (15.68), 2.796 (14.90), 2.842(1.73), 2.844 (1.66), 2.892 (0.36), 8.004 (7.87), 8.006 (7.48), 8.260(0.44), 9.028 (7.17), 9.029 (6.81), 9.100 (0.44).

Intermediate 2271-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbaldehyde

Under an argon atmosphere,1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine(1.50 g, 6.11 mmol),1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbaldehyde (1.59g, 6.73 mmol) and sodium phenolate (781 mg, 6.73 mmol) were suspended in1,4-dioxane (25 mL). The reaction mixture was degassed with Ar for 3min. Tris(dibenzylideneacetone)dipalladium (168 mg, 183 μmol) andXantPhos (212 mg, 367 μmol) were added and the reaction mixture wasdegassed again for 1 min and heated at 90° C. for 2 h while vigorouslystirring. After cooling to ambient temperature, the reaction mixture wasloaded onto Celite and purified by flash column chromatography (SNAPUltra 25g, cyclohexane/ethyl acetate gradient 90/10 to 0/100) to yieldan impure product. This was dissolved in acetonitrile at 60° C. and thesolution allowed to cool to ambient temperature overnight. Theprecipitated sold was collected by filtration and later combined withthe other product fraction. The filtrate was concentrated and purifiedby preparative HPLC (method 3) to yield the product. After combiningboth product fraction, the desired product was obtained (286 mg, 10%yield).

LC-MS (method 11): R_(t)=1.41 min; MS (ESIpos): m/z=446 [M+H]⁺

Intermediate 228 2,4-dioxopentan-3-yl acetate

In a 100 ml round-bottom flask was added dimethylsulfoxide and it wasdegassed with Ar. 3-chloropentane-2,4-dione (8.4 ml, 74 mmol) and sodiumacetate (6.10 g, 74 3 mmol) were added under argon and the resultingsolution stirred at ambient temperature. After 3 h, the mixture wasdiluted with water (500 mL) & washed with saturated ammonium chloride(Caution:exothermic!), then extracted with dichloromethane (3×40 ml).The combined organic phase extracts were combined, washed with brine,dried over sodium sulfate and concentrated. The resulting liquid wasdried further overnight under high vacuum to remove residualdimethylsulfoxide to yield the desired product as a colorless liquid(12.7 g, 90% purity, 97% yield).

GC-MS (method 15): R_(t)=2.47 min; MS (EI): m/z=158 (5), 116(77), 101(18), 74 (100).

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.006 (0.83), 2.187(8.60), 2.222 (16.00), 5.655 (2.46).

Intermediate 229 1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-ylacetate

Under an argon atmosphere, 2,4-dioxopentan-3-yl acetate (7.1 ml, 88%purity, 70 mmol) and 4-chloro-6-hydrazinylpyrimidine (11.2 g, 77.5 mmol)were dissolved in ethanol (100 mL). The reaction mixture was refluxedfor 3 h. After cooling to ambient temperature, water was added and thereaction mixture quenched with solid sodium hydrogencarbonate. It wasextracted with dichloromethane (3×). The combined organic phase extractswere washed with brine, dried over magnesium sulfate and concentrated.The residue was purified by flash column chromatography (SNAP Ultra 100g, cyclohexane/ethyl acetate 100/0 to 0/100) and further repurified byflash column chromatography (SNAP Ultra 100 g, cyclohexane/ethyl acetate100/0 to 60/40) to yield the desired product (7.59 g, 40% yield) alongwith the saponified by-product1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-ol (4.48 g, 28%yield, see below).

LC-MS (method 11): R_(t)=1.28 min; MS (ESIpos): m/z=267 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.123 (14.63), 2.344(16.00), 2.517 (14.59), 7.899 (3.66), 7.901 (3.58), 8.903 (3.35), 8.905(3.23).

Intermediate 230 1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-ol

This compound was obtained as a by-product during the synthesis of1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl acetate afterflash column chromatography (SNAP Ultra 100 g, cyclohexane/ethyl acetate100/0 to 60/40) to yield the title compound (4.48 g, 28% yield). It canalso be prepared by the following procedure:

1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl acetate (130 mg,487 μmol) was dissolved in methanol (10 mL) and potassium carbonate (135mg, 075 μmol) was added at 0° C. The reaction mixture was stirred for 5min before being quenched by addition of saturated ammonium chloridesolution and water. It was extracted with ethyl acetate (3×) and thecombined organic phase extracts were dried over sodium sulfate andconcentrated. The desired product thus obtained (94 mg, 86% yield) wasused in the next step without further purification.

LC-MS (method 11): R_(t)=1.26 min; MS (ESIpos): m/z=267 [M+H]⁺

Intermediate 2314-chloro-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine

Under an argon atmosphere,1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-ol (1.50 g, 6.68mmol) was dissolved in dimethylformamide and treated with methyl iodide(0.50 mL, 8.0 mmol) and cesium carbonate (2.61 g, 8.01 mmol). Theresulting suspension was allowed to stir overnight at ambienttemperature. Water was added and the precipitated solid extracted withethyl acetate. The organic phase extract was dried over sodium sulfateand concentrated. The residue was purified by flash columnchromatography (SNAP Ultra 100g, cyclohexane/ethyl acetate gradient) toyield the desired product (1.03 g, 64% yield).

LC-MS (method 9): Rt=1.01 min; MS (ESIpos): m/z=239 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.211 (0.56), 2.239(12.18), 2.579 (12.12), 3.713 (0.75), 3.736 (16.00), 7.854 (2.75), 7.856(2.71), 8.870 (2.40), 8.871 (2.36).

Intermediate 232 ethyl1-(6-{[1-(cyclopropylmethyl)-4-methyl-3-(pyridin-4-yl)-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

A microwave vial was charged with ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (318mg, 95% purity, 1.08 mmol),1-(cyclopropylmethyl)-4-methyl-3-(pyridin-4-yl)-1H-pyrazol-5-amine (300mg, 90% purity, 1.18 mmol) and sodium phenolate (137 mg, 1.18 mmol) andthe contents were suspended in 1,4-dioxane (3.4 mL). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (19.7 mg, 21.5 μmol) and XantPhos(24.9 mg, 43.0 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously shaking. After cooling to ambient temperature, thereaction mixture was filtered and concentrated. The residue wasredissolved in dimethylsulfoxide and purified by preparative HPLC(column: Chromatorex C18; 250*30 mm, 10 μM, flow 100 mL/min, gradientacetonitrile/water (containing 0.1% trifluoroacetic acid) 10/90 to 95/5)to yield the desired product (169 mg, 83% purity, 28% yield).

LC-MS (method 11): R_(t)=1.18 min; MS (ESIpos): m/z=473 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.30), −0.008(2.29), 0.008 (2.38), 0.146 (0.29), 0.335 (2.44), 0.346 (2.72), 0.423(0.41), 0.432 (0.54), 0.457 (2.45), 0.476 (2.65), 0.517 (0.37), 1.204(0.35), 1.216 (0.66), 1.223 (0.65), 1.235 (1.04), 1.246 (0.62), 1.254(0.66), 1.266 (0.38), 1.291 (3.69), 1.309 (7.51), 1.326 (3.83), 1.339(1.61), 1.357 (0.72), 2.157 (16.00), 2.261 (2.28), 2.328 (0.67), 2.384(2.44), 2.485 (3.75), 2.671 (0.52), 2.711 (0.24), 2.918 (12.61), 3.047(2.40), 3.926 (2.70), 3.944 (2.63), 3.990 (0.83), 4.007 (0.82), 4.233(1.38), 4.251 (3.54), 4.269 (3.52), 4.286 (1.38), 4.299 (0.94), 4.317(0.88), 4.334 (0.45), 8.126 (3.23), 8.141 (3.33), 8.411 (0.62), 8.429(0.66), 8.535 (0.49), 8.692 (0.69), 8.801 (4.43), 8.818 (4.15), 9.401(0.56), 9.578 (0.69), 9.596 (0.67), 9.675 (0.57).

Intermediate 2332-[5-(1,3-dioxoisoindolin-2-yl)-4-ethyl-3-(4-fluorophenyl)pyrazol-1-yl]acetonitrile

Under an argon atmosphere,2-[4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-1H -isoindole-1,3(2H)-dione (1.63 g, 4.86 mmol) was dissolved in acetonitrile (53 mL) andbromoacetonitrile (510 μl, 7.3 mmol) and cesium carbonate (4.75 g, 14.6mmol) was added. The reaction mixture was stirred for 3.25 h at 60° C.After cooling to ambient temperature, the precipitated salt was removedby filtration and the reaction mixture concentrated to ⅕ of its originalvolume. Water was added and the precipitated solid collected byfiltration and purified by preparative HPLC (column: Chromatorex C18;250*30 mm, 10 μM, flow 100 mL/min, gradient acetonitrile/water(containing 0.1% trifluoroacetic acid) 10/90 to 90/10). Upon standing, asolid precipitated from the filtrate, which was also purified bypreparative HPLC (column: Chromatorex C18; 250*30 mm, 10 μM, flow 100mL/min, gradient acetonitrile/water (containing 0.1% trifluoroaceticacid) 10/90 to 90/10). Product containing fractions were combined andlyophilized to yield the title compound (490 mg, 27% yield) along withthe regioisomeric compound[3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-1-yl]acetonitrile(507 mg, 28% yield).

LC-MS (method 10): Rt=2.04 min; MS (ESIpos): m/z=375 [M+H]⁺

Intermediate 2342-[4-ethyl-3-(4-fluorophenyl)-1-(2H-tetrazol-5-ylmethyl)-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione

Under an argon atmosphere[5-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-1-yl]acetonitrile(350 mg, 935 μmol) and azido(trimethyl)silane (250 μl, 1.9 mmol) weredissolved in toluene (6.7 mL) and di-n-butyltinoxide (46.5 mg, 187 μmol)was added. The reaction mixture was heated to 125° C. bath temperatureovernight. After cooling to ambient temperature, the reaction mixturewas concentrated and the residue purified by flash column chromatography(SNAP Ultra 25 g, dichloromethane/methanol gradient 95/5 to 60/40) toyield the desired product in two fractions: Fraction 1 (213 mg, 74%purity, 40% yield) and fraction 2 (157 mg, 88% purity, 35% yield). Theanalytical data of fraction 2 is given. For the next step, bothfractions were combined and used without further purification.

LC-MS (method 11): R_(t)=1.27 min; MS (ESIpos): m/z=418 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.23), −0.008(1.91), 0.008 (1.67), 0.146 (0.20), 0.807 (0.68), 0.826 (1.62), 0.845(0.75), 0.895 (6.76), 0.914 (16.00), 0.932 (7.02), 1.234 (0.31), 2.220(0.19), 2.239 (0.56), 2.258 (0.54), 2.277 (0.20), 2.327 (0.51), 2.366(0.17), 2.445 (1.85), 2.464 (5.78), 2.483 (6.41), 2.665 (0.38), 2.670(0.52), 2.674 (0.39), 2.710 (0.16), 3.168 (3.75), 5.548 (1.49), 5.678(10.99), 5.754 (1.38), 7.289 (4.19), 7.294 (1.46), 7.311 (8.76), 7.328(1.56), 7.333 (4.69), 7.401 (0.37), 7.423 (0.79), 7.445 (0.46), 7.636(0.44), 7.649 (0.49), 7.658 (0.44), 7.671 (0.41), 7.701 (4.54), 7.706(1.98), 7.714 (5.01), 7.723 (4.69), 7.731 (1.82), 7.737 (4.15), 7.936(0.49), 7.944 (0.54), 7.950 (0.52), 7.957 (0.89), 7.968 (0.63), 7.977(4.69), 7.984 (5.26), 7.991 (4.84), 7.998 (9.00), 8.008 (1.70), 8.019(0.59), 8.029 (1.40), 8.039 (8.48), 8.045 (4.67), 8.052 (5.19), 8.060(4.42), 8.069 (0.41), 16.622 (0.16).

Intermediate 2352-{4-ethyl-3-(4-fluorophenyl)-1-[(2-methyl-2H-tetrazol-5-yl)methyl]-1H-pyrazol-5-yl}-1H-isoindole-1,3(2H)-dione2-[4-ethyl-5-(4-fluorophenyl)-2-[(1-methyltetrazol-5-yl)methyl]pyrazol-3-yl]isoindoline-1,3-dione

2-[4-ethyl-3-(4-fluorophenyl)-1-(2H-tetrazol-5-ylmethyl)-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(212 mg, 508 μmol) and potassium carbonate (140 mg, 1.02 mmol) weresuspended in dimethylformamide (1.0 mL) and methyl iodide was addedunder argon. The reaction mixture was stirred for 3 h at ambienttemperature. Water was added and the reaction mixture was extracted withethyl acetate (2×). The combined organic phase extracts were washed withbrine, dried over sodium sulfate and concentrated. The product mixturethus obtained (211 mg, 87% purity, 84% yield) was a mixture of the tworegioisomers and was used without further purification in the next step.

LC-MS (method 11): R_(t)=1.37 min; MS (ESIpos): m/z=432 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.34), 0.008(2.62), 0.146 (0.33), 0.801 (0.42), 0.819 (0.92), 0.838 (0.50), 0.892(2.70), 0.897 (2.22), 0.910 (6.21), 0.916 (4.74), 0.929 (2.91), 0.934(2.14), 1.074 (0.21), 1.094 (0.37), 1.157 (0.83), 1.175 (1.73), 1.192(0.91), 1.234 (0.68), 1.398 (1.60), 1.988 (3.08), 2.227 (0.26), 2.246(0.35), 2.265 (0.23), 2.328 (0.51), 2.366 (0.19), 2.440 (0.69), 2.459(2.51), 2.478 (3.64), 2.670 (0.63), 2.731 (12.62), 2.890 (16.00), 3.038(1.03), 3.375 (0.37), 3.861 (1.23), 3.926 (1.18), 3.969 (10.10), 4.002(0.27), 4.020 (0.74), 4.038 (0.76), 4.056 (0.25), 4.138 (0.91), 4.184(0.37), 4.219 (13.76), 4.332 (1.47), 4.350 (0.36), 5.483 (0.62), 5.560(6.33), 5.689 (0.54), 5.754 (0.97), 5.775 (4.74), 5.831 (0.43), 7.278(2.55), 7.300 (5.13), 7.322 (2.76), 7.402 (0.36), 7.418 (0.30), 7.440(0.20), 7.612 (0.36), 7.634 (0.28), 7.671 (1.52), 7.681 (2.21), 7.685(2.24), 7.694 (2.83), 7.703 (2.24), 7.706 (1.53), 7.717 (1.61), 7.952(2.08), 7.984 (2.80), 7.992 (3.25), 7.998 (3.47), 8.006 (5.02), 8.017(1.05), 8.043 (0.85), 8.053 (5.13), 8.060 (3.15), 8.066 (3.36), 8.074(2.81).

Intermediate 2364-ethyl-3-(4-fluorophenyl)-1-[(1-methyl-1H-tetrazol-5-yl)methyl]-1H-pyrazol-5-amine

The mixture of regioisomers2-{4-ethyl-3-(4-fluorophenyl)-1-[(2-methyl-2H-tetrazol-5-yl)methyl]-1H-pyrazol-5-yl}-1H-isoindole-1,3(2H)-dioneand2-[4-ethyl-5-(4-fluorophenyl)-2-[(1-methyltetrazol-5-yl)methyl]pyrazol-3-yl]isoindoline-1,3-dione(210 mg, 487 μmol) was suspended in ethanol and hydrazine monohydrate(120 μL, 2.4 mmol) was added. The reaction mixture was refluxed for 3 hand cooled to ambient temperature. The reaction mixture was diluted withwater and extracted with ethyl acetate (2×). The combined organic phaseextracts were washed with brine, dried over sodium sulfate andconcentrated. The residue was dissolved in methanol (14 mL) purified bypreparative SFC (Daciel Chiralpak AY-H 5 μm, 250×20 mm, flow: 80 mL/min,40° C., isocratic carbon dioxide/ethanol 78/22, injections of 0.5 mLevery 6 min) to yield the title compound (28.7 mg, 18% yield) as thefirst eluting isomer (R_(t)=2.84 min) along with the regioisomer (seebelow).

LC-MS (method 11): R_(t)=1.08 min; MS (ESIpos): m/z=302 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.008 (0.43), 0.979(2.48), 0.998 (5.91), 1.016 (2.59), 1.235 (0.24), 2.328 (0.20), 2.366(0.16), 2.414 (0.76), 2.432 (2.29), 2.451 (2.27), 2.470 (0.77), 2.670(0.22), 3.038 (0.18), 3.860 (0.18), 4.011 (16.00), 5.237 (3.73), 5.552(7.90), 5.754 (3.63), 7.174 (1.63), 7.196 (3.43), 7.218 (1.87), 7.506(1.90), 7.511 (0.77), 7.520 (2.12), 7.528 (1.94), 7.537 (0.70), 7.542(1.70).

Intermediate 2374-ethyl-3-(4-fluorophenyl)-1-[(2-methyl-2H-tetrazol-5-yl)methyl]-1H-pyrazol-5-amine

The title compound was obtained during the synthesis of4-ethyl-3-(4-fluorophenyl)-1-[(1-methyl-1H-tetrazol-5-yl)methyl]-1H-pyrazol-5-amine(see above) after purification by preparative SFC (Daciel Chiralpak AY-H5 μm, 250×20 mm, flow: 80 mL/min, 40° C., isocratic carbondioxide/ethanol 78/22, injections of 0.5 mL every 6 min) as the secondeluting isomer (R_(t)=4.30 min, 41 mg, 25% yield).

LC-MS (method 11): R_(t)=1.08 min; MS (ESIpos): m/z=302 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.989 (2.55), 1.004(5.88), 1.019 (2.58), 2.426 (0.73), 2.440 (2.32), 2.455 (2.24), 2.470(0.73), 4.335 (16.00), 5.116 (4.01), 5.425 (7.36), 7.168 (1.72), 7.173(0.60), 7.182 (0.83), 7.186 (3.51), 7.190 (0.73), 7.200 (0.65), 7.204(1.89), 7.513 (1.89), 7.517 (0.78), 7.524 (2.09), 7.531 (1.89), 7.538(0.74), 7.542 (1.64).

Intermediate 238 ethyl (2E)-(2-methylhydrazinylidene)ethanoate

Ethyl oxoacetate (20 ml, 50% purity, 98 mmol) was dissolved intetrahydrofuran (28 mL) and cooled to 0° C. Methylhydrazine (5.3 ml, 100mmol) was added dropwise and the reaction mixture stirred for 30 min at0° C. and overnight at ambient temperature. The reaction mixture wasconcentrated and the residue redissolved in toluene and concentratedagain (3 cycles). The residue was triturated with methyl tert-butyletherand stirred 30 min at 0° C. The precipitated solid was collected byfiltration, washed with ice-cold methyl tert-butylether and dried toyield the desired product (9.47 g, 74% yield).

LC-MS (method 9): R_(t)=0.42 min; MS (ESIpos): m/z=131 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.72), 0.008(0.62), 1.186 (7.81), 1.203 (16.00), 1.221 (7.96), 2.788 (11.05), 2.798(10.89), 3.264 (0.42), 4.076 (2.62), 4.094 (7.93), 4.112 (7.85), 4.130(2.57), 6.534 (4.89), 8.811 (1.16).

Intermediate 239 ethyl5-(4-fluorophenyl)-4-hydroxy-1-methyl-1H-pyrazole-3-carboxylate

Under an argon atmosphere, ethyl (2E)-(2-methylhydrazinylidene)ethanoate(9.17 g, 70.5 mmol) was dissolved in n-butyl acetate (270 mL) and thesolution cooled to 0° C. (4-fluorophenyl)(oxo)acetaldehyde monohydrate(24.0 g, 141 mmol), magnesium sulfate (18.2 g, 150 mmol) and acetic acid(9.1 mL, 160 mmol) were added and the reaction mixture was allowed towarm to ambient temperature and was stirred for 20 min. It was thenheated to 110° C. for 1 h. After cooling to ambient temperature, thesolids were removed by filtration and washed with with ethyl acetate.The filtrate was concentrated and triturated with methyltert-butylether. The precipitated solid was collected by filtration andwashed further with methyl tert-butylether to yield the desired productas a white solid (14.0 g, 75% yield).

LC-MS (method 9): R_(t)=0.85 min; MS (ESIpos): m/z=265 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.51), 0.008(0.48), 1.279 (4.04), 1.296 (8.61), 1.314 (4.15), 3.791 (16.00), 4.258(1.32), 4.276 (4.09), 4.293 (4.05), 4.311 (1.27), 7.332 (1.74), 7.337(0.65), 7.348 (0.86), 7.354 (3.89), 7.371 (0.71), 7.376 (2.23), 7.540(2.19), 7.546 (0.96), 7.554 (2.40), 7.562 (2.07), 7.571 (0.82), 7.576(1.82), 8.391 (4.21).

Intermediate 240 ethyl4-(difluoromethoxy)-5-(4-fluorophenyl)-1-methyl-1H-pyrazole-3-carboxylate

Under an argon atmosphere, potassium hydroxide (26.4 g, 470 mmol) wasdissolved in water (120 mL) and the resulting solution treated withacetonitrile (120 mL). When the mixture became homogeneous, was cooledto ca. −30° C. (as low as stirring is still possible). ethyl5-(4-fluorophenyl)-4-hydroxy-1-methyl-1H-pyrazole-3-carboxylate (6.21 g,23.5 mmol) was added as as a solid, followed by dropwise addition ofdiethyl [bromo(difluoro)methyl]phosphonate (8.3 ml, 47 mmol) over 5 min.After 15 min, the reaction mixture was neutralized with aqueoushydrochloric acid solution (2 N, 100 mL) and extracted with methyltert-butylether (3×). The combined organic phase extracts were washedwith brine, dried over sodium sulfate and concentrated. The desiredproduct thus obtained (7.87 g, 92% purity, 98% yield) was used in thenext step without further purification.

¹H NMR (500 MHz, dimethylsulfoxide-d₆) δ ppm: 1.30 (t, J=7.1 Hz, 3H),3.80 (s, 3H), 4.25-4.37 (m, 2H), 6.76-7.15 (m, 1H), 7.35-7.46 (m, 2H),7.51-7.63 (m, 2H).

Intermediate 2414-(difluoromethoxy)-5-(4-fluorophenyl)-1-methyl-1H-pyrazole-3-carboxylicacid

Ethyl 4-(difluoromethoxy)-5-(4-fluorophenyl)-1-methyl-1H-pyrazole-3-carboxy late (7.87 g, 83% purity, 20.8 mmol) was dissolved intetrahydrofuran/methanol (6:1, 141 mL) and sodium hydroxide solution(100 ml, 1.0 M, 100 mmol) was added. The reaction mixture was stirredfor 2 h at ambient temperature. It was then acidified by addition ofaqueous hydrochloric acid solution (2 N) and extracted withdichloromethane (3×). The combined organic phase extracts were washedwith brine, dried over sodium sulfate and concentrated. The product thusobtained (6.11 g, 98% yield) was used in the next step without furtherpurification.

LC-MS (method 10): Rt=1.47 min; MS (ESIneg): m/z=285 [M−H]⁻

Intermediate 242 tert-butyl[4-(difluoromethoxy)-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]carbamate

This reaction was carried out behind a safety explosion shield! Under anargon atmosphere (argon flow, open reaction vessel, no bubbler),4-(difluoromethoxy)-5-(4-fluorophenyl)-1-methyl-1H-pyrazole-3-carboxylicacid (1.33 g, 95% purity, 4.41 mmol) and triethylamine (860 μl, 6.2mmol) were dissolved in toluene and diphenyl phosphorazidate (1.1 ml,5.3 mmol) was added. The reaction mixture was stirred for 1 h at ambienttemperature, when tert-butanol (20 ml, 210 mmol) was added. The reactionmixture was then heated to 80° C. overnight. After cooling to ambienttemperature, water (3 mL) and a solution of trimethylphosphine (7.1 ml,1.0 M, 7.1 mmol) was added. The reaction mixture was stirred for 1 h atambient temperature. It was then diluted with saturated aqueous sodiumhydrogencarbonate solution and extracted with ethyl acetate (3×). Thecombined organic phase extracts were washed with saturated aqueouessodium hydrogencarbonate solution and brine, dried over sodium sulfateand concent rated. The desired product thus obtained (1.81 g, 72%purity, 83% yield) was used in the next step without furtherpurification.

LC-MS (method 11): R_(t)=1.32 min; MS (ESIneg): m/z=356 [M−H]⁻

¹H NMR (400 MHz, dimethylsulfoxide-d₆) δ ppm: 1.43 (s, 9H), 3.66 (s,3H), 6.51-6.93 (t, J=74 Hz, 1H), 7.33-7.44 (m, 2H), 7.49-7.61 (m, 2H),8.88-8.96 (m, 1H).

Intermediate 2434-(difluoromethoxy)-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine

Tert-butyl[4-(difluoromethoxy)-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]carbamate(1.81 g, 5.07 mmol) was dissolved in dichloromethane (10 mL) andtrifluoroacetic acid (10 mL) was added. The reaction mixture was stirredat ambient temperature for 1 h. The reaction mixture was concentratedand the residue resuspended in dichloromethane and again concentrated (3cycles). The residue was dissolved in acetonitrile/water and purified bypreparative HPLC (column: Chromatorex C18; 200*40 mm, 10 μM, flow 100mL/min, gradient acetonitrile/water (containing 0.1% trifluoroaceticacid) 10/90 to 90/10) to yield the desired product (609 mg, 46% yield).

LC-MS (method 11): R_(t)=1.04 min; MS (ESIpos): m/z=

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 3.49 (s, 3H), 4.63-4.70(m, 2H), 6.71 (t, J=75.4 Hz, 1H), 7.31-7.39 (m, 2H), 7.44-7.52 (m, 2H).

Intermediate 2444-(5-{[6-(4-formyl-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-1,4-dimethyl-1H-pyrazol-3-yl)benzonitrile

A microwave vial was charged1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbaldehyde (625mg, 85% purity, 2.24 mmol) and4-(5-amino-1,4-dimethyl-1H-pyrazol-3-yl)benzonitrile (524 mg, 2.47 mmol)and the contents were suspended in 1,4-dioxane (6.5 ml, 76 mmol). Thereaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (61.7 mg, 67.3 μmol) and Xantphos(77.9 mg, 135 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (287 mg, 2.47 mmol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with hydrochloricacid and extracted with ethyl acetate (2×). The combined organic phaseswere washed with water and brine, dried over sodium sulfate andconcentrated under reduced pressure. The crude product was suspended inacetonitrile and left overnight. The occurring precipitate was collectedby filtration washed with acetonitrile and dried to yield 300 mg (31%)of the desired product.

LC-MS (method 10): R_(t)=1.74 min; MS (ESIpos): m/z=413 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.052 (0.44), 2.080(13.39), 2.471 (1.17), 2.941 (11.95), 2.959 (0.73), 3.014 (0.96), 3.481(0.74), 3.570 (1.22), 7.340 (0.73), 7.380 (0.75), 7.460 (0.98), 7.464(1.09), 7.477 (0.83), 7.488 (0.48), 7.780 (0.48), 7.793 (0.50), 7.812(0.44), 7.820 (0.54), 7.896 (16.00), 8.559 (0.62), 9.685 (1.44), 10.017(3.25), 10.059 (0.42).

Intermediate 245 ethyl[1-(6-{[1-(4-fluorophenyl)-3,5-dimethyl-1H-pyrazol-4-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]acetate

A microwave vial was charged ethyl[1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]acetate (255mg, 866 μmol), 1-(4-fluorophenyl)-3,5-dimethyl-1H-pyrazol-4-amine (230mg, 85% purity, 953 μmol) and sodium phenolate (111 mg, 953 μmol) andthe contents were suspended in 1,4-dioxane (4.2 ml, 49 mmol). Thereaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (10.3 mg, 11.3 μmol) and Xantphos(15.0 mg, 26.0 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was filtered and purified by preparative HPLC (method:column: Reprosil C18; 10 μm; 125×40 mm/flow: 75 mL/min/solvent: A=water(0.1% formic acid), B=acetonitrile/gradient: 0.00-5.50 min=10% B,17.65-19.48 min=95% B, 19.66 min=10% B) to yield the desired product(85.0 mg, 19%).

LC-MS (method 10): R_(t)=1.96 min; MS (ESIpos): m/z=464 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.165 (3.44), 1.183(7.00), 1.200 (3.53), 1.647 (0.58), 1.999 (1.51), 2.077 (16.00), 2.121(3.22), 2.177 (11.00), 2.564 (13.98), 3.468 (4.41), 4.047 (1.02), 4.065(3.01), 4.082 (2.98), 4.100 (1.00), 7.300 (0.41), 7.333 (1.70), 7.355(3.56), 7.377 (2.18), 7.397 (0.61), 7.592 (1.54), 8.401 (0.62), 8.867(2.24).

Intermediate 2463-[4-(difluoromethyl)phenyl]-4-methyl-1H-pyrazol-5-amine

A solution of 3-[4-(difluoromethyl)phenyl]-2-methyl-3-oxopropanenitrile(1.45 g, 6.92 mmol) in ethanol (15 ml) was treated with 8B] and stirredat 95° C. overnight. After cooling to ambient temperature the mixturewas purified by preparative HPLC (method: column: Reprosil C18; 10 μm;125×30 mm/flow: 50 mL/min/solvent: A=water (0.01% formic acid),B=acetonitrile/gradient: 0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75min=100% B, 19.75-23.00 min=90% B) to yield 1.44 g (86.7%) of thedesired product.

LC-MS (method 10): R_(t)=1.11 min; MS (ESIpos): m/z=224 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.004 (16.00), 4.579(0.44), 6.906 (1.13), 7.046 (2.28), 7.186 (1.05), 7.601 (2.04), 7.621(3.71), 7.666 (3.98), 7.686 (2.10).

Intermediate 2472-{3-[4-(difluoromethyl)phenyl]-4-methyl-1H-pyrazol-5-yl}-1H-isoindole-1,3(2H)-dione

A solution of 3-[4-(difluoromethyl)phenyl]-4-methyl-1H-pyrazol-5-amine(765 mg, 3.43 mmol) and 2-benzofuran-1,3-dione (761 mg, 5.14 mmol) inacetic acid (5.0 ml, 87 mmol) was stirred overnight at 140° C. Aftercooling to ambient temperature the mixture was diluted with water. Theoccurring precipitate was collected by filtration, washed with water anddried to yield 1.12 g (92%) of the desired product.

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.912 (0.79), 2.046(16.00), 2.083 (1.98), 3.328 (1.01), 6.972 (2.11), 7.112 (4.41), 7.252(1.89), 7.724 (2.90), 7.744 (5.10), 7.789 (5.02), 7.809 (2.93), 7.885(0.45), 7.904 (0.55), 7.946 (3.81), 7.954 (4.61), 7.960 (4.98), 7.968(7.03), 7.978 (1.55), 8.003 (1.33), 8.012 (5.98), 8.020 (4.71), 8.026(4.48), 8.034 (3.55), 8.053 (0.85), 8.073 (0.67), 10.072 (1.23), 13.517(2.37).

Intermediate 2482-{3-[4-(difluoromethyl)phenyl]-1,4-dimethyl-1H-pyrazol-5-yl}-1H-isoindole-1,3(2H)-dione

A solution of2-{3-[4-(difluoromethyl)phenyl]-4-methyl-1H-pyrazol-5-yl}-1H-isoindole-1,3(2H)-dione(1.82 g, 5.15 mmol) in dimethylformamide (16 ml, 210 mmol) was treatedwith cesium carbonate (3.36 g, 10.3 mmol) and iodomethane (640 μl, 10mmol). The mixture was stirred overnight at ambient temperature. Themixture was poured into saturated ammonium chloride solution. Theoccurring precipitate was collected by filtration, dried and purified byflash-chromatography (column: SNAP Ultra 50 g/solvent: 99%dichloromethane/1% ethyl acetate to 13% ethyl acetate) to yield 404 mgof the desired product (21%) along with its regioisomer.

LC-MS (method 10): R_(t)=1.88 min; MS (ESIpos): m/z=368 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.851 (16.00), 1.990(0.66), 3.317 (10.47), 7.006 (1.16), 7.146 (2.41), 7.285 (1.05), 7.687(2.38), 7.708 (4.32), 7.754 (4.01), 7.774 (2.22), 7.939 (2.04), 7.947(2.38), 7.953 (2.57), 7.961 (3.77), 7.971 (0.74), 7.996 (0.67), 8.006(3.89), 8.014 (2.62), 8.019 (2.50), 8.027 (2.08).

Intermediate 2492-{5-[4-(difluoromethyl)phenyl]-1,4-dimethyl-1H-pyrazol-3-yl}-1H-isoindole-1,3(2H)-dione

A solution of2-{3-[4-(difluoromethyl)phenyl]-4-methyl-1H-pyrazol-5-yl}-1H-isoindole-1,3(2H)-dione(1.82 g, 5.15 mmol) in dimethylformamide (16 ml, 210 mmol) was treatedwith cesium carbonate (3.36 g, 10.3 mmol) and iodomethane (640 μl, 10mmol). The mixture was stirred overnight at ambient temperature. Themixture was poured into saturated ammonium chloride solution. Theoccurring precipitate was collected by filtration, dried and purified byflash-chromatography (column: SNAP Ultra 50 g/solvent: 99%dichloromethane/1% ethyl acetate to 13% ethyl acetate) to yield 314 mgof the desired product (17%) along with its regioisomer.

LC-MS (method 10): R_(t)=1.96 min; MS (ESIpos): m/z=368 [M+H]⁺

Intermediate 2503-[4-(difluoromethyl)phenyl]-1,4-dimethyl-1H-pyrazol-5-amine

A solution of2-{3-[4-(difluoromethyl)phenyl]-1,4-dimethyl-1H-pyrazol-5-yl}-1H-isoindole-1,3(2H)-dione (400 mg, 1.09 mmol) in ethanol (10 mL) was treated withhydrazine monohydrate (265 μL, 5.4 mmol) and stirred at 90° C.overnight. After cooling to ambient temperature the mixture was dilutedwith water and extracted with ethyl acetate (3×). The combined organicphases were washed with saturated sodium hydrogen carbonate solution andbrine, dried over sodium sulfate and concentrated under reduced pressureto yield 263 mg (77%) of the desired product.

LC-MS (method 9): R_(t)=0.69 min; MS (ESIpos): m/z=238 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.790 (16.00), 4.495(3.95), 6.961 (1.16), 7.100 (2.33), 7.240 (1.11), 7.492 (3.46), 7.512(4.19), 7.675 (4.01), 7.695 (3.31).

Intermediate 2515-[4-(difluoromethyl)phenyl]-1,4-dimethyl-1H-pyrazol-3-amine

A solution of2-{5-[4-(difluoromethyl)phenyl]-1,4-dimethyl-1H-pyrazol-3-yl}-1H-isoindole-1,3(2H)-dione (300 mg, 817 μmol) in ethanol (10 mL) was treated withhydrazine monohydrate (199 μL, 4.1 mmol) and stirred at 90° C.overnight. After cooling to ambient temperature the mixture was dilutedwith saturated sodium hydrogen carbonate solution and extracted withethyl acetate (3×). The combined organic phases were washed withsaturated sodium hydrogen carbonate solution and brine, dried oversodium sulfate and concentrated under reduced pressure to yield 186 mg(90%) of the desired product.

LC-MS (method 9): R_(t)=0.67 min; MS (ESIpos): m/z=238 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.017 (16.00), 3.320(3.68), 4.995 (4.91), 6.886 (1.07), 7.026 (2.15), 7.166 (1.00), 7.546(2.56), 7.566 (3.25), 7.707 (3.65), 7.727 (2.82).

Intermediate 2524-[3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-methoxy-1H-pyrazol-5-yl]benzonitrile

A solution of 4-(3-amino-4-methoxy-1H-pyrazol-5-yl)benzonitrile (9.00 g,42.0 mmol) and 2-benzofuran-1,3-dione (9.33 g, 63.0 mmol) in acetic acid(120 ml) was stirred at 125° C. overnight. After cooling to roomtemperature the mixture was concentrated under reduced pressure, theremaining residue was diluted with water and extracted with ethylacetate (3×). The combined organic phases were washed with water andbrine, dried over sodium sulfate and concentrated under reduced pressureto yield 17.0 g (quant.) of the desired crude product.

LC-MS (method 9): R_(t)=0.89 min; MS (ESIpos): m/z=345 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.909 (0.49), 1.988(0.47), 2.053 (0.43), 2.075 (1.90), 3.170 (0.79), 3.319 (1.33), 3.641(2.16), 3.663 (13.07), 3.714 (0.78), 7.572 (1.52), 7.580 (1.71), 7.586(1.86), 7.594 (2.46), 7.604 (0.46), 7.661 (1.86), 7.670 (1.53), 7.675(1.52), 7.684 (1.19), 7.871 (0.44), 7.892 (0.60), 7.972 (4.39), 7.996(16.00), 8.019 (3.30), 8.042 (5.43), 8.049 (4.80), 8.062 (3.46), 8.081(1.80), 8.089 (1.35), 8.094 (1.37), 8.102 (0.98), 13.770 (1.58).

Intermediate 2534-[5-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-methoxy-1-methyl-1H-pyrazol-3-yl]benzonitrile

A solution of4-[3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-methoxy-1H-pyrazol-5-yl]benzonitrile(17.0 g, 49.4 mmol) in dimethylformamide (150 ml, 2.0 mol) was treatedwith cesium carbonate (32.2 g, 98.7 mmol) and iodomethane (6.1 ml, 99mmol). The mixture was stirred overnight. The mixture was filtered andpoured into saturated ammonium chloride solution. The occurringprecipitate was collected by filtration, washed with water and dried.The crude product was purified by flash-chromatography (column; SNAPUltra 100 g, solvent: dichloromethane/ethyl acetate 40:1) to yield 8.50g (45%) of the desired product along with its regioiomer.

LC-MS (method 10): R_(t)=1.87 min; MS (ESIpos): m/z=359 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 3.313 (14.52), 3.653(16.00), 7.906 (2.79), 7.928 (3.98), 7.997 (1.95), 8.004 (2.16), 8.010(2.23), 8.018 (3.16), 8.029 (4.58), 8.051 (2.95), 8.072 (0.44), 8.082(3.00), 8.089 (2.10), 8.096 (2.08), 8.103 (1.84).

Intermediate 2544-[3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-methoxy-1-methyl-1H-pyrazol-5-yl]benzonitrile

A solution of 4-[3-(1,3-dioxo-1,3-dihy dro-2H-isoindol-2-yl)-4-methoxy-1H-pyrazol-5-yl]benzonitrile (17.0 g, 49.4 mmol) in dimethylformamide(150 ml, 2.0 mol) was treated with cesium carbonate (32.2 g, 98.7 mmol)and iodomethane (6.1 ml, 99 mmol). The mixture was stirred overnight.The mixture was filtered and poured into saturated ammonium chloridesolution. The occurring precipitate was collected by filtration, washedwith water and dried. The crude product was purified byflash-chromatography (column; SNAP Ultra 100 g, solvent:dichloromethane/ethyl acetate 40:1) to yield 2.62 g (15%) of the desiredproduct along with its regioiomer.

LC-MS (method 10): R_(t)=1.70 min; MS (ESIpos): m/z=359 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 3.315 (8.51), 3.505(16.00), 7.822 (2.98), 7.843 (3.54), 7.962 (1.65), 7.970 (1.86), 7.975(1.92), 7.983 (2.88), 7.993 (0.52), 8.031 (4.55), 8.038 (2.29), 8.045(3.19), 8.049 (3.38).

Intermediate 2554-(5-amino-4-methoxy-1-methyl-1H-pyrazol-3-yl)benzonitrile

A solution of4-[5-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-methoxy-1-methyl-1H-pyrazol-3-yl]benzonitrile(8.50 g, 23.7 mmol) in ethanol (260 ml, 4.4 mol) was treated withhydrazine monohydrate (5.8 ml, 120 mmol) and stirred at 90° C.overnight. After cooling to ambient temperature the mixture was dilutedwith water and extracted with ethyl acetate (3×). The combined organicphases were washed with saturated sodium hydrogen carbonate solution andbrine, dried over sodium sulfate and concentrated under reduced pressureto yield 5.85 g (quant.) of the desired product.

LC-MS (method 10): R_(t)=1.15 min; MS (ESIpos): m/z=229 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 3.317 (4.36), 3.634(16.00), 5.163 (3.96), 7.801 (3.08), 7.817 (1.33), 7.822 (4.15), 7.949(4.22), 7.966 (1.18), 7.970 (3.09).

Intermediate 2564-(3-amino-4-methoxy-1-methyl-1H-pyrazol-5-yObenzonitrile

A solution of4-[3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-methoxy-1-methyl-1H-pyrazol-5-yl]benzonitrile(2.62 g, 7.31 mmol) in ethanol (100 ml, 1.7 mol) was treated withhydrazine monohydrate (1.8 ml, 37 mmol) and stirred at 90° C. overnight.After cooling to ambient temperature the mixture was diluted with waterand extracted with ethyl acetate (3×). The combined organic phases werewashed with saturated sodium hydrogen carbonate solution and brine,dried over sodium sulfate and concentrated under reduced pressure toyield 1.62 g (97%) of the desired product.

LC-MS (method 10): R_(t)=1.07 min; MS (ESIpos): m/z=229 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.075 (0.47), 3.316(16.00), 4.643 (11.51), 7.654 (9.72), 7.658 (3.74), 7.675 (11.10), 7.941(11.15), 7.962 (9.25).

Intermediate 2576-chloro-N-[1-(cyclopropylmethyl)-3-(4-fluoronphenyl)-4-methyl-4-methyl-1H-pyrazol-5-yl]pyrimidin-4-amine

A solution of 4,6-dichloropyrimidine (128 mg, 856 μmol) and1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine(210 mg, 856 μmol) in dimethylformamide (4.0 ml, 52 mmol) was treatedwith dimethylformaimde (4 mL) and sodium iodide (154 mg, 1.03 mmol) andstirred two days at 125° C. After cooling to room temperature themixture was purified by preparative HPLC (method: column: Reprosil C18;10 μm; 125×40 mm/flow: 75 mL/min/solvent: A=water (0.1% formic acid),B=acetonitrile/gradient: 0.00-5.50 min=10% B, 17.65-19.48 min=95% B,19.66 min=10% B) to yield 85.0 mg of the desired product (28%).

LC-MS (method 10): R_(t)=1.93 min; MS (ESIpos): m/z=358 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.272 (0.73), 0.281(0.77), 0.415 (0.87), 0.435 (0.93), 1.165 (0.41), 1.981 (6.27), 3.568(16.00), 3.807 (0.87), 3.824 (0.84), 7.244 (0.93), 7.267 (1.95), 7.289(1.03), 7.703 (0.60), 7.718 (0.75), 7.724 (0.74), 7.739 (0.57).

Intermediate 258N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-hydrazinylpyrimidin-4-amine

A solution of6-chloro-N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]pyrimidin-4-amine(83.2 mg, 233 μmol) in 1,4-dioxane (1.5 ml) was treated with hydrazinehydrate (1:1) (34 μl, 700 μmol) and stirred overnight at 70° C. As theconversion was not fully completed additional 3 equivalents of hydrazinemonohydrate (34 μL, 697 μmol) were added and it was stirred anadditional night at 70° C. After cooling to room temperature a thirdtime 6 equivalents of hydrazine monohydrate (68 μL, 1.39 mmol) wereadded and stirring was continued at 70° C. for 3 days. The mixture wasconcentrated under reduced pressure to yield 95.0 mg (81%) of thedesired product.

LC-MS (method 11): R_(t)=0.87 min; MS (ESIneg): m/z=352 [M−H]⁻

Intermediate 2594-chloro-6-(3,5-dimethyl-4-nitro-1H-pyrazol-1-yl)pyrimidine

4,6-Dichloropyrimidine (2.22 g, 14.9 mmol),3,5-dimethyl-4-nitro-1H-pyrazole (2.00 g, 14.2 mmol) and cesiumcarbonate (4.62 g, 14.2 mmol) were suspended in dimethylformamide (9 mL)and the reaction mixture was stirred for 2.5 h at ambient temperature.It was then poured onto water and stirred for further 5 min. Theprecipitated solid was collected by filtration, further washed withwater and dried in a vacuum drying-oven at 40° C. overnight. The desiredproduct thus obtained (2.98 g, 67% purity, 53% yield) was used in thenext step without further purification.

LC-MS (method 11): Rt=1.32 min; MS (ESIpos): m/z=254 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.525 (15.69), 3.029(16.00), 3.087 (9.88), 8.077 (3.32), 8.079 (3.24), 8.309 (1.11), 8.311(1.09), 9.091 (2.92), 9.093 (2.82), 9.220 (1.09), 9.222 (1.05).

Intermediate 260 ethyl 5-fluoropyridine-2-carboxylate hydrochloride

5-fluoropyridine-2-carboxylic acid (5.00 g, 35.4 mmol) was suspended inthionyl chloride (15 ml, 210 mmol) and refluxed for 30 minutes. Aftercooling to room temperature the mixture was concentrated under reducedpressure. The remaining residue was resolved in ethanol and refluxed fortwo hours. After cooling to ambient temperature the mixture wasconcentrated, the residue was suspended in diethyl ether and theoccurring crystalline material was collected by filtration, washed withdiethyl ether and dried to yield 4.20 g (58%) of the desired product.

LC-MS (method 10): R_(t)=1.10 min; MS (ESIpos): m/z=170 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.006 (2.46), 1.322(7.79), 1.336 (16.00), 1.351 (7.74), 4.331 (2.56), 4.345 (7.69), 4.359(7.52), 4.374 (2.39), 7.900 (1.30), 7.906 (1.35), 7.918 (2.64), 7.924(2.67), 7.935 (1.48), 7.941 (1.48), 8.143 (2.14), 8.152 (2.15), 8.161(1.88), 8.170 (1.79), 8.716 (3.64), 8.722 (3.45).

Intermediate 261 3-(5-fluoropyridin-2-yl)-2-methyl-3-oxopropanenitrile

A solution of ethyl 5-fluoropyridine-2-carboxylate hydrochloride (1:1)(6.15 g, 29.9 mmol) and propanenitrile (3.2 ml, 45 mmol) intetrahydrofuran (76 ml, 940 mmol) was treated with a solution of lithiumbis(trimethylsilyl)amide (76 ml, 1.0 M in tetrahydrofuran, 76 mmol). Themixture was stirred overnight at ambient temperature. The mixture wasdiluted with water and extracted once with ethyl acetate. The organicphase was discarded. The aqueous phase was acidified with hydrochloricacid and extracted with dichloromethane (2×). The combined organicphases were washed with water, dried over sodium sulfate andconcentrated under reduced pressure to yield 4.15 g (61%) of the desiredproduct.

LC-MS (method 9): R_(t)=0.71 min; MS (ESIpos): m/z=179 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.508 (15.88), 1.526(16.00), 1.785 (1.31), 1.910 (8.45), 5.111 (1.32), 5.129 (3.96), 5.148(3.92), 5.166 (1.28), 7.861 (1.55), 7.873 (1.88), 7.890 (1.31), 7.974(1.26), 7.980 (1.31), 7.996 (2.67), 8.002 (2.67), 8.017 (1.61), 8.023(1.52), 8.119 (0.59), 8.131 (0.59), 8.142 (0.40), 8.160 (2.82), 8.172(2.93), 8.182 (2.38), 8.193 (2.19), 8.619 (0.41), 8.625 (0.41), 8.693(2.10), 8.807 (4.74), 8.812 (4.53).

Intermediate 2621-(cyclopropylmethyl)-3-(5-fluoropyridin-2-yl)-4-methyl-1H-pyrazol-5-amine

A solution of 3-(5-fluoropyridin-2-yl)-2-methyl-3-oxopropanenitrile(1.50 g, 8.42 mmol) in ethanol (18 ml) was treated with(cyclopropylmethyl)hydrazine dihydrochloride (2.68 g, 16.8 mmol) andstirred overnight at 95° C. The mixture was purified by preparative HPLC(method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent:A=water (0.01% formic acid), B=acetonitrile/gradient: 0.00-5.00 min=10%B, 6.50 min=20% B, 17.0-19.75 min=100% B, 19.75-23.00 min=90% B) toyield 908 mg (44%) of the desired product as mixture with unknownby-products.

LC-MS (method 10): R_(t)=1.25 min; MS (ESIpos): m/z=247 [M+H]⁺

Intermediate 2634-(5-{[6-(4-formyl-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-4-methoxy-1-methyl-1H-pyrazol-3-yl)benzonitrile

A microwave vial was charged1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbaldehyde (300mg, 76% purity, 963 μmol) and4-(5-amino-4-methoxy-1-methyl-1H-pyrazol-3-yl)benzonitrile (242 mg, 1.06mmol) and the contents were suspended in 1,4-dioxane (3.5 ml, 41 mmol).The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (26.5 mg, 28.9 μmol) and Xantphos(33.4 mg, 57.8 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (123 mg, 1.06 mmol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was left overnight and waspurified by preparative HPLC (method: column^(.) Reprosil C18; 10 μm;125×30 mm/flow: 50 mL/min/solvent: A=water (0.01% formic acid),B=acetonitrile/gradient: 0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75min=100% B, 19.75-23.00min=90% B) to yield the desired product (135 g,31%).

LC-MS (method 10): R_(t)=1.75 min; MS (ESIpos): m/z=429 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.647 (0.66), 2.447(1.99), 2.948 (16.00), 2.971 (1.74), 3.316 (9.14), 3.630 (0.64), 3.662(14.64), 3.702 (0.64), 5.755 (6.78), 7.366 (0.56), 7.382 (0.63), 7.396(0.63), 7.870 (4.51), 7.890 (5.78), 8.030 (6.18), 8.051 (4.92), 8.590(2.28), 9.028 (0.42), 9.709 (1.79), 10.019 (5.08), 10.050 (0.61).

Intermediate 264 ethyl[1-(6-{[3-(4-cyanophenyl)-4-methoxy-1-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]acetate

A microwave vial was charged ethyl[1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]acetate (117mg, 398 μmol) and4-(5-amino-4-methoxy-1-methyl-1H-pyrazol-3-yl)benzonitrile (100 mg, 438μmol) and the contents were suspended in 1,4-dioxane (6.0 ml, 70 mmol).The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (10.9 mg, 11.9 μmol) and Xantphos(13.8 mg, 23.9 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (50.9 mg, 438 μmol) was added. The vial was sealed and heatedat 85° C. for 6 hours while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with hydrochloricacid and extracted with ethyl acetate (2×). The combined organic phaseswere washed with water and brine, dried over sodium sulfate andconcentrated under reduced pressure. The crude product was purified byflash-chromatography (column: SNAP Ultra 10 g, solvent:dichloromethane/ethyl acetate 80:20) to yield the desired product (80.0mg, 36%).

LC-MS (method 10): R_(t)=1.98 min; MS (ESIpos): m/z=487 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.171 (3.32), 1.185(6.90), 1.199 (3.36), 2.143 (2.44), 2.588 (10.58), 3.485 (3.99), 3.581(2.38), 3.636 (2.81), 3.656 (6.30), 3.730 (16.00), 4.057 (0.95), 4.071(2.86), 4.086 (2.83), 4.100 (0.91), 5.754 (2.09), 7.802 (0.49), 7.820(0.64), 7.871 (2.76), 7.874 (1.12), 7.884 (1.27), 7.888 (3.43), 7.952(0.63), 7.969 (0.50), 8.037 (2.99), 8.054 (2.35), 8.503 (0.95), 9.521(1.11).

Intermediate 265 4-(cyanoacetyl)benzonitrile

A solution of ethyl 4-cyanobenzoate (5.00 g, 28.5 mmol) intetrahydrofuran (38 ml, 470 mmol) was treated with potassiumtert-butoxide (6.41 g, 57.1 mmol). The mixture was stirred for 5 minutesat ambient temperature and then acetonitrile (1.5 ml, 29 mmol) wasadded. The reaction mixture was stirred two hours at ambienttemperature. The mixture was diluted with hydrochloric acid (2.0 M)under ice bath cooling and extracted with ethyl acetate (2×). Thecombined organic phases were dried over sodium sulfate and concentratedunder reduced pressure. The remaining residue was suspended in diethylether; the occurring precipitate was collected by filtration, washedwith diethyl ether and dried to yield 4.24 g (87%) of the desiredproduct.

LC-MS (method 10): R_(t)=1.10 min; MS (ESIneg): m/z=169 [M−H]⁻

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.72), 0.008(0.71), 4.805 (13.54), 5.046 (1.01), 5.419 (1.07), 7.844 (0.86), 7.863(1.32), 7.904 (0.71), 7.925 (2.18), 7.943 (0.95), 7.971 (1.27), 7.978(1.21), 7.988 (0.78), 7.993 (1.86), 8.006 (0.61), 8.048 (1.80), 8.070(14.52), 8.074 (16.00), 8.095 (2.68).

Intermediate 2664-[5-amino-1-(cyclopropylmethyl)-1H-pyrazol-3-yl]benzonitrile

A solution of 4-(cyanoacetyl)benzonitrile (4.24 g, 24.9 mmol) and(cyclopropylmethyl)hydrazine dihydrochloride (5.94 g, 37.4 mmol) in2-propanol (45 ml) was refluxed overnight. After cooling to ambienttemperature the volume of the mixture was reduced by half under reducedpressure; then diethyl ether was added and the occurring precipitate wascollected filtration, washed with diethyl ether and dried to yield 4.07g (64%) of the desired product.

LC-MS (method 11): R_(t)=1.04 min; MS (ESIpos): m/z=239 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.493 (11.98), 0.510(16.00), 1.303 (0.52), 1.318 (1.19), 1.335 (1.47), 1.350 (1.14), 1.367(0.53), 2.507 (5.85), 4.071 (3.81), 4.088 (2.39), 6.187 (1.83), 7.214(0.55), 7.918 (5.85), 7.939 (7.51), 8.032 (0.44), 8.063 (4.28), 8.075(2.66), 8.082 (2.60).

Intermediate 2674-[5-amino-4-chloro-1-(cyclopropylmethyl)-1H-pyrazol-3-yl]benzonitrile

A solution of4-[5-amino-1-(cyclopropylmethyl)-1H-pyrazol-3-yl]benzonitrile (4.07 g,17.1 mmol) in acetonitrile (50 ml, 950 mmol) was treated with1-chloropyrrolidine-2,5-dione (2.74 g, 20.5 mmol) and dtirred overnightat ambient temperature. The mixture was diluted with water and extractedwith ethyl acetate (3×). The combined organic phases were washed withwater and brine, dried over sodium sulfate and concentrated underreduced pressure. The remaining residue was suspended in diethyl ether,the occurring perecipitate was washed with diethyl ether and dried toyield 1.78 g of the desired product. The filtrate was concentrated underreduced pressure and ourified by flash-chromatography on silica gel(solvent: dichloromethane/ethyl acetate 10:1) to yield 1.90 g. In total3.68 g of the desired product (76%) were obtained.

LC-MS (method 10): R_(t)=1.78 min; MS (ESIpos): m/z=273 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.371 (0.46), 0.383(0.51), 0.480 (0.41), 2.073 (4.07), 2.419 (0.60), 2.565 (16.00), 3.169(12.34), 3.656 (0.48), 3.880 (0.74), 3.897 (0.72), 7.862 (0.62), 7.883(0.84), 7.987 (0.85), 8.008 (0.61).

Intermediate 2681-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methoxy-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylicacid

A solution of ethyl1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methoxy-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(350 mg, 692 μmol) in tetrahydrofuran (4.6 ml, 57 mmol) was treated withaqueous lithium hydroxide solution (3.5 ml, 1.0 M, 3.5 mmol) and stirredovernight at ambient temperature and an additional night at refluxtemperature. After cooling to room temperature the mixture was dilutedwith water and acidified with hydrochloric acid. The mixture wasextracted with ethyl acetate (3×). The combined organic phases weredried over sodium sulfate and concentrated under reduced pressure. Theremaining residue was suspended in acetonitrile, the occurringprecipitate was collected by filtration, washed with acetonitrile anddried to yield 326 mg (82%) of the desired product.

LC-MS (method 9): R_(t)=1.02 min; MS (ESIpos): m/z=478 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.296 (0.87), 0.308(3.43), 0.321 (3.71), 0.333 (1.08), 0.431 (1.08), 0.442 (2.80), 0.444(2.81), 0.461 (2.97), 0.476 (0.76), 1.180 (0.42), 1.192 (0.75), 1.199(0.75), 1.211 (1.05), 1.222 (0.72), 1.229 (0.76), 2.325 (0.87), 2.359(8.59), 2.813 (5.74), 2.911 (16.00), 3.511 (1.55), 3.641 (0.79), 3.777(2.79), 3.793 (2.71), 6.572 (1.46), 6.758 (0.54), 6.779 (0.56), 7.153(0.51), 7.245 (2.31), 7.267 (4.55), 7.289 (2.49), 7.882 (2.16), 7.896(2.73), 7.903 (2.69), 7.918 (2.11), 8.315 (1.57), 8.544 (1.12), 9.841(1.06).

Intermediate 269N′-acetyl-1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methoxy-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbohydrazide

A solution of1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methoxy-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylicacid (331 mg, 83% purity, 575 μmol) and acetohydrazide (128 mg, 1.73mmol) in dimethylformamide (3.0 ml, 39 mmol) was treated with HATU (328mg, 863 μmol) and N,N-diisopropylethylamine (300 μl, 1.7 mmol) andstirred overnight at ambient temperature. The mixture was diluted withwater and extracted with ethyl acetate (3×). The combined organic phaseswere washed with water and brine, dried over sodium sulfate andconcentrated under reduced pressure. The remaining residue was suspendedin dichloromethane, the occurring precipitate was collected byfiltration, washed with dichloromethane and dried to yield 255 mg (83%)of the desired product.

LC-MS (method 10): R_(t)=1.57 min; MS (ESIpos): m/z=534 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.85), 0.008(0.92), 0.291 (0.85), 0.302 (3.71), 0.306 (3.30), 0.317 (3.98), 0.328(1.30), 0.433 (1.13), 0.443 (2.96), 0.447 (2.96), 0.452 (1.70), 0.463(3.22), 0.467 (2.95), 0.479 (0.93), 1.170 (0.40), 1.183 (0.77), 1.189(0.76), 1.201 (1.21), 1.213 (0.72), 1.220 (0.76), 1.233 (0.43), 1.879(1.16), 1.904 (15.07), 2.286 (3.56), 2.690 (1.38), 2.776 (16.00), 2.891(0.43), 3.316 (8.23), 3.568 (2.81), 3.774 (2.64), 3.791 (2.62), 5.754(2.51), 7.246 (2.89), 7.268 (5.85), 7.290 (3.07), 7.883 (2.44), 7.898(2.93), 7.905 (2.86), 7.919 (2.35), 8.542 (1.28), 9.562 (0.55), 9.732(0.94), 9.895 (1.87).

Intermediate 2704-(3-{[6-(4-formyl-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-4-methoxy-1-methyl-1H-pyrazol-5-yl)benzonitrile

A microwave vial was charged1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbaldehyde (291mg, 76% purity, 936 μmol) and4-(3-amino-4-methoxy-1-methyl-1H-pyrazol-5-yl)benzonitrile (235 mg, 1.03mmol) and the contents were suspended in 1,4-dioxane (3.4 ml, 40 mmol).The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (25.7 mg, 28.1 μmol) and Xantphos(32.5 mg, 56.2 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (120 mg, 1.03 mmol) was added. The vial was sealed and heatedat 85° C. for 120 minutes while vigorously stirring. The mixture wasleft at ambient temperature overnight, the reaction mixture was purifiedby preparative HPLC (method: column: Reprosil C18; 10 μm; 125×40mm/flow: 75 mL/min/solvent: A=water (0.1% formic acid),B=acetonitrile/gradient: 0.00-5.50 min=10% B, 17.65-19.48 min=95% B,19.66 min=10% B) to yield the desired product (73 mg, 18%).

LC-MS (method 10): R_(t)=1.67 min; MS (ESIpos): m/z=429 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (0.62), 2.074(0.96), 2.409 (11.88), 2.930 (13.78), 3.540 (0.78), 3.567 (16.00), 3.579(0.42), 3.769 (0.72), 3.786 (13.57), 7.287 (3.14), 7.776 (3.54), 7.780(1.48), 7.793 (3.98), 8.007 (4.16), 8.011 (1.51), 8.020 (1.59), 8.024(3.47), 8.549 (2.48), 9.665 (0.71), 10.014 (5.80).

Intermediate 2711-[6-({1-(cyclopropylmethyl)-3-[4-(difluoromethyl)phenyl]-4-methyl-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3,5-dimethyl-1H-pyrazole-4-carbaldehyde

A microwave vial was charged1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbaldehyde (408mg, 76% purity, 1.31 mmol) and1-(cyclopropylmethyl)-3-[4-(difluoromethyl)phenyl]-4-methyl-1H-pyrazol-5-amine(400 mg, 1.44 mmol) and the contents were suspended in 1,4-dioxane (5.0ml, 58 mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (36.0 mg, 39.3 μmol) and Xantphos(45.5 mg, 78.7 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (167 mg, 1.44 mmol) was added.

The vial was sealed and heated at 85° C. for 90 minutes while vigorouslystirring. The mixture was left overnight at ambient temperature, thereaction mixture was filtered and purified by preparative HPLC (method:column: Reprosil C18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent: A=water(0.01% formic acid), B=acetonitrile/gradient: 0.00-5.00 min=10% B, 6.50min=20% B, 17.0-19.75 min=100% B, 19.75-23.00 min=90% B) and furtherflash-chromatography (column: SNAP KP-Sil 10 g, solvent: 92%dichloromethane/8% ethyl acetate to 66% ethyl acetate) to yield thedesired product (175 mg, 28%).

LC-MS (method 10): R_(t)=2.08 min; MS (ESIpos): m/z=478 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.25-0.35 (m, 2H),0.38-0.54 (m, 2H), 1.13-1.29 (m, 1H), 2.00-2.11 (m, 3H), 2.52-2.57 (m,3H), 2.86-2.99 (m, 3H), 3.80-3.91 (m, 2H), 6.88-7.48 (m, 2H), 7.53-7.69(m, 2H), 7.79-7.95 (m, 2H), 8.41-8.72 (m, 1H), 9.40-9.75 (m, 1H),9.92-10.05 (m, 1H).

Intermediate 272 3-(5-fluoropyridin-2-yl)-4-methyl-1H-pyrazol-5-amine

A solution of 3-(5-fluoropyridin-2-yl)-2-methyl-3-oxopropanenitrile (225mg, 1.26 mmol) in ethanol (2.7 ml) was treated with hydrazine hydrate(1:1) (120 μl, 2.5 mmol) and stirred overnight at 95° C. After coolingto room temperature the mixture was purifified by preparative HPLC(method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent:A=water (0.01% formic acid), B=acetonitrile/gradient: 0.00-5.00 min=10%B, 6.50 min=20% B, 17.0-19.75 min=100% B, 19.75-23.00 min=90% B) toyield 37.8 mg (13%) of the desired product.

LC-MS (method 9): R_(t)=0.45 min; MS (ESIpos): m/z=193 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.113 (16.00), 7.741(1.12), 7.747 (1.19), 7.762 (2.21), 7.768 (1.48), 7.776 (1.48), 7.786(0.49), 8.134 (1.75), 8.557 (1.88), 8.564 (1.91).

Intermediate 2732-[3-(5-fluoropyridin-2-yl)-4-methyl-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione

A solution of 3-(5-fluoropyridin-2-yl)-4-methyl-1H-pyrazol-5-amine (1.75g, 9.11 mmol) and 2-benzofuran-1,3-dione (2.02 g, 13.7 mmol) in aceticacid (25 ml, 440 mmol) was stirred overnight at 140° C. After cooling toambient temperature the mixture was diluted with water. The occurringprecipitate was collected by filtration, washed with water and dried toyield 3.15 g (96%) of the desired product.

Intermediate 2742-[5-(5-fluoropyridin-2-yl)-1,4-dimethyl-1H-pyrazol-3-yl]-1H-isoindole-1,3(2H)-dione

A solution of2-[3-(5-fluoropyridin-2-yl)-4-methyl-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(3.10 g, 9.62 mmol) in dimethylformamide (30 ml, 390 mmol) was treatedwith cesium carbonate (6.27 g, 19.2 mmol) and iodomethane (1.2 ml, 19mmol). The mixture was stirred overnight. The mixture was filtered andpurged into saturated ammonium chloride solution. The occurringprecipitate was collected by filtration washed with water and dried. Thecrude product was purified using flash-chromatography (column: SNAPUltra 50 g, solvent: 96% dichloromethane/4% ethyl acetate to 34% ethylacetate) and further preparative HPLC (method: column: Reprosil C18; 10μm; 125×30 mm/flow: 50 mL/min/solvent: A=water (0.01% formic acid),B=acetonitrile/gradient: 0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75min=100% B, 19.75-23.00 min=90% B) to yield 580 mg of the desiredproduct (18%) along with its regioisomer.

LC-MS (method 10): R_(t)=1.64 min; MS (ESIpos): m/z=337 [M+H]⁺

¹H-NMR (600 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.940 (15.51), 3.939(16.00), 7.783 (1.11), 7.790 (1.16), 7.797 (1.38), 7.804 (1.33), 7.923(0.83), 7.928 (0.89), 7.938 (1.54), 7.943 (1.72), 7.948 (2.58), 7.953(3.12), 7.957 (3.28), 7.962 (3.69), 7.968 (0.52), 8.005 (0.48), 8.011(3.78), 8.016 (2.65), 8.020 (2.69), 8.025 (2.43), 8.800 (2.29), 8.805(2.26).

Intermediate 2752-[3-(5-fluoropyridin-2-yl)-1,4-dimethyl-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione

A solution of2-[3-(5-fluoropyridin-2-yl)-4-methyl-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(3.10 g, 9.62 mmol) in N,N-dimethylformamide (30 ml, 390 mmol) wastreated with cesium carbonate (6.27 g, 19.2 mmol) and iodomethane (1.2ml, 19 mmol). The mixture was stirred overnight. The mixture wasfiltered and purged into saturated ammonium chloride solution. Theoccurring precipitate was collected by filtration washed with water anddried. The crude product was purified using flash-chromatography(column: SNAP Ultra 50 g, solvent: 96% dichloromethane/4% ethyl acetateto 34% ethyl acetate) and further preparative HPLC (method: column:Reprosil C18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent: A=water (0.01%formic acid), B=acetonitrile/gradient: 0.00-5.00 min=10% B, 6.50 min=20%B, 17.0-19.75 min=100% B, 19.75-23.00 min=90% B) to yield 212 mg of thedesired product (6%) along with its regioisomer.

LC-MS (method 10): R_(t)=1.82 min; MS (ESIpos): m/z=337 [M+H]⁺

¹H-NMR (600 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.178 (16.00), 3.321(5.42), 5.753 (0.59), 7.778 (0.61), 7.783 (0.65), 7.793 (1.29), 7.798(1.35), 7.807 (0.71), 7.812 (0.73), 7.976 (2.33), 7.980 (2.50), 7.984(2.67), 7.990 (4.16), 7.998 (1.68), 8.006 (1.23), 8.013 (1.18), 8.043(0.46), 8.049 (3.38), 8.055 (2.65), 8.059 (2.52), 8.064 (2.32), 8.611(2.36), 8.616 (2.35).

Intermediate 2765-(5-fluoropyridin-2-yl)-1,4-dimethyl-1H-pyrazol-3-amine

A solution of2-[5-(5-fluoropyridin-2-yl)-1,4-dimethyl-1H-pyrazol-3-yl]-1H-isoindole-1,3(2H)-dione(206 mg, 612 μmol) in ethanol (7 mL) was treated with hydrazinemonohydrate (137 μL, 2.8 mmol) and stirred at 90° C. overnight. Aftercooling to ambient temperature the mixture was diluted with water andextracted with ethyl acetate (3×). The combined organic phases werewashed with saturated sodium hydrogen carbonate solution and brine,dried over sodium sulfate and concentrated under reduced pressure toyield 108 mg (86%) of the desired product.

LC-MS (method 9): R_(t)=0.47 min; MS (ESIpos): m/z=207 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.870 (16.00), 3.315(6.20), 3.587 (0.43), 4.494 (3.22), 7.557 (1.20), 7.566 (1.20), 7.574(1.36), 7.583 (1.29), 7.826 (0.87), 7.832 (0.91), 7.844 (1.62), 7.850(1.65), 7.861 (0.77), 7.867 (0.78), 8.699 (2.25), 8.705 (2.17).

Intermediate 2773-(5-fluoropyridin-2-yl)-1,4-dimethyl-1H-pyrazol-5-amine

A solution of2-[3-(5-fluoropyridin-2-yl)-1,4-dimethyl-1H-pyrazol-5-yl]-1H-isoindole-1,3(2H)-dione(747 mg, 2.22 mmol) in ethanol (20 mL) was treated with hydrazinemonohydrate (540 μl, 11.1 mmol) and stirred at 90° C. overnight. Aftercooling to ambient temperature the mixture was diluted with water andextracted with ethyl acetate (3×). The combined organic phases werewashed with saturated sodium hydrogen carbonate solution and brine,dried over sodium sulfate and concentrated under reduced pressure toyield 322 mg (67%) of the desired product.

LC-MS (method 9): R_(t)=0.49 min; MS (ESIpos): m/z=207 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.748 (0.57), 2.139(15.49), 3.590 (16.00), 4.978 (4.23), 7.634 (0.65), 7.640 (0.67), 7.652(1.39), 7.658 (1.40), 7.670 (0.78), 7.676 (0.76), 7.840 (1.31), 7.849(1.32), 7.857 (1.12), 7.867 (1.04), 8.499 (2.25), 8.505 (2.12).

Intermediate 2784-{5-[(6-chloropyrimidin-4-yl)amino]-1,4-dimethyl-1H-pyrazol-3-yl}benzonitrile

A solution of 4,6-dichloropyrimidine (140 mg, 942 μmol) and4-(5-amino-1,4-dimethyl-1H-pyrazol-3-yl)benzonitrile (200 mg, 942 μmol)in dimethylformamide (4.4 ml, 57 mmol) was treated withN,N-diisopropylethylamine (180 μl, 1.0 mmol) and sodium iodide (169 mg,1.13 mmol). The resulting mixture was stirred three days at 125° C.After cooling to ambient temperature the mixture was purified bypreparative HPLC (method: column: Reprosil C18; 10 μm; 125×40 mm/flow:75 mL/min/solvent: A=water (0.1% formic acid), B=acetonitrile/gradient:0.00-5.50 min=10% B, 17.65-19.48 min=95% B, 19.66 min=10% B) to yield74.0 mg (24%) of the desired product.

LC-MS (method 9): R_(t)=0.83 min; MS (ESIpos): m/z=325 [M+H]⁺

Intermediate 2794-{5-[(6-hydrazinylpyrimidin-4-yl)amino]-1,4-dimethyl-1H-pyrazol-3-yl}benzonitrile

A solution of4-{5-[(6-chloropyrimidin-4-yl)amino]-1,4-dimethyl-1H-pyrazol-3-yl}benzonitrile(73.0 mg, 225 μmol) and hydrazine hydrate (1:1) (33 μl, 670 μmol) in1,4-dioxane (1.4 ml) was stirred overnight at 70° C. As there was nocomplete conversion observed, in total further 19 equivalents ofhydrazine hydrate (208 μL, 4.27 mmol) was added in portions during oneweek. Stirring at 80° C. was continued. After cooling to roomtemperature the mixture was concentrated under reduced pressure to yield92.0 mg (64%) as the crude product which was used in the next stepwithout further purifications.

LC-MS (method 11): R_(t)=0.71 min; MS (ESIpos): m/z=321 [M+H]⁺

Intermediate 280 2-methyl-3-(6-methylpyridin-3-yl)-3-oxopropanenitrile

To a solution of methyl 6-methylpyridine-3-carboxylate (3.43 g, 22.7mmol) and propanenitrile (2.1 ml, 29 mmol) in tetrahydrofuran (48 ml,590 mmol) cooled in an ice bath was added lithium bistrimethylsilylamide1M in tetrahydrofuran (29 ml, 1.0 M, 29 mmol) dropwise and the reactionmixture stirred at room temperature overnight. The reaction mixture wascooled in an ice bath and additional propanenitrile (0.81 ml, 11 mmol)was added followed by the dropwise addition of Lithiumbistrimethylsilylamide 1M in tetrahydrofuran (11.3 ml, 1.0 M, 11.3 mmol)and the reaction then stirred at room temperature for a further 3 h. Thereaction was quenched with ice cold water, and the organic phase solventthen removed in vacuo. The residue was diluted with water (110 ml),acidified to pH 4-5 with 4N hydrochloric acid amd extracted three timeswwith methyl tert-butyl ether. The combined organic phase s were driedwith sodium sulfate and concentrated in vacuo. The crude product waspurified by flash-chromatography on silica gel (dichloromethane:methanol60:1, column: Biotage SNAP Ultra 50 g) and the residue washed withpentane to yield 3.15 g (100% purity, 80% yield) of the desired product.The target compounds is an approximate 1:1 mixture with its tautomer insolution as determineded by NMR.

LC-MS (Method 10): R_(t)=0.94 min; MS (ESIpos): m/z=175 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.008 (0.41), 1.025(0.41), 1.106 (2.24), 1.188 (0.42), 1.470 (8.27), 1.488 (8.34), 1.680(2.51), 1.869 (16.00), 2.520 (15.02), 2.576 (14.43), 3.077 (0.73), 5.108(0.67), 5.126 (2.07), 5.144 (2.05), 5.162 (0.65), 7.351 (2.11), 7.371(2.30), 7.477 (2.06), 7.497 (2.17), 7.812 (1.62), 7.817 (1.65), 7.832(1.49), 7.838 (1.52), 8.232 (1.53), 8.238 (1.55), 8.253 (1.46), 8.259(1.46), 8.591 (2.43), 8.596 (2.40), 9.048 (2.36), 9.053 (2.32), 10.997(1.22).

Intermediate 2811-(cyclopropylmethyl)-4-methyl-3-(6-methylpyridin-3-yl)-1H-pyrazol-5-amine

To rac-2-methyl-3-(6-methylpyridin-3-yl)-3-oxopropanenitrile (500 mg,2.87 mmol) in 2-propanol (7.5 ml, 97 mmol) at an internal temperature of80° C. was slowly added (cyclopropylmethyl)hydrazine dihydrochloride(502 mg, 3.16 mmol) and the reaction heated at reflux overnight. Thecooled reaction was concentrated in vacuo, the residue dissolved inwater and solid sodium hydrogen carbonate added until the solution waspH 7. The aqueous solution was extracted three times with ethyl acetateand the combined organic phase s dried with sodium sulfate andconcentrated in vacuo. The crude product was purified byflash-chromatography on silica gel (dichloromethane:methanol 40:1,column: Biotage SNAP Ultra 10 g) to yield 555 mg (100% purity, 80%yield) of the desired product.

LC-MS (Method 10): R_(t)=0.69 min; MS (ESIpos): m/z=243 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.335 (0.53), 0.348(2.52), 0.360 (2.95), 0.372 (0.95), 0.414 (0.95), 0.423 (2.21), 0.433(1.37), 0.443 (2.41), 0.459 (0.51), 1.187 (0.68), 1.206 (0.89), 1.217(0.59), 1.982 (16.00), 2.466 (12.89), 3.801 (4.40), 3.818 (4.34), 4.951(5.35), 5.754 (0.46), 7.233 (2.01), 7.253 (2.15), 7.802 (1.68), 7.807(1.53), 7.822 (1.57), 7.827 (1.43), 8.632 (2.85), 8.636 (2.67).

Intermediate 2823-(4-fluorophenyl)-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-amine

To rac-3-(4-fluorophenyl)-2-methyl-3-oxopropanenitrile (4.38 g, 24 7mmol) in 2-propanol (64 ml, 840 mmol) at an internal temperature of 80°C. was slowly added (2-methoxyethyl)hydrazine ethanedioate (1:1) (4.90g, 27.2 mmol) and the reaction heated at reflux for 3.5 h. The cooledreaction mixture was filtered and concentrated in vacuo. The residue wasdissolved in ethylacteate, basified with a saturated aqueous solution ofsodium bicarbonate to pH 7 and extracted three times with ethyl acetate.The combined organic phase s were dried with sodium sulfate andconcentrated in vacuo. The crude product was purified byflash-chromatography on silica gel (gradient 15% to 100% ethylacetate incyclohexane, column: Biotage SNAP Ultra 100 g) to yield 2.34 g (100%purity, 38% yield) of the desired product.

LC-MS (Method 10): R_(t)=1.26 min; MS (ESIpos): m/z=250 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.236 (1.58), 1.973(13.74), 3.252 (16.00), 3.508 (1.01), 3.613 (2.09), 3.625 (4.42), 3.637(2.24), 4.052 (2.20), 4.064 (4.13), 4.075 (1.95), 4.889 (4.34), 7.172(1.83), 7.190 (3.67), 7.208 (1.97), 7.581 (2.03), 7.592 (2.42), 7.598(2.28), 7.609 (1.86).

Intermediate 283 methyl 4-[(tert-butoxycarbonyl)(methyl)amino]benzoate

To methyl 4-(methylamino)benzoate (3.99 g, 24.1 mmol) in tetrahydrofuran(48 ml, 590 mmol) was added di-tert-butyl dicarbonate (5.8 ml, 25 mmol)and N,N-dimethylpyridin-4-amine (295 mg, 2.41 mmol) and the reactionstirred overnight at room temperature. The reaction mixture was thendiluted with ethylacetate, washed twice with water, once with a saturedaqueous solution of sodium chloride, the organic phase then dried withsodium sulfate and concentrated in vacuo. The crude product was purifiedby flash-chromatography on silica gel (gradient of ethylacetate incyclohexane, column: Biotage SNAP Ultra 50 g) to yield 2.79 g (100%purity, 44% yield) of the desired product.

LC-MS (Method 9): R_(t)=1.05 min; MS (ESIpos): m/z=266 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.420 (16.00), 3.310(2.45), 3.840 (5.81), 7.440 (1.41), 7.462 (1.53), 7.905 (1.63), 7.909(0.53), 7.922 (0.51), 7.927 (1.44).

Intermediate 284 rac-tert-butyl[4-(2-cyanopropanoyl)phenyl]methylcarbamate

To a solution of methyl 4-[(tert-butoxycarbonyl)(methyl)amino]benzoate(2.68 g, 10.1 mmol) and propanenitrile (1.4 ml, 20 mmol) intetrahydrofuran (21 ml, 260 mmol) cooled in an ice bath was addedlithium bistrimethylsilylamide 1M in tetrahydrofuran (21 ml, 1.0 M, 21mmol) dropwise and the reaction mixture stirred at room temperature for1 h. The reaction was quenched with ice cold water, and the organicphase solvent then removed in vacuo. The residue was diluted with water,extracted three times with dichloromethane. The combined organic phase swere dried with sodium sulfate and concentrated in vacuo to yield aportion the target compound (1.015 g, 80% purity). The aqueous phase wassubsequently acidified with 4N hydrochloric acid to pH 4 and extractedthree times with dichloromethane and once with methyl tert-butylether.The combined organic phase s were dried with sodium sulfate andconcentrated in vacuo to yield 2.31 g (100% purity, 79% yield) of thedesired product. The target compounds is an approximate 2:1 mixture withits tautomer in solution as determineded by NMR.

LC-MS (Method 9): R_(t)=1.00 min; MS (ESIneg): m/z=287 [M−H]⁻

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.416 (4.56), 1.436(16.00), 1.464 (2.96), 1.482 (2.95), 1.856 (1.42), 3.217 (1.60), 3.262(6.12), 5.101 (0.71), 5.119 (0.70), 7.396 (0.49), 7.506 (0.68), 7.513(1.56), 7.535 (1.62), 7.980 (1.59), 8.001 (1.45).

Intermediate 2851-(cyclopropylmethyl)-4-methyl-3-[4-(methylamino)phenyl]-1H-pyrazol-5-amine

To tert-butyl [4-(2-cyanopropanoyl)phenyl]methylcarbamate (476 mg, 1.65mmol) in 2-propanol (4.3 ml, 56 mmol) at an internal temperature of 80°C. was slowly added (cyclopropylmethyl)hydrazine dihydrochloride (289mg, 1.82 mmol) and the reaction heated at reflux for 3.5 h. The cooledreaction mixture was filtered and concentrated in vacuo. The residue wasdissolved in ethylacteate, diluted with water, basified with a saturatedaqueous solution of sodium hydrogen carbonate until pH 7 and extractedthree times with ethyl acetate. The combined organic phase s were driedwith sodium sulfate and concentrated in vacuo. The crude product waspurified by flash-chromatography on silica gel (dichloromethane:methanol60:1, column: Biotage SNAP Ultra 25 g) to yield 259 mg (100% purity, 61%yield) of the desired product.

LC-MS (Method 10): R_(t)=1.00 min; MS (ESIpos): m/z=257 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.321 (0.65), 0.330(2.34), 0.333 (2.23), 0.340 (2.56), 0.350 (0.88), 0.400 (0.99), 0.407(2.10), 0.411 (1.78), 0.416 (1.22), 0.423 (2.20), 0.426 (1.68), 0.436(0.56), 1.166 (0.54), 1.172 (0.57), 1.174 (0.61), 1.181 (0.82), 1.188(0.52), 1.191 (0.50), 1.195 (0.48), 1.934 (16.00), 2.674 (6.36), 2.684(6.17), 3.164 (0.62), 3.175 (0.62), 3.747 (3.97), 3.760 (3.86), 4.746(4.99), 5.581 (0.98), 5.591 (0.97), 5.751 (1.08), 6.520 (3.97), 6.537(4.01), 7.303 (4.27), 7.320 (3.87).

Intermediate 286 tert-butyl2-(6-chloropyrimidin-4-yl)-2,6-dihydropyrrolo[3,4-c]pyrazole-5(4H)-carboxylate

To 4,6-dichloropyrimidine (674 mg, 4.52 mmol) in dimethylformamide (3.4ml) under an atmosphere of argon was added tert-butyl2,6-dihydropyrrolo[3,4-c]pyrazole-5(4H)-carboxylate (946 mg, 4.52 mmol)and cesium carbonate (1.47 g, 4.52 mmol) and the reaction stirredovernight at room temperature. The reaction was poured onto water (25ml) and stirred for 60 minutes. The precipitate was filtered andpurified by HPLC (Method 20) to yield 748 mg (100% purity, 51% yield) ofthe desired product.

LC-MS (Method 10): R_(t)=2.10 min; MS (ESIpos): m/z=322 [M+H]⁺

¹H-NMR (600 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.466 (16.00), 4.400(1.20), 4.427 (1.38), 4.456 (1.47), 4.477 (1.29), 7.884 (0.67), 7.903(0.79), 8.467 (0.69), 8.493 (0.62), 8.925 (1.44).

Intermediate 287 ethyl 4-(difluoromethoxy)benzoate

To ethanol (53 ml) at −10° C. was added thionyl chloride (1.03 ml, 14.1mmol) dropwise, maintaining the temperature under 0° C. at all times.After stirring for 10 minutes at 0° C. 4-(difluoromethoxy)benzoic acid(500 mg, 2.66 mmol) was added and the reaction was stirred overnight atreflux. The cooled reaction mixture was diluted with water and theethanol removed in vacuo. The aqueous phase was basified with 2N sodiumhydroxide to pH 7, extracted three times with dichloromethane and thecombined organic phase s then washed with a satured aqueous solution ofsodium chloride, dried with sodium sulfate and concentrated in vacuo toyield 578 mg, (100% purity, 100% yield) of the desired product.

LC-MS (Method 9): R_(t)=0.99 min; Compound does not ionise.

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.302 (7.48), 1.320(16.00), 1.337 (7.72), 4.287 (2.40), 4.305 (7.40), 4.322 (7.35), 4.340(2.32), 7.210 (2.52), 7.288 (5.54), 7.310 (5.90), 7.393 (5.04), 7.577(2.45), 8.000 (0.86), 8.007 (7.30), 8.012 (2.32), 8.024 (2.26), 8.029(6.84), 8.036 (0.78).

Intermediate 2883-[4-(difluoromethoxy)phenyl]-2-methyl-3-oxopropanenitrile

To a solution of ethyl 4-(difluoromethoxy)benzoate (578 mg, 2.67 mmol)and propanenitrile (250 μl, 3.5 mmol) in tetrahydrofuran (5.6 ml, 69mmol) cooled in an ice bath was added lithium bistrimethylsilylamide 1Min tetrahydrofuran (3.5 ml, 1.0 M, 3.5 mmol) dropwise and the reactionmixture stirred at room temperature overnight. The reaction was quenchedwith ice cold water, and the organic phase solvent then removed invacuo. The residue was diluted with water (24 ml), acidified to pH 4with 4N hydrochloric acid amd extracted three times wwith methyltert-butyl ether. The combined organic phase s dried with sodium sulfateand concentrated in vacuo to yield 406 mg (88% purity, 59% yield) of thedesired product. The target compounds is an approximate 4.5:1 mixturewith its tautomer in solution as determineded by NMR.

LC-MS (Method 10): R_(t)=1.61 min; MS (ESIpos): m/z=226 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.106 (1.02), 1.463(15.91), 1.481 (16.00), 1.673 (2.08), 1.857 (11.95), 2.328 (0.41), 2.366(0.44), 2.669 (0.44), 2.710 (0.41), 5.103 (1.23), 5.121 (3.95), 5.139(3.95), 5.157 (1.22), 7.157 (1.08), 7.193 (0.53), 7.257 (3.02), 7.269(3.41), 7.278 (3.70), 7.341 (2.47), 7.353 (6.79), 7.375 (7.35), 7.452(5.60), 7.473 (0.62), 7.495 (0.44), 7.525 (1.09), 7.561 (0.53), 7.597(3.53), 7.619 (3.18), 7.635 (2.83), 7.985 (1.45), 8.007 (1.46), 8.091(8.30), 8.113 (7.76), 10.863 (1.27).

Intermediate 2891-(cyclopropylmethyl)-3-[4-(difluoromethoxy)phenyl]-4-methyl-1H-pyrazol-5-amine

To 3-[4-(difluoromethoxy)phenyl]-2-methyl-3-oxopropanenitrile (406 mg,1.80 mmol) in 2-propanol (4.7 ml, 61 mmol) at an internal temperature of80° C. was slowly added (cyclopropylmethyl)hydrazine dihydrochloride(315 mg, 1.98 mmol) and the reaction heated at reflux overnight. Thecooled reaction was concentrated in vacuo, the residue dissolved inwater (5 ml) and the solution basified to pH 7 with solid sodiumhydrogen carbonate. The aqueous solution was extracted three times withethyl acetate and the combined organic phase s dried with sodium sulfateand concentrated in vacuo. The crude product was purified byflash-chromatography on silica gel (gradient of ethylacetate incyclohexane, column: Biotage SNAP Ultra 10 g) to yield 403 mg (95%purity, 76% yield) of the desired product.

LC-MS (Method 10): R_(t)=1.52 min; MS (ESIpos): m/z=294 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.331 (0.53), 0.343(2.05), 0.347 (2.06), 0.356 (2.44), 0.369 (0.93), 0.412 (0.96), 0.421(1.89), 0.425 (1.58), 0.432 (1.22), 0.441 (2.08), 0.457 (0.53), 1.182(0.50), 1.190 (0.48), 1.202 (0.77), 1.214 (0.46), 1.219 (0.44), 1.982(16.00), 3.791 (3.95), 3.808 (3.88), 4.911 (4.52), 7.042 (1.40), 7.162(3.43), 7.184 (3.79), 7.228 (2.80), 7.414 (1.36), 7.598 (0.57), 7.605(4.50), 7.610 (1.48), 7.622 (1.46), 7.627 (4.04), 7.634 (0.47).

Intermediate 290 ethyl 6-oxo-1,6-dihydropyridine-3-carboxylate

To ethanol (150 ml) at −10° C. was added thionyl chloride (1.9 ml, 26mmol) dropwise, maintaining the temperature under 0° C. at all times.After stirring for 10 minutes 6-methoxypyridine-3-carboxylic acid (2.00g, 13.1 mmol) was added and the reaction was stirred overnight atreflux. The cooled reaction mixture was diluted with water and theethanol removed in vacuo. The aqueous phase was basified with 1N sodiumhydroxide to pH 7, extracted three times with dichloromethane and thecombined organic phase s then washed with a saturated aqueous solutionof sodium chloride, dried with sodium sulfate and concentrated in vacuoto yield 1.87 g, (100% purity, 86% yield) of the desired product.

LC-MS (method 10): R_(t)=0.8 min; Compound does not ionise.

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.255 (7.51), 1.270(16.00), 1.284 (7.57), 4.206 (2.38), 4.220 (7.44), 4.234 (7.34), 4.249(2.26), 6.357 (3.35), 6.376 (3.44), 7.777 (2.77), 7.783 (2.82), 7.797(2.67), 7.802 (2.76), 8.017 (3.23), 8.023 (3.12), 12.112 (0.67).

Intermediate 291 ethyl 6-methoxypyridine-3-carboxylate

To ethyl 6-oxo-1,6-dihydropyridine-3-carboxylate (1.87 g, 11.2 mmol) inchloroform (25 ml) was added iodomethane (2.5 ml, 40 mmol) and silvercarbonate (4.02 g, 14.6 mmol) and the reaction stirred overnight at roomtemperature. The cooled reaction mixture was filtered, concentrated invacuo and purified by flash-chromatography on silica gel (gradient 7% to60% ethylacetate in cyclohexane, column: Biotage SNAP Ultra 50 g) toyield 1.05 g (100% purity, 51% yield) of the desired product.

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.304 (3.72), 1.318(7.82), 1.333 (3.74), 1.993 (0.47), 3.938 (16.00), 4.290 (1.20), 4.305(3.68), 4.319 (3.62), 4.333 (1.14), 6.922 (1.68), 6.939 (1.73), 6.941(1.68), 8.150 (1.43), 8.155 (1.44), 8.168 (1.39), 8.172 (1.39), 8.748(1.48), 8.752 (1.48).

Intermediate 292rac-3-(6-methoxypyridin-3-yl)-2-methyl-3-oxopropanenitrile

To a solution of ethyl 6-methoxypyridine-3-carboxylate (1.02 g, 5.61mmol) and propanenitrile (520 μl, 7.3 mmol) in tetrahydrofuran (12 ml,150 mmol) cooled in an ice bath was added lithium bistrimethylsilylamide1M in tetrahydrofuran (7.3 ml, 1.0 M, 7.3 mmol) dropwise and thereaction mixture stirred at room temperature for 3 h. The reactionmixture was cooled in an ice bath and additional lithiumbistrimethylsilylamide 1M in tetrahydrofuran (2.8 ml, 1.0 M, 2.8 mmol)was added dropwise and the reaction stirred overnight at roomtemperature. The reaction mixture was cooled in an ice bath andadditional lithium bistrimethylsilylamide 1M in tetrahydrofuran (1.12ml, 1.0 M, 1.2 mmol) was added dropwise and the reaction stirred for 2 hat room temperature. The reaction was quenched with ice cold water, andthe organic phase solvent then removed in vacuo. The residue was dilutedwith water, acidified to pH 4 with 4N hydrochloric acid amd extractedthree times with dichloromethane. The combined organic phase s driedwith sodium sulfate, concentrated in vacuo and purified byflash-chromatography on silica gel (gradient 7% to 65% ethylacetate incyclohexane, column: Biotage SNAP Ultra 50 g) to yield 729 mg (99%purity, 67% yield) of the desired product. The target compounds is anapproximate 2.5:1 mixture with its tautomer in solution, as determinedby NMR.

LC-MS (method 9): R_(t)=0.69 min; MS (ESIpos): m/z=191 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.470 (7.51), 1.484(7.48), 1.694 (0.88), 1.821 (0.26), 1.854 (3.10), 3.895 (1.69), 3.900(3.33), 3.925 (0.36), 3.969 (16.00), 5.067 (0.63), 5.082 (1.90), 5.096(1.88), 5.110 (0.59), 6.905 (0.60), 6.922 (0.63), 6.992 (2.26), 7.009(2.29), 7.736 (0.09), 7.741 (0.09), 7.753 (0.08), 7.758 (0.09), 7.841(0.37), 7.854 (0.36), 8.229 (1.52), 8.234 (1.62), 8.246 (1.47), 8.251(1.45), 8.362 (0.66), 8.897 (2.36), 8.902 (2.30), 10.901 (0.06).

Intermediate 2931-(cyclopropylmethyl)-3-(6-methoxypyridin-3-yl)-4-methyl-1H-pyrazol-5-amine

To 3-(6-methoxypyridin-3-yl)-2-methyl-3-oxopropanenitrile (372 mg, 1.95mmol) in 2-propanol (5.2 ml, 67 mmol) at an internal temperature of 80°C. was slowly added (cyclopropylmethyl)hydrazine dihydrochloride (342mg, 2.15 mmol) and the reaction heated at reflux overnight. The cooledreaction was concentrated in vacuo, the residue dissolved inethylacetate, basified with 1 N sodium hydroxide and extracted twicewith ethylacetate. The combined organic phase s were dried with sodiumsulfate and concentrated in vacuo. The resultant material was thenstirred in ethylacetate, filtered and the organic phase concentrated invacuo. The crude product was purified by flash-chromatography on silicagel (dichloromethane:methanol 50:1, column: Biotage SNAP Ultra 25 g) toyield 111 mg (100% purity, 22% yield) of the desired product.

LC-MS (method 9): R_(t)=0.63 min; MS (ESIpos): m/z=259 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.336 (0.41), 0.345(1.43), 0.349 (1.35), 0.355 (1.54), 0.358 (1.38), 0.366 (0.62), 0.416(0.67), 0.423 (1.32), 0.427 (1.12), 0.432 (0.79), 0.436 (0.72), 0.439(1.40), 0.443 (1.04), 0.452 (0.41), 1.199 (0.55), 1.968 (12.62), 3.790(2.76), 3.804 (2.70), 3.865 (16.00), 4.927 (3.02), 6.820 (1.71), 6.821(1.62), 6.837 (1.73), 6.838 (1.65), 7.868 (1.46), 7.873 (1.45), 7.886(1.35), 7.890 (1.38), 8.323 (1.61), 8.325 (1.62), 8.328 (1.62), 8.329(1.45).

Intermediate 2943-(6-methoxypyridin-3-yl)-1,4-dimethyl-1H-pyrazol-5-amine

To 3-(6-methoxypyridin-3-yl)-2-methyl-3-oxopropanenitrile (356 mg, 1.87mmol) in 2-propanol (5.0 ml, 64 mmol) at an internal temperature of 80°C. was slowly added methylhydrazine (110 μl, 2.1 mmol) and the reactionheated at reflux overnight. The cooled reaction was concentrated invacuo, the residue dissolved in ethylacetate, basified with 1 N sodiumhydroxide and extracted twice with ethylacetate. The combined organicphase s were dried with sodium sulfate, concentrated in vacuo and thecrude product was purified by flash-chromatography on silica gel(dichloromethane:methanol 40:1, column: Biotage SNAP Ultra 50 g) toyield 294 mg (91% purity, 65% yield) of the desired product.

LC-MS (method 10): R_(t)=0.90 min; MS (ESIpos): m/z=219 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.758 (1.51), 1.963(13.54), 3.446 (1.56), 3.556 (13.94), 3.861 (16.00), 3.903 (1.88), 4.974(3.14), 6.816 (1.71), 6.817 (1.68), 6.833 (1.75), 6.834 (1.71), 7.853(1.44), 7.858 (1.44), 7.870 (1.35), 7.875 (1.37), 8.313 (1.61), 8.315(1.66), 8.318 (1.63), 8.319 (1.51).

Intermediate 295 ethyl 6-(difluoromethyl)pyridine-3-carboxylate

Under an argon atmosphere, 6-(difluoromethyl)pyridine-3-carboxylic acid(1.43 g, 8.24 mmol) was dissolved in thionylchloride (15 mL, 210 mmol)and the reaction mixture was refluxed for 30 minutes. After cooling toambient temperature, the contents of the flask were concentratedin-vacuo. The residue was dissolved in dry ethanol (50 mL) and thereaction mixture refluxed for 1 h. The mixture was then concentrated anddried to yield the desired product as a dark oil (1.65 g, 98% yield),that was used in the next step without further purification.

LC-MS (method 10): R_(t)=1.52 min; MS (ESIpos): m/z=202 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.167 (0.55), 1.225(1.66), 1.240 (3.37), 1.254 (1.67), 1.332 (7.55), 1.346 (16.00), 1.360(7.50), 1.981 (1.01), 3.993 (0.67), 4.003 (0.71), 4.007 (0.68), 4.018(0.68), 4.357 (2.38), 4.371 (7.31), 4.385 (7.14), 4.399 (2.23), 6.947(1.85), 7.056 (3.75), 7.165 (1.71), 7.849 (2.68), 7.865 (2.80), 8.467(1.85), 8.471 (1.79), 8.484 (1.73), 8.488 (1.66), 9.156 (2.74), 9.159(2.65).

Intermediate 2963-[6-(difluoromethyl)pyridin-3-yl]-2-methyl-3-oxopropanenitrile

Under an argon atmosphere, ethyl6-(difluoromethyl)pyridine-3-carboxylate (2.07 g, 10.3 mmol) andpropanenitrile (1.1 ml, 15 mmol) were dissolved in dry tetrahydrofuran(16 mL) and chilled with a water bath. A solution of lithiumbis(trimethylsilyl)amide in tetrahydrofuran (16 mL, 1.0 M, 16 mmol) wasadded dropwise. The reaction mixture was then allowed to stir overnightat ambient temperature. It was diluted with water and extracted withethyl acetate. The organic phase was discarded and the aqueous phaseacidified with aqueous hydrochloric acid solution (1 M) to pH 5. It wasthen extracted with ethyl acetate (3×). The combined organic phaseextracts were washed with brine, dried over sodium sulfate andconcentrated to yield the desired product (1.8 g, 79% yield), that wasused in the next step without further purification

LC-MS (method 11): R_(t)=0.90 min; MS (ESIpos): m/z=211 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.496 (0.74), 1.510(0.74), 1.689 (2.38), 1.906 (12.19), 1.910 (16.00), 1.989 (0.24), 2.267(0.17), 5.192 (0.20), 5.207 (0.19), 6.920 (0.97), 6.945 (0.20), 7.030(1.94), 7.054 (0.40), 7.080 (0.22), 7.139 (0.92), 7.163 (0.18), 7.811(1.75), 7.828 (1.91), 7.849 (0.30), 7.920 (0.24), 7.935 (0.24), 8.054(0.20), 8.058 (0.19), 8.070 (0.18), 8.074 (0.17), 8.156 (1.28), 8.160(1.26), 8.172 (1.16), 8.176 (1.11), 8.451 (0.18), 8.455 (0.18), 8.467(0.17), 8.471 (0.16), 8.545 (0.22), 8.561 (0.20), 8.735 (0.30), 8.738(0.29), 8.841 (2.12), 9.148 (0.25), 9.152 (0.24), 9.248 (0.34).

Intermediate 2973-[6-(difluoromethyl)pyridin-3-yl]-1,4-dimethyl-1H-pyrazol-5-amine

3-[6-(difluoromethyl)pyridin-3-yl]-2-methyl-3-oxopropanenitrile (650 mg,3.09 mmol) and methylhydrazine (180 μl, 3.4 mmol) were dissolved in2-propanol (20 mL) and the reaction mixture was refluxed for 4 h. Aftercooling to ambient temperature, water (20 mL) and saturated aqueoussodium hydrogencarbonate solution was added until pH 8 was obtained. Thesuspension was then extracted with ethyl acetate (3×), the combinedorganic phase extracts were washed with brine, dried over sodium sulfateand concentrated. The residue was dissolved in acetonitrile/water andlyophilized to yield the desired product as an off-white powder (591 mg,76% yield).

LC-MS (method 11): R_(t)=0.80 min; MS (ESIpos): m/z=239 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.811 (0.63), 2.025(0.24), 2.038 (15.79), 3.509 (0.65), 3.606 (16.00), 5.098 (3.57), 6.848(1.06), 6.958 (2.18), 7.068 (0.92), 7.688 (1.56), 7.704 (1.68), 8.120(1.07), 8.125 (1.05), 8.137 (0.97), 8.141 (0.95), 8.883 (1.57), 8.886(1.56).

Intermediate 298 tert-butyl[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl][6-(3,5-dimethyl-4-nitro-1H-pyrazol-1-yl)pyrimidin-4-yl]carbamate

N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-dimethyl-4-nitro-1H-pyrazol-1-yl)pyrimidin-4-amine(310 mg, 670 μmol) and (293 mg, 1.34 mmol) were dissolved indichloromethane (13 mL) and 4-dimethylaminopyridine (8.19 mg, 67.0 μmol)was added. The reaction mixture was stirred overnight at ambienttemperature. It was quenched by addition of aqueous satured ammoniumchloride solution and extracted with dichloromethane (3×). The combinedorganic phase extracts were washed with brine, dried over sodium sulfateand concentrated to yield the desired product (300 mg, 76% yield)

LC-MS (method 11): R_(t)=1.76 min; MS (ESIpos): m/z=463 [M-BOC+H]⁺

¹H NMR (500 MHz, dimethylsulfoxide-d₆) δ ppm: 0.19-0.32 (m, 2H),0.38-0.52 (m, 2H), 1.13-1.21 (m, 1H), 1.46 (s, 9H), 1.99 (s, 3H), 2.56(s, 3H), 3.03 (s, 3H), 3.66-3.75 (m, 1H), 3.75-3.86 (m, 1H), 7.22-7.33(m, 2H), 7.69-7.80 (m, 2H), 8.59-8.70 (m, 1H), 8.81-8.91 (m, 1H).

Intermediate 299 tert-butyl[6-(4-amino-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl][1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]carbamate

Under an argon atmosphere, tert-butyl[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl][6-(3,5-dimethyl-4-nitro-1H-pyrazol-1-yl)pyrimidin-4-yl]carbamate(126 mg, 224 μmol) was dissolved in tetrahydrofuran (2 mL) and ethanol(1.5 mL) and palladium(II)hydroxide on charcoal (20%, 45 mg, 64.1 μmol)was added. The argon atmosphere was replaced by a hydrogen atmosphere (1bar) and the reaction mixture was stirred overnight. After removing thehydrogen atmosphere, the reaction mixture was filtered over celite andthe filtrate was concentrated to yield the desired product (118 mg, 69%yield, 71% purity), that was used in the next step without furtherpurification.

LC-MS (method 11): Rt=1.57 min; MS (ESIpos): m/z=433 [M-BOC+H]⁺

Intermediate 300 ethyl1-(6-{[4-(difluoromethoxy)-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

Under an argon atmosphere4-(difluoromethoxy)-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (250mg, 972 μmol), ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (300mg, 1.07 mmol) and sodium phenolate (124 mg, 1.07 mmol) and the contentswere suspended in 1,4-dioxane (5.0 mL). The reaction mixture wasdegassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (26.7mg, 29.2 μmol) and XantPhos (33.7 mg, 58.3 μmol) were added and thereaction mixture was degassed again for 1 min. The vial was sealed andheated at 85° C. overnight while vigorously shaking. After cooling toambient temperature, the reaction mixture was diluted with ethylacetate, filtered over Celite and concentrated. The residue was purifiedby flash column chromatography (SNAP 25 g, cyclohexane/ethyl acetategradient 90/10 to 20/80) and further by preparative HPLC (Reprosil C18,10 μM, 250×50 mm, 150 mL/min, acetonitrile/water (containing 0.1% TFA)gradient 5/95 to 95/5) to yield the desired product (119 mg, 23% yield).

LC-MS (method 10): R_(t)=2.23 min; MS (ESIpos): m/z=502 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.019 (0.86), 1.230(2.96), 1.298 (5.05), 1.312 (9.21), 1.326 (4.79), 2.394 (15.45), 2.902(16.00), 3.734 (15.80), 4.239 (1.76), 4.253 (4.51), 4.267 (4.43), 4.281(1.65), 6.657 (1.32), 6.805 (2.58), 6.952 (1.25), 7.388 (4.80), 7.406(5.31), 7.423 (2.98), 7.595 (3.08), 7.606 (3.92), 7.622 (2.66), 8.546(4.39), 9.707 (3.05).

Intermediate 301 tert-butyl[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]{6-[4-(ethylamino)-3,5-dimethyl-1H-pyrazol-1-yl]pyrimidin-4-yl}carbamate

Under an argon atmosphere, tert-butyl[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl][6-(3,5-dimethyl-4-nitro-1H-pyrazol-1-yl)pyrimidin-4-yl]carbamate(300 mg, 70% purity, 373 μmol) was dissolved in ethanol (6.0 mL) andpalladium on charcoal (10%, 37.5 mg) was added. The argon atmosphere wasreplaced by a hydrogen atmosphere (1 bar) and the reaction mixture wasstirred overnight for 30 h. The reaction mixture was then filtered overCelite and the filtrate was concentrated. The residue was purified byflash column chromatography (SNAP Ultra 10 g, cyclohexane/ethyl acetategradient 95/5 to 35/65) to yield the desired product (25.0 mg, 11%yield) along with tert-butyl[6-(4-amino-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl][1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]carbamate(see above, 24 mg, 12% yield) as a by-product.

LC-MS (method 11): R_(t)=1.66 min; MS (ESIpos): m/z=460 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (0.97), 0.007(0.66), 0.212 (0.19), 0.220 (0.33), 0.230 (0.41), 0.238 (0.38), 0.248(0.21), 0.261 (0.22), 0.271 (0.40), 0.279 (0.45), 0.289 (0.34), 0.298(0.22), 0.401 (0.32), 0.409 (0.33), 0.418 (0.35), 0.425 (0.24), 0.428(0.24), 0.435 (0.20), 0.447 (0.21), 0.455 (0.23), 0.458 (0.21), 0.465(0.33), 0.473 (0.31), 0.482 (0.30), 1.034 (1.86), 1.048 (4.06), 1.062(1.89), 1.137 (0.23), 1.142 (0.23), 1.151 (0.34), 1.161 (0.23), 1.165(0.22), 1.235 (0.18), 1.398 (0.17), 1.424 (0.79), 1.441 (16.00), 1.553(0.17), 1.978 (6.16), 2.167 (0.32), 2.212 (6.01), 2.557 (0.19), 2.571(5.98), 2.858 (0.21), 2.872 (0.77), 2.886 (1.11), 2.900 (0.76), 2.914(0.21), 3.651 (0.34), 3.665 (0.34), 3.680 (0.52), 3.694 (0.51), 3.725(0.28), 3.739 (0.52), 3.752 (0.28), 3.764 (0.53), 3.778 (0.51), 3.793(0.34), 3.806 (0.31), 5.753 (5.53), 7.252 (0.94), 7.257 (0.35), 7.266(0.51), 7.270 (1.83), 7.274 (0.43), 7.284 (0.40), 7.288 (0.96), 7.717(0.95), 7.722 (0.46), 7.728 (1.05), 7.735 (0.99), 7.742 (0.41), 7.746(0.83), 8.468 (1.80), 8.470 (1.81), 8.623 (1.81), 8.625 (1.73).

Intermediate 302[1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]methanol

Under an argon atmosphere,1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbaldehyde (1.00g, 4.23 mmol) was dissolved in tetrahydrofuran and acetic acid (480 μl,8.5 mmol) was added. Sodium triacetoxyborohydride (1.41 g, 95% purity,6.34 mmol) was then added and the reaction mixture was stirred atambient temperature overnight. Another batch of sodiumtriacetoxyborohydride (0.94 g, 95% purity, 4.23 mmol) and acetic acid(480 μl, 8.5 mmol) was added and the reaction mixture was stirred foranother 6 h. The reaction mixture was then carefully quenched withaqueous saturated ammonium chloride solution and extracted with ethylacetate (2×). The combined organic phase extracts were dried over sodiumsulfate and concentrated. The residue was purified by flash columnchromatography (SNAP Ultra 25g, cyclohexane/ethyl acetate gradient) toyield the desired product (740 mg, 66% yield).

LC-MS (method 11): Rt=0.95 min; MS (ESIpos): m/z=239 [M+H]+

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.254 (16.00), 2.446(0.74), 2.650 (15.10), 2.971 (0.72), 4.316 (4.64), 4.326 (4.74), 4.802(1.52), 4.812 (3.22), 4.823 (1.35), 7.886 (3.92), 7.888 (3.74), 8.891(3.53), 8.893 (3.36).

Intermediate 3034-chloro-6-[4-(methoxymethyl)-3,5-dimethyl-1H-pyrazol-1-yl]pyrimidine

Under an argon atmosphere,[1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]methanol (660mg, 90% purity, 2.49 mmol) was dissolved in acetonitrile (20 mL) andsilver(I) oxide (1.15 g, 4.98 mmol) and methyl iodide (770 μl, 12 mmol)were added. The reaction mixture was stirred at 60° C. overnight.Another batch of silver(I) oxide (0.58 g, 2.49 mmol) and methyl iodide(154 μL, 12 mmol) were added and the reaction mixture stirred overnightat 60° C. Water and saturated aqueous ammonium chloride solution wasadded and the resulting suspension filtered. The filtrate was extractedwith ethyl acetate (2×). The combined organic phase extracts were driedover sodium sulfate and concentrated. The residue was purified bypreparative HPLC (column: Reprosil C18; 250*50 mm, 10 μM, flow 150mL/min, gradient acetonitrile/water (containing 0.1% trifluoroaceticacid) 10/90 to 90/10) to yield the desired product (60 mg, 8% yield)

LC-MS (method 10): Rt=1.84 min; MS (ESIpos): m/z=253 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (0.65), 0.007(0.44), 2.240 (12.46), 2.274 (2.37), 2.664 (11.63), 2.697 (2.24), 3.234(16.00), 3.692 (3.15), 4.280 (7.19), 5.060 (1.33), 7.907 (2.99), 7.909(2.89), 7.920 (0.61), 7.921 (0.59), 8.909 (2.66), 8.911 (2.56), 8.930(0.55), 8.932 (0.53).

Intermediate 304 1-benzyl-3,5-dimethyl-1H-pyrazole

3,5-dimethyl-1H-pyrazole (10.0 g, 104 mmol) was dissolved inacetonitrile (250 mL) and potassium carbonate (17.3 g, 125 mmol) wasadded. (bromomethyl)benzene (15 ml, 120 mmol) was then added and thereaction mixture stirred overnight at ambient temperature. Theprecipitated solid was filtered off and the filtrate was concentrated.The residue was purified by flash column chromatography (SNAP Ultra 100g, cyclohexane/ethyl acetate gradient 88/12 to 0/100) to yield thedesired product (13.0 g, 66% yield).

LC-MS (method 11): R_(t)=1.15 min; MS (ESIpos): m/z=187 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.092 (16.00), 2.143(14.03), 5.177 (8.08), 5.841 (2.78), 7.070 (2.30), 7.088 (2.73), 7.249(1.35), 7.267 (1.14), 7.300 (2.40), 7.315 (1.71), 7.319 (3.17), 7.332(0.49), 7.336 (1.16).

Intermediate 3051-(1-benzyl-3,5-dimethyl-1H-pyrazol-4-yl)-2,2,2-trifluoroethanone

Under an argon atmosphere, 1-benzyl-3,5-dimethyl-1H-pyrazole (7.46 g,40.0 mmol) was dissolved in pyridine (19 mL) and the resulting solutionwas cooled to 0° C. trifluoroacetic anhydride (6.2 mL, 44 mmol) wasadded dropwise via syringe and the reaction mixture was allowed to warmto ambient temperature while stirring overnight. Another aliquot oftrifluoroacetic anhydride (2.0 mL, 14.2 mmol) was added and the reactionmixture was stirred another 3 h at ambient temperature. Water was addedand the mixture was extracted with ethyl acetate (2×). The combinedorganic phase extracts were dried over sodium sulfate and concentrated.The residue was purified by flash column chromatography (SNAP Ultra 100g, cyclohexane/ethyl acetate gradient 95/5 to 20/80) to yield thedesired product (7.84 g, 65% yield).

LC-MS (method 11): R_(t)=1.40 min; MS (ESIpos): m/z=283 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (2.06), 0.006(1.26), 2.338 (10.68), 2.340 (9.98), 2.488 (16.00), 5.382 (9.11), 7.185(3.00), 7.200 (3.81), 7.203 (2.72), 7.289 (0.65), 7.292 (0.42), 7.299(0.58), 7.304 (2.03), 7.308 (0.61), 7.316 (1.13), 7.319 (1.70), 7.321(0.85), 7.348 (3.43), 7.350 (1.47), 7.360 (2.52), 7.363 (4.33), 7.366(0.95), 7.373 (0.72), 7.377 (1.67), 7.379 (0.91).

Intermediate 306(±)-1-(1-benzyl-3,5-dimethyl-1H-pyrazol-4-yl)-2,2,2-trifluoroethanol(racemate)

1-(1-benzyl-3,5-dimethyl-1H-pyrazol-4-yl)-2,2,2-trifluoroethanone (4.37g, 15.5 mmol) was dissolved in MeOH (31 mL) and sodium borohydride (193mg, 5.10 mmol) was added at ambient temperature while stirring. Thereaction mixture was quenched with saturated aqueous ammonium chloridesolution and extracted with ethyl acetate (3×). The combined organicphase extracts were washed with brine, dried over sodium sulfate andconcentrated to yield the desired product (4.27 g, 97% yield), which wasused in the next step without further purification.

LC-MS (method 11): R_(t)=1.13 min; MS (ESIpos): m/z=285 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (0.82), 0.006(0.57), 1.987 (0.54), 2.138 (15.71), 2.193 (16.00), 4.987 (0.89), 4.997(0.96), 5.003 (0.85), 5.013 (0.82), 5.208 (7.68), 6.442 (4.03), 6.452(4.00), 6.509 (0.42), 7.093 (2.80), 7.107 (3.29), 7.109 (2.47), 7.245(0.60), 7.255 (0.50), 7.260 (1.83), 7.264 (0.54), 7.275 (1.36), 7.314(2.87), 7.316 (1.19), 7.329 (4.05), 7.340 (0.67), 7.343 (1.58).

Intermediate 3071-benzyl-4-[(±)-1-chloro-2,2,2-trifluoroethyl]-3,5-dimethyl-1H-pyrazole(racemate)

Under an argon atmosphere, a microwave vial was charged with(±)-1-(1-benzyl-3,5-dimethyl-1H-pyrazol-4-yl)-2,2,2-trifluoroethanol(racemate, 500 mg, 1.76 mmol) and 1,2-dichloroethane (4.0 mL) was added.Thionylchloride (320 μl, 4.4 mmol) was then added and the vial wassealed. It was heated to 60° C. overnight while vigorously shaking.After cooling to ambient temperature, the mixture was concentrated andthe residue redissolved in dichloromethane and washed with water. Theorganic phase layer was dried over sodium sulfate and concentrated. Thedesired product thus obtained (380 mg, 64% yield) was used in the nextstep without further purification.

LC-MS (method 11): R_(t)=1.41 min; MS (ESIpos): m/z=303 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.209 (13.27), 2.263(16.00), 5.243 (7.85), 6.034 (0.64), 6.050 (1.80), 6.066 (1.65), 6.082(0.49), 7.099 (2.86), 7.113 (3.32), 7.261 (0.59), 7.271 (0.51), 7.275(1.80), 7.290 (1.36), 7.327 (2.83), 7.342 (3.99), 7.354 (0.69), 7.357(1.54).

Intermediate 308(±)-1-(1-benzyl-3,5-dimethyl-1H-pyrazol-4-yl)-2,2,2-trifluoro-N,N-dimethylethanamine(racemate)

1-benzyl-4-[(1R)-1-chloro-2,2,2-trifluoroethyl]-3,5-dimethyl-1H-pyrazole(380 mg, 1.26 mmol) was dissolved in acetonitrile (7 mL) and an aqueoussolution of N-methylmethanamine (40%, 320 μL) was added. The reactionmixture was heated overnight at 60° C. After cooling to ambienttemperature, a second aliquot of an aqueous solution ofN-methylmethanamine (40%, 250 μL) was added. The reaction mixture washeated at 60° C. for another 6.5 h. After cooling to ambienttemperature, the reaction mixture was concentrated. The residue waspurified by flash column chromatography (SNAP Ultra 10 g,cyclohexane/ethyl acetate gradient 90/10 to 20/80) to yield the desiredproduct (100 mg, 25% yield).

LC-MS (method 11): R_(t)=1.26 min; MS (ESIpos): m/z=312 [M+H]⁺

Intermediate 309(±)-1-(3,5-dimethyl-1H-pyrazol-4-yl)-2,2,2-trifluoro-N,N-dimethylethanamine(racemate)

Under an argon atmosphere,(±)-1-(1-benzyl-3,5-dimethyl-1H-pyrazol-4-yl)-2,2,2-trifluoro-N,N-dimethylethanamine(105 mg, 337 μmol) was dissolved in tetrahydrofuran (1.9 mL) and aqueousHCl solution (230 μL). Palladium(II)hydroxide on charcoal (20%, 79.3 mg,113 μmol) was then added and the argon atmosphere replaced by anhydrogen atmosphere (1 bar). The reaction mixture was stirred overnightat ambient temperature. The reaction mixture was filtered throughcelite, rinsed with ethyl acetate and the filtrate was diluted withethyl acetate. It was washed with aqueous sodium hydrogencarbonatesolution and the aqueous phase extracted with ethyl acetate. Thecombined organic phase layers were dried over sodium sulfate andconcentrated to yield the desired product (35 mg, 47% yield) that wasused in the next step without further purification.

LC-MS (method 11): R_(t)=0.58 min; MS (ESIpos): m/z=222 [M+H]⁺

Intermediate 310(±)-1-[1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]-2,2,2-trifluoro-N,N-dimethylethanamine(racemate)

Under an argon atmosphere,(±)-1-(3,5-dimethyl-1H-pyrazol-4-yl)-2,2,2-trifluoro-N,N-dimethylethanamine(35.0 mg, 158 μmol) was dissolved in N,N-dimethylformamide and4,6-dichloropyrimidine (25.9 mg, 174 μmol) and potassium carbonate (23.0mg, 166 μmol) was added. The reaction mixture was stirred at ambienttemperature overnight. A second batch of potassium carbonate (16.4 mg,119 μmol) was added and the reaction mixture was stirred overnight atambient temperature.

The remaining solids were removed by filtration and the filtratepurified by preparative HPLC (column: Chromatorex C18; 125*30 mm, 10 μM,flow 75 mL/min, gradient acetonitrile/water (containing 0.1%trifluoroacetic acid) 10/90 to 90/10) to yield the desired product (8.0mg, 13% yield).

LC-MS (method 11): R_(t)=1.55 min; MS (ESIpos): m/z=289 [M-NMe₂]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.294 (16.00), 2.742(9.77), 4.154 (0.20), 4.172 (0.55), 4.189 (0.51), 4.206 (0.18), 5.752(0.80), 7.950 (3.31), 7.952 (3.21), 8.943 (2.97), 8.945 (2.87).

Intermediate 311{[1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]oxy}acetonitrile

Under an argon atmosphere,1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-ol (300 mg, 1.34mmol) was dissolved in dimethylformamide (6.0 mL) and potassiumcarbonate (221 mg, 1.60 mmol) and bromoacetonitrile (120 μl, 1.7 mmol)were added. The reaction mixture was stirred at ambient temperature for3 h. The reaction mixture was then poured onto water (30 mL) andextracted with dichloromethane (2×). The combined organic phase extractswere washed with brine, dried over magnesium sulfate and concentrated toyield the desired product (180 mg, 49% yield) that was used in the nextstep without further purification.

LC-MS (method 11): Rt=1.23 min; MS (ESIpos): m/z=264 [M+H]⁺

¹H-NMR (500 MHz, DIMETHYLSULFOXIDE-d6) δ [ppm]: 2.126 (0.86), 2.274(16.00), 2.343 (0.88), 2.521 (0.96), 2.524 (1.17), 2.628 (15.87), 4.993(12.60), 7.903 (3.92), 7.905 (3.81), 8.911 (3.72), 8.913 (3.55).

Intermediate 3124-chloro-6-(4-iodo-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine

Under an argon atmosphere,4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (1.00 g, 4.79 mmol)was dissolved in acetonitrile and the resulting solution heated to 50°C. 1-iodopyrrolidine-2,5-dione (1.29 g, 5.75 mmol) was added in twoportions and the reaction mixture stirred at 40° C. overnight. Thereaction mixture was stirred another 2.5 h at 55° C. and cooled toambient temperature. Water was added and the mixture extracted withethyl acetate (2×). The combined organic extracts were dried over sodiumsulfate and concentrated. The residue was purified by flash columnchromatography (SNAP Ultra 25 g, cyclohexane/ethyl acetate gradient) toyield the desired product (1.21 g, 71% yield).

LC-MS (method 11): Rt=1.57 min; MS (ESIpos): m/z=335 [M+H]⁺

¹H-NMR (500 MHz, DIMETHYLSULFOXIDE-d6) δ [ppm]: 2.224 (0.80), 2.246(15.83), 2.657 (0.49), 2.658 (0.47), 2.711 (16.00), 7.917 (3.82), 7.919(3.69), 8.937 (3.41), 8.938 (3.28).

Intermediate 313 ethyl[1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl](difluoro)acetate

Under an argon atmosphere, copper powder (794 mg, 12 5 mmol) wasactivated by stirring 10 min in each of the following: aqueous hydrogenchloride solution (1 m), water, methanol, acetone and then dried underhigh vacuum. A solution of ethyl bromo(difluoro)acetate (400 μl, 3.1mmol) in dimethylsulfoxide (10 mL) was added and the reaction mixturestirred for 1 h at ambient temperature.4-chloro-6-(4-iodo-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (1.10 g, 95%purity, 3.12 mmol) was then added and the reaction mixture stirredovernight at ambient temperature. The reaction mixture was then heatedto 50° C. for 3 h, when additional aliquots of activated copper (250 mg,3.94 mmol) and ethyl bromo(difluoro)acetate (400 μl, 3.1 mmol) wereadded. The reaction mixture was stirred another 4 h at 50° C. andovernight at ambient temperature. It was then quenched by addition ofsaturated aqueous ammonium chloride solution and extracted with ethylacetate (3×). The combined organic extracts were washed with brine,dried over sodium sulfate and concentrated. The residue was purified byflash column chromatography (SNAP Ultra 100 g, cyclohexane/ethyl acetategradient) to yield an impure product (108 mg, 54% purity, 6% yield) thatwas used in the next step without further purification.

LC-MS (method 11): Rt=1.51 min; MS (ESIpos): m/z=331 [M+H]⁺

Intermediate 314 ethyl[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl](difluoro)acetate

A microwave vial was charged with1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine(88.1 mg, 359 μmol) and ethyl[1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl](difluoro)acetate(108 mg, 327 μmol) and the contents were suspended in dioxane (0.84 mL).The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (8.97 mg, 9.80 μmol) and XantPhos(11.3 mg, 19.6 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was heated at 85° C. and sodium phenolate(41.7 mg, 359 μmol) was added, the vial was sealed and heated for 180min while vigorously shaking. After cooling to ambient temperature, thereaction mixture was quenched by addition of aqueous hydrogen chloridesolution and extracted with ethyl acetate (3×). The combined organicextracts were washed with brine, dried over sodium sulfate andconcentrated. The residue was purified by preparative HPLC (column:Chromatorex C18; 125*30 mm, 10 μM, flow 75 mL/min, gradientacetonitrile/water (containing 0.1% trifluoroacetic acid) 10/90 to 95/5)to yield the desired product (33 mg, 75% purity, 13% yield).

LC-MS (method 11): Rt=1.61 min; MS (ESIpos): m/z=540 [M+H]⁺

¹H-NMR (600 MHz, DIMETHYLSULFOXIDE-d6) δ [ppm]: 0.005 (0.39), 0.294(2.46), 0.428 (2.96), 0.441 (2.91), 1.096 (0.19), 1.158 (0.22), 1.172(0.58), 1.180 (1.03), 1.184 (0.97), 1.192 (1.52), 1.200 (0.96), 1.204(1.05), 1.212 (0.68), 1.237 (3.55), 1.242 (7.21), 1.249 (6.29), 1.254(12.76), 1.260 (3.31), 1.265 (6.08), 1.346 (0.45), 1.358 (0.28), 1.913(0.20), 2.007 (16.00), 2.163 (0.32), 2.202 (0.81), 2.285 (9.48), 2.388(0.40), 2.477 (0.35), 2.616 (0.38), 2.637 (0.35), 2.706 (10.11), 2.727(9.33), 2.816 (0.17), 3.835 (1.77), 4.314 (3.02), 4.326 (6.32), 4.338(5.48), 4.350 (1.78), 4.413 (0.19), 4.425 (0.17), 7.264 (2.48), 7.269(3.95), 7.279 (5.50), 7.282 (5.61), 7.294 (7.23), 7.328 (1.05), 7.340(2.16), 7.352 (1.34), 7.493 (2.55), 7.507 (3.46), 7.520 (2.09), 7.729(1.95), 8.502 (0.26), 8.758 (4.33), 9.512 (0.23).

Intermediate 3154-chloro-6-[4-(cyclopropylmethoxy)-3,5-dimethyl-1H-pyrazol-1-yl]pyrimidine

Under an argon atmosphere,1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-ol (300 mg, 1.34mmol), potassium carbonate (221 mg, 1.60 mmol) and(bromomethyl)cyclopropane (270 mg, 2.00 mmol) were suspended inN,N-dimethylformamide (5.0 mL). The reaction mixture was stirred atambient temperature for 24 h. It was poured onto water (30 mL) andextracted with ethyl acetate (3×). The combined organic extracts werewashed with brine, dried over magnesium sulfate and concentrated. Theresidue was suspended in acetonitrile and the remaining solid wasfiltered off. The filtrate was purified by preparative HPLC (column:Chromatorex C18; 125*30 mm, 10 μM, flow 75 mL/min, gradientacetonitrile/water (containing 0.1% trifluoroacetic acid) 10/90 to 95/5)to yield the desired product (46 mg, 12% yield).

LC-MS (method 11): R_(t)=1.51 min; MS (ESIpos): m/z=279 [M+H]⁺

Intermediate 3164-chloro-6-[4-(difluoromethoxy)-3,5-dimethyl-1H-pyrazol-1-yl]pyrimidine

Under an argon atmosphere, potassium hydroxide (1.50 g, 26.7 mmol) wasdissolved in water (6.5 mL) and acetonitrile (6.5 mL) was added and themixture was stirred. When this mixture became homogeneous, it was cooledto −78° C. The dry ice bath was replaced by an ice bath and the mixtureallowed to slowly warm to 0° C. As soon as stirring was possible again,1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-ol (300 mg, 1.34mmol) was added. diethyl [bromo(difluoro)methyl]phosphonate (240 μl, 1.3mmol) was then added drop-wise over 5 min. After 30 min, a secondaliquot of diethyl [bromo(difluoro)methyl]phosphonate (240 μl, 1.3 mmol)and the reaction mixture stirred for another 30 min for a total of 1 h.The reaction mixture was then neutralized by addition of aqueoushydrogen chloride solution (2 N) and extracted with methyl tert-butylether (3×). The combined organic extracts were washed with brine, driedover sodium sulfate and concentrated. The desired product thus obtained(485 mg, 75% purity, 99% yield) was used in the next step withoutfurther purification.

LC-MS (method 11): R_(t)=1.40 min; MS (ESIpos): m/z=275 [M+H]⁺

Intermediate 3171-(cyclopropylmethyl)-3-[6-(difluoromethyl)pyridin-3-yl]-4-methyl-1H-pyrazol-5-amine

3-[6-(difluoromethyl)pyridin-3-yl]-2-methyl-3-oxopropanenitrile (650 mg,3.09 mmol) and (cyclopropylmethyl)hydrazine-hydrogen chloride (1/2) (615mg, 3.87 mmol) were dissolved in 2-propanol (20 mL) and the reactionmixture was refluxed for 4 h. After cooling to ambient temperature,water and solid sodium hydrogen carbonate were added (gas evolution)until pH 8 was reached. The resulting suspension was then extracted withethyl acetate (3×), the combined organic extracts were washed withbrine, dried over sodium sulfate and concentrated. The residue wasredissolved in acetonitrile/water and lyophilized to yield the desiredproduct (691 mg, 80% yield).

LC-MS (method 11): R_(t)=1.01 min; MS (ESIpos): m/z=279 [M+H]⁺

¹H-NMR (500 MHz, DIMETHYLSULFOXIDE-d6) δ [ppm]: 0.355 (0.59), 0.364(2.02), 0.367 (1.91), 0.374 (2.19), 0.376 (1.95), 0.384 (0.83), 0.432(0.93), 0.439 (1.86), 0.443 (1.54), 0.448 (1.09), 0.456 (1.94), 0.459(1.45), 0.468 (0.54), 1.210 (0.48), 1.216 (0.46), 1.226 (0.76), 1.236(0.46), 1.240 (0.42), 2.039 (16.00), 3.840 (3.77), 3.854 (3.69), 5.055(4.17), 6.850 (1.15), 6.960 (2.42), 7.070 (1.00), 7.692 (1.82), 7.709(1.95), 8.131 (1.26), 8.135 (1.23), 8.147 (1.13), 8.151 (1.11), 8.887(1.97), 8.891 (1.94).

Intermediate 318 methyl 4-carbamoylcubane-1-carboxylate

Under an argon atmosphere, 4-(methoxycarbonyl)cubane-1-carboxylic acid(800 mg, 3.88 mmol) was dissolved in tetrahydrofuran (10 mL). Thesolution was then cooled to −10° C., at which point a solution oftriethylamine (590 μl, 4.3 mmol) in tetrahydrofuran (3 mL) followed byethyl chloroformate (410 μl, 4.3 mmol) were added dropwise. The reactionmixture was stirred at −10° C. for 10 min, when a solution of ammonia(0.5 M in tetrahydrofuran, 78 mL, 39 mmol) was added dropwise. Thereaction mixture was then stirred at ambient temperature overnight. Itwas quenched by addition of water and diluted with ethyl acetate. Afterphase separation, the organic layer was washed with water (25 ml),aqueous hydrogen chloride solution (2 N), saturated aqueous sodiumhydrogencarbonate solution and brine, dried over sodium sulfate andconcentrated to yield the desired product (325 mg, 39% yield) that wasused in the next step without further purification.

¹H-NMR (500 MHz, DIMETHYLSULFOXIDE-d6) δ [ppm]: 1.139 (0.24), 1.357(1.35), 2.184 (0.18), 3.625 (6.57), 3.628 (1.22), 4.100 (16.00), 4.141(0.23), 4.147 (0.23), 4.177 (0.32), 6.970 (0.27), 7.278 (0.25).

Intermediate 319 methyl 4-cyanocubane-1-carboxylate

Under an argon atmosphere, methyl 4-carbamoylcubane-1-carboxylate (325mg, 1.58 mmol) was dissolved in 1,2-dichloroethane (10 mL) andphosphorous oxychloride (740 μl, 7.9 mmol) was added drop-wise. Thereaction mixture was then refluxed for 30 min. After cooling to ambienttemperature, saturated aqueous sodium hydrogencarbonate solution wasslowly added while stirring. The organic phase was separated and washedwith water and brine, dried over sodium sulfate and concentratedin-vacuo. The residue was purified by flash column chromatography (SNAPUltra 50 g, cyclohexane/ethyl acetate 100:0 to 40:60) to afford thedesired product as a white solid (181 mg, 61% yield).

¹H-NMR (500 MHz, DIMETHYLSULFOXIDE-d6) δ [ppm]: −0.007 (0.87), 1.398(1.53), 3.309 (16.00), 4.236 (3.64), 4.244 (5.20), 4.246 (5.97), 4.251(2.82), 4.255 (5.83), 4.261 (0.62), 4.332 (6.03), 4.337 (2.97), 4.341(5.85), 4.352 (3.44).

Intermediate 320 4-(2-cyanopropanoyl)cubane-1-carbonitrile

Under an argon atmosphere, methyl 4-cyanocubane-1-carboxylate (175 mg,935 μmol) and propanenitrile (100 μL, 1.4 mmol) were dissolved in drytetrahydrofuran (1.5 mL) and the reaction mixture was chilled with awater bath. A solution of LiHMDS (1.4 ml, 1.0 M in tetrahydrofuran, 1.4mmol) was added dropwise and the reaction mixture was stirred at ambienttemperature for 3 h. It was then diluted with water and extracted withethyl acetate. The organic phase was discarded and the aqueous phase wasacidified with aqueous hydrogen chloride solution (1 M) until pH 5 wasobtained and extracted with ethyl acetate (3×). The combined organicextracts were washed with brine, dried over sodium sulfate andconcentrated to yield the desired product (161 mg, 74% yield) that wasused in the next step without further purification.

LC-MS (method 11): R_(t)=0.90 min; MS (ESIneg): m/z=209 [M−H]⁻

¹H-NMR (500 MHz, DIMETHYLSULFOXIDE-d6) δ [ppm]: −0.007 (1.99), 0.006(1.40), 1.236 (1.19), 1.268 (0.51), 1.346 (4.72), 1.377 (2.08), 1.606(0.64), 1.687 (4.60), 2.072 (1.59), 3.621 (1.11), 4.197 (1.64), 4.207(2.13), 4.216 (2.15), 4.246 (0.79), 4.255 (0.70), 4.328 (12.84), 4.386(16.00).

Intermediate 3214-[5-amino-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-3-yl]cubane-1-carbonitrile

4-(2-cyanopropanoyl)cubane-1-carbonitrile (161 mg, 85% purity, 651 μmol)and (cyclopropylmethyl)hydrazine hydrogen chloride (1:2) (129 mg, 814μmol) were dissolved in 2-propanol (5 mL) and the reaction mixture washeated to reflux while vigorously stirring for 4 h. After cooling toambient temperature, water (20 mL) and solid sodium hydrogencarbonatewas added (gas evolution) until pH 8 was reached. The suspension wasthen extracted with ethyl acetate (2×). The combined organic extractswere washed with brine, dried over sodium sulfate and concentrated toyield the desired product (109 mg, 59% yield) that was used in the nextstep without further purification.

LC-MS (method 10): R_(t)=1.05 min; MS (ESIpos): m/z=279 [M+H]⁺

¹H-NMR (500 MHz, DIMETHYLSULFOXIDE-d6) δ [ppm]: −0.120 (0.17), −0.007(2.01), 0.007 (1.15), 0.117 (0.16), 0.275 (0.61), 0.284 (2.09), 0.287(1.88), 0.294 (2.10), 0.296 (1.91), 0.304 (0.81), 0.377 (0.88), 0.385(1.84), 0.389 (1.74), 0.393 (1.03), 0.398 (1.00), 0.401 (1.92), 0.405(1.62), 0.413 (0.59), 1.095 (0.20), 1.099 (0.25), 1.108 (0.46), 1.115(0.46), 1.118 (0.38), 1.124 (0.75), 1.131 (0.38), 1.134 (0.43), 1.138(0.43), 1.148 (0.24), 1.154 (0.22), 1.179 (3.18), 1.192 (3.16), 1.236(0.25), 1.742 (16.00), 1.784 (0.21), 3.659 (3.60), 3.673 (3.57), 4.081(0.28), 4.177 (2.71), 4.180 (1.22), 4.186 (3.14), 4.188 (3.43), 4.197(3.65), 4.202 (0.48), 4.209 (0.49), 4.220 (0.60), 4.229 (0.63), 4.324(0.60), 4.329 (3.87), 4.331 (2.15), 4.338 (3.81), 4.340 (3.62), 4.349(2.78), 4.743 (3.71), 4.886 (0.23), 4.898 (0.28), 4.911 (0.21).

Intermediate 3221-benzyl-3,5-dimethyl-4-[2-(trifluoromethyl)-1,3-dioxolan-2-yl]-1H-pyrazole

Under an argon atmosphere,1-(1-benzyl-3,5-dimethyl-1H-pyrazol-4-yl)-2,2,2-trifluoroethan-1-one(10.0 g, 35.4 mmol) and 2-chloroethan-1-ol (12 ml, 180 mmol) weredissolved in N,N-dimethylformamide (35 mL) and tetrahydrofuran (30 mL)and the resulting solution was cooled to −78° C. A solution of potassium2-methylpropan-2-olate (19.9 g, 177 mmol) in tetrahydrofuran (54 mL) andN,N-dimethylformamide (30 mL) was added dropwise. The cooling bath wasremoved and the reaction mixture allowed to warm to ambient temperature.After 2 h stirring at ambient temperature, it was quenched withsaturated, aqueous ammonium chloride solution and diluted with water. Itwas extracted with ethyl acetate (3×) and the combined organic extractswere washed with brine (3×), dried over sodium sulfate and concentratedto yield the desired product (11.7 g, 96% yield) that was used in thenext step without further purification.

LC-MS (method 10): R_(t)=2.00 min; MS (ESIpos): m/z=327 [M+H]⁺

¹H-NMR (500 MHz, DIMETHYLSULFOXIDE-d6) δ [ppm]: 2.183 (16.00), 2.244(14.97), 2.732 (3.04), 2.887 (3.73), 3.592 (0.60), 3.601 (0.58), 3.603(0.61), 4.017 (0.75), 4.032 (2.61), 4.045 (1.04), 4.159 (1.51), 4.166(1.35), 4.173 (2.82), 4.187 (0.98), 5.225 (7.24), 7.096 (2.60), 7.111(3.00), 7.251 (0.56), 7.261 (0.46), 7.266 (1.69), 7.270 (0.48), 7.278(0.81), 7.280 (1.23), 7.320 (2.62), 7.323 (1.07), 7.335 (3.70), 7.346(0.61), 7.349 (1.43), 7.956 (0.46).

Intermediate 3233,5-dimethyl-4-[2-(trifluoromethyl)-1,3-dioxolan-2-yl]-1H-pyrazole

Under an argon atmosphere,1-benzyl-3,5-dimethyl-4-[2-(trifluoromethyl)-1,3-dioxolan-2-yl]-1H-pyrazole(11.6 g, 35.5 mmol) was dissolved in tetrahydrofuran/water (9:1, 260 mL)and palladium(II)hydroxide on charcoal (20%, 2.50 g, 3.55 mmol) wereadded and the reaction mixture chilled with a water bath. The argonatmosphere was replace by an hydrogen atmosphere and the reactionmixture stirred vigorously overnight. A second aliquot ofpalladium(II)hydroxide on charcoal (20%, 774 mg, 1.10 mmol) was addedand the reaction mixture was further hydrogenated under atmosphericpressure overnight. The reaction mixture was filtered over Celite,washed further with tetrahydrofuran and concentrated. The residue wasdissolved in dichloromethane and evaporated to dryness (5 cycles) toremove residual water to yield the desired product (7.75 g, 90% yield)that was used in the next step without further purification.

LC-MS (method 11): R_(t)=1.00 min; MS (ESIpos): m/z=237 [M+H]⁺

¹H-NMR (500 MHz, DIMETHYLSULFOXIDE-d6) δ [ppm]: −0.007 (0.49), 1.357(3.90), 2.174 (9.22), 2.184 (9.44), 2.250 (1.11), 3.982 (0.59), 3.999(4.28), 4.013 (14.94), 4.026 (5.89), 4.046 (1.15), 4.130 (1.63), 4.149(8.42), 4.156 (7.67), 4.163 (16.00), 4.177 (5.60), 4.194 (0.68), 12.355(2.94).

Intermediate 3244-chloro-6-{3,5-dimethyl-4-[2-(trifluoromethyl)-1,3-dioxolan-2-yl]-1H-pyrazol-1-yl}pyrimidine

Under an argon atmosphere,3,5-dimethyl-4-[2-(trifluoromethyl)-1,3-dioxolan-2-yl]-1H-pyrazole (5.19g, 95% purity, 20.9 mmol) was dissolved in N,N-dimethylformamide (47 mL)and 4,6-dichloropyrimidine (4.35 g, 29.2 mmol) and cesium carbonate(9.52 g, 29.2 mmol) was added. The reaction mixture was stirred atambient temperature overnight. It was then quenched by addition of waterand brine and the precipitated solid was collected by filtration, washedwith water and dried under high-vacuum to yield the desired product(7.18 g, 90% purity, 89% yield) that was used in the next step withoutfurther purification.

LC-MS (method 11): R_(t)=1.54 min; MS (ESIpos): m/z=349 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: −0.008 (0.83), 0.008 (0.85), 1.356(0.67), 2.145 (1.05), 2.216 (0.98), 2.309 (16.00), 2.330 (0.93), 2.670(0.48), 2.772 (13.50), 2.812 (0.58), 4.012 (0.51), 4.089 (0.71), 4.107(2.69), 4.124 (1.27), 4.147 (0.48), 4.163 (0.58), 4.223 (1.59), 4.231(1.41), 4.241 (3.06), 4.259 (0.95), 7.949 (4.03), 7.951 (4.03), 8.965(3.75), 8.967 (3.70).

Intermediate 325 1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-ylmethyl carbonate

Under an argon atmosphere,1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-ol (750 mg, 3.34mmol) was dissolved in N,N-dimethylformamide (10 mL),N,N-diisopropylethylamine (1.7 mL, 10 mmol) was added, followed byaddition of methyl carbonochloridate (520 μL, 6.7 mmol). The reactionmixture was stirred at ambient temperature for 5 h. Water was added andthe precipitated solid was collected by filtration, washed further withwater and dried under high-vacuum to yield the desired product (874 mg,92% yield).

LC-MS (method 11): R_(t)=1.31 min; MS (ESIpos): m/z=283 [M+H]⁺

¹H NMR (400 MHz, DIMETHYLSULFOXIDE-d₆) δ ppm: 2.17 (s, 3H), 2.56 (s,3H), 3.89 (s, 3H), 7.93 (s, 1H), 8.93 (s, 1H).

Intermediate 326 1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-ylmethylcarbamate

Under an argon atmosphere,1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-ol (750 mg, 3.34mmol) was dissolved in N,N-dimethylformamide (10 mL),N,N-diisopropylethylamine (1.7 ml, 10 mmol) was added, followed byaddition of methylcarbamyl chloride (624 mg, 6.68 mmol). The reactionmixture was stirred at ambient temperature for 5 h. Water was added andthe precipitated solid was collected by filtration, washed with waterand dried under high-vacuum to yield the desired product (844 mg, 89%yield).

LC-MS (method 11): R_(t)=1.09 min; MS (ESIpos): m/z=282 [M+H]⁺

¹H NMR (400 MHz, DIMETHYLSULFOXIDE-d₆) δ ppm: 2.13 (s, 3H), 2.51 (s,3H), 2.68 (d, J=4.65 Hz, 3H), 7.74-7.83 (m, 1H), 7.90 (s, 1H), 8.90 (s,1H).

Intermediate 327 1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yldimethylcarbamate

Under an argon atmosphere,1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-ol (750 mg, 3.34mmol) was dissolved in N,N-dimethylformamide (20 mL) andN,N-diisopropylethylamine (1.7 ml, 10 mmol) was added, followed byaddition of dimethylcarbamyl chloride (610 μl, 6.7 mmol). The reactionmixture was stirred at ambient temperature for 6 h. As only littleconversion was observed by LC-MS, N,N-dimethylaminopyridine (40.8 mg,334 μmol) was added and the reaction mixture was stirred overnight atambient temperature. Water was added and the precipitated solid wascollected by filtration, washed with water and dried under high-vacuumto yield the desired compound (802 mg, 80% yield).

LC-MS (method 9): R_(t)=0.96 min; MS (ESIpos): m/z=296 [M+H]⁺

¹H-NMR (400 MHz, DIMETHYLSULFOXIDE-d6) δ [ppm]: 2.131 (16.00), 2.521(15.90), 2.929 (9.90), 3.078 (10.13), 7.907 (3.99), 8.903 (4.05).

Intermediate 328 tert-butyl{4-[5-amino-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-3-yl]phenyl}methylcarbamate

To tert-butyl [4-(2-cyanopropanoyl)phenyl]methylcarbamate (1.03 g, 3.58mmol) in 2-propanol (9.3 ml, 120 mmol) at an internal temperature of 80°C. was slowly added oxalic acid(2-methoxyethyl)hydrazine (1:1) (710 mg,3.94 mmol) and the reaction heated at reflux for 4 h. The cooledreaction was filtered and concentrated in vacuo, the residue dissolvedin ethylacetate, basified with a saturated aqueous solution of sodiumcarbonate extracted two times with ethyl acetate. The combined organicphases were washed with a saturated aqueous solution of sodium chloride,dried with sodium sulfate and concentrated in vacuo. The crude productwas purified by flash-chromatography on silica gel (gradient 15%ethylacetate in cyclohexane to 100% ethylacetate, column: Biotage SNAPUltra 50 g). The resultant product was stirred in a mixture of pentaneand methyl tert-butyl ether and then filtered to yield 818 mg (100%purity, 63% yield) of the desired product.

LC-MS (Method 9): R_(t)=0.87 min; MS (ESIpos): m/z=361 [M+H]⁺

¹H-NMR (500 MHz, DMSO-d6) δ [ppm]: 1.399 (16.00), 1.987 (7.80), 3.189(8.33), 3.253 (10.79), 3.614 (0.96), 3.626 (2.18), 3.638 (1.01), 4.055(0.96), 4.067 (1.89), 4.078 (0.84), 4.872 (2.28), 7.250 (1.72), 7.254(0.58), 7.264 (0.70), 7.267 (1.87), 7.526 (2.21), 7.530 (0.66), 7.539(0.69), 7.543 (1.84).

Intermediate 3291-(2-methoxyethyl)-4-methyl-3-[4-(methylamino)phenyl]-1H-pyrazol-5-amine

To tert-butyl{4-[5-amino-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-3-yl]phenyl}methylcarbamate(816 mg, 2.26 mmol) in 1,4-dioxane (8.3 ml) was added 4N HCl in dioxane(4.2 ml, 4.0 M, 17 mmol) and the reaction stirred for 2 hat roomtemperature. Additional 4N HCl in dioxane (1.1 ml, 4.0 M, 4.4 mmol) andthe reaction stirred for a further 3 h. The reaction mixture was dilutedwith a saturated aqueous solution of sodium bicarbonate andethylacetate, the aqueous phase extracted twice with ethylacetate andthe combined organic phases dried with sodium sulfate. The organic phasewas concentrated in vacuo to yield 650 mg (91% purity, 100% yield) ofthe desired product.

LC-MS (Method 10): R_(t)=0.84 min; MS (ESIpos): m/z=261 [M+H]⁺

¹H-NMR (500 MHz, DMSO-d6) δ [ppm]: 1.174 (0.67), 1.932 (12.51), 1.988(1.30), 2.674 (5.86), 2.684 (5.80), 3.250 (16.00), 3.567 (9.19), 3.588(1.67), 3.600 (3.76), 3.611 (1.79), 4.006 (1.75), 4.018 (3.36), 4.030(1.53), 4.036 (0.41), 4.737 (3.84), 5.597 (0.87), 5.607 (0.86), 6.518(3.04), 6.536 (3.14), 7.300 (3.26), 7.317 (3.02).

Intermediate 3301,4-dimethyl-3-(6-methylpyridin-3-yl)-1H-pyrazol-5-amine

To (2R)-2-methyl-3-(6-methylpyridin-3-yl)-3-oxopropanenitrile (500 mg,2.87 mmol) in 2-propanol (7.5 ml, 97 mmol) at an internal temperature of80° C. was slowly added methylhydrazine (170 μl, 3.2 mmol) and thereaction heated at reflux overnight. The cooled reaction wasconcentrated in vacuo, the residue dissolved in water and solid sodiumhydrogen carbonate added until the solution was pH 7. The aqueoussolution was extracted three times with ethyl acetate and the combinedorganic phases dried with sodium sulfate and concentrated in vacuo. Thecrude product was purified by flash-chromatography on silica gel(dichloromethane:methanol 20:1, column: Biotage SNAP Ultra 50 g) toyield 233 mg (100% purity, 40% yield) of the desired product. Theproduct is unstable when analysed by LCMS.

LC-MS (Method 21): R_(t)=0.94 min; MS (ESIpos): m/z=203 [M+H]⁺

¹H-NMR (500 MHz, DMSO-d6) δ [ppm]: 1.979 (16.00), 2.463 (11.28), 3.317(12.54), 4.994 (3.33), 7.230 (1.59), 7.246 (1.67), 7.792 (1.36), 7.796(1.35), 7.808 (1.26), 7.813 (1.25), 8.626 (1.66), 8.629 (1.66).

Intermediate 3311-(cyclopropylmethyl)-4-methyl-3-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-5-amine

A solution of2-methyl-3-oxo-3-[6-(trifluoromethyl)pyridin-3-yl]propanenitrile (3.16g, 13.8 mmol) in ethanol (30 ml) was treated with(cyclopropylmethyl)hydrazine-hydrogen chloride (1/2) (4.40 g, 27.7 mmol)and stirred overnight at 95° C. After cooling to ambient temperature themixture was diluted with saturated sodium bicarbonate solution and theethanol was removed under reduced pressure. The remaining aqueous wasextracted with ethyl acetate (3×). The combined organics were washedwith brine, dried over sodium sulfate and concentrated under reducedpressure to yield 3.75 g of the desired product (92%).

LC-MS (Method 10): R_(t)=1.66 min; MS (ESIpos): m/z=297 [M+H]⁺

¹H-NMR (500 MHz, DMSO-d6) δ [ppm]: 0.364 (0.56), 0.374 (1.87), 0.377(1.75), 0.384 (2.03), 0.386 (1.79), 0.394 (0.82), 0.440 (0.90), 0.448(1.70), 0.451 (1.40), 0.456 (1.04), 0.461 (0.97), 0.464 (1.79), 0.467(1.29), 0.477 (0.51), 1.222 (0.45), 1.224 (0.40), 1.228 (0.44), 1.238(0.71), 1.247 (0.40), 2.064 (16.00), 2.078 (0.52), 3.859 (3.51), 3.873(3.41), 5.102 (3.86), 7.882 (1.76), 7.883 (1.73), 7.898 (1.93), 8.213(1.04), 8.216 (0.99), 8.230 (0.90), 8.233 (0.88), 8.985 (1.80), 8.989(1.72).

Intermediate 3323-[4-(difluoromethyl)phenyl]-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-amine

A solution of 3[4-(difluoromethyl)phenyl]-2-methyl-3-oxopropanenitrile(3.10 g, 14.8 mmol) in 2-propanol (31 ml) was treated with oxalicacid-(2-methoxyethyl)hydrazine (1/1) (3.47 g, 19.3 mmol) and stirredovernight at 95° C. After cooling to ambient temperature the mixture wasconcentrated under reduced pressure. The remaining residue was resolvedin water and ethyl acetate. The organic phase was washed with water andbrine, dried over sodium sulfate and concentrated under reducedpressure. The crude product was purified by flash-chromatography(column: SNAP Ultra 50 g, solvent: dichloromethane/methanol 99:1 to90/10) and subsequent preparative HPLC (method: column: Reprosil C18; 10μm; 125×30 mm/flow: 50 ml/min/eluent: A=H₂O (0.01% HCOOH),B=acetonitrile/gradient: 0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75min=100% B, 19.75-23.00 min=90% B) to yield 6.2 g (quant.) of thedesired product which was used without any further purification.

Intermediate 3333-(5-fluoropyridin-2-yl)-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-amine

A solution of 3-(5-fluoropyridin-2-yl)-2-methyl-3-oxopropanenitrile(1.50 g, 8.42 mmol) in ethanol (18 ml) was treated with oxalicacid-(2-methoxyethyl)hydrazine (1/1) (3.03 g, 16.8 mmol) and stirredovernight at 95° C. After cooling to ambient temperature the mixture wasconcentrated under reduced pressure and the remaining residue wassuspended in water and extracted with ethyl acetate (3×). The combinedorganics were washed with water and brine, dried over sodium sulfate andconcentrated under reduced pressure. The crude product was purified byflash-chromatograph (column: SNAP Ultra 10 g, solvent:dichloromethane/methanol 100/0 to 96/4) and subsequent preparative HPLC(method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 50 ml/min/eluent:A=H2O (0.01% HCOOH), B=acetonitrile/gradient: 0.00-5.00 min=10% B, 6.50min=20% B, 17.0-19.75 min=100% B, 19.75-23.00 min=90% B) to yield 509 mgof the desired product (24%).

LC-MS (Method 11): R_(t)=0.84 min; MS (ESIpos): m/z=251 [M+H]⁺

Intermediate 334

N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-(5,6-dihydropyrrolo[3,4-c]pyrazol-1(4H)-yl)pyrimidin-4-amine

tert-butyl1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate(71.5 mg, 135 μmol) was dissolved in a mixture of trifluoroacetic acidand dichloromethane (2:1, 1.5 ml) and stirred at room temperature for 2h. The reaction was concentrated in vacuo, and the residue redissolvedin ethylacetate. The organic phase was washed with a saturated aqueoussolution of sodium bicarbonate. dried with sodium sulfate andconcentrated in vacuo. The crude product was purified byflash-chromatography on silica gel (Gradient 20:1 to 15:1dichloromethane:methanol, column: Biotage SNAP Ultra 10 g) to yield 30.3mg (100% purity, 52% yield) of the desired product.

LC-MS (Method 9): R_(t)=0.74 min; MS (ESIpos): m/z=431 [M+H]⁺

¹H-NMR (500 MHz, DMSO-d6) δ [ppm]: 0.281 (1.89), 0.411 (2.07), 0.426(2.05), 1.181 (0.83), 1.230 (0.30), 1.905 (0.47), 2.004 (16.00), 3.835(1.80), 3.877 (2.74), 4.294 (3.98), 4.771 (0.19), 7.257 (1.94), 7.274(3.74), 7.292 (1.97), 7.560 (0.35), 7.733 (1.76), 8.466 (0.35), 9.519(0.30).

Intermediate 335N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-(5,6-dihydropyrrolo[3,4-c]pyrazol-2(4H)-yl)pyrimidin-4-amine

tert-butyl2-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-2,6-dihydropyrrolo[3,4-c]pyrazole-5(4H)-carboxylate(75.0 mg, 141 μmol) was dissolved in a mixture of trifluoroacetic acidand dichloromethane (2:1, 1.5 ml) and stirred at room temperature for 2h. The reaction was concentrated in vacuo, and the residue redissolvedin ethylacetate. The organic phase was washed with a saturated aqueoussolution of sodium bicarbonate. dried with sodium sulfate andconcentrated in vacuo. The crude product was purified byflash-chromatography on silica gel (15:1 dichloromethane:methanol,column: Biotage SNAP Ultra 10 g) to yield 36.6 mg (100% purity, 60%yield) of the desired product.

LC-MS (Method 9): R_(t)=0.72 min; MS (ESIneg): m/z=429 [M−H]⁻

¹H-NMR (500 MHz, DMSO-d6) δ [ppm]: 0.292 (1.66), 0.412 (1.87), 0.428(1.86), 1.183 (0.79), 1.233 (0.27), 1.353 (0.14), 1.905 (0.24), 2.014(16.00), 3.846 (4.77), 4.393 (0.17), 7.260 (1.91), 7.278 (3.89), 7.295(2.08), 7.745 (1.60), 8.232 (3.61), 8.395 (0.20), 8.464 (0.35), 9.469(0.28).

Intermediate 336 ethyl 6-(trifluoromethyl)pyridine-3-carboxylatehydrogen chloride

6-(trifluoromethyl)pyridine-3-carboxylic acid (10.0 g, 52.3 mmol) wastreated with thionyl chloride (35 ml, 480 mmol) and refluxed for 2hours. After cooling to ambient temperature the mixture was concentratedunder reduced pressure and the remaining residue was resolved inethanol. The resulting solution was refluxed overnight. After cooling toambient temperature 11.8 g of the desired product (88%) were obtainedwhich were used without any further purification.

LC-MS (Method 10): R_(t)=1.79 min; MS (ESIpos): m/z=220 [M+H]⁺

Intermediate 3372-methyl-3-oxo-3-[6-(trifluoromethyl)pyridin-3-yl]propanenitrile

A solution of ethyl 6-(trifluoromethyl)pyridine-3-carboxylate-hydrogenchloride (1/1) (11.8 g, 46.2 mmol) and propanenitrile (4.9 ml, 69 mmol)in tertrahydrufuran (120 ml, 1.4 mol) was treated with a solution oflithium bis(trimethylsilyl)amide (120 ml, 1.0 M, 120 mmol). The mixturewas stirred overnight at ambient temperature. The mixture was dilutedwith water and extracted once with ethyl acetate. The organic phase wasdiscarded. The aqueous phase was acidified with 10% citric acid solutionand extracted with dichloromethane (2×). The combined organics werewashed with water, dried over sodium sulfate and concentrated underreduced pressure to yield 9.25 g (76%) of the desired product.

LC-MS (Method 9): R_(t)=0.78 min; MS (ESIpos): m/z=229 [M+H]⁺

¹H-NMR (500 MHz, DMSO-d6) δ [ppm]: 0.018 (0.46), 1.179 (0.59), 1.507(0.56), 1.521 (0.55), 1.701 (3.04), 1.916 (2.17), 1.925 (16.00), 1.992(1.08), 3.350 (0.48), 8.043 (2.57), 8.060 (2.57), 8.268 (1.52), 8.272(1.47), 8.284 (1.30), 8.288 (1.24), 8.944 (2.52).

Intermediate 3384-methyl-3-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-5-amine

A solution of2-methyl-3-oxo-3-[6-(trifluoromethyl)pyridin-3-yl]propanenitrile (6.05g, 26.5 mmol) in ethanol (57 ml) was treated with hydrazinewater (1/1)(2.6 ml, 53 mmol) and stirred at 95° C. overnight. After cooling toambient temperature the mixture was diluted with saturated sodiumcarbonate solution and enthanol was removed under reduced pressure. Theremaining aqueous was extracted with ethyl acetate (3×). The combinedorganics were washed with brine, dried over sodium sulfate and thesolvent was removed under reduced pressure to yield 6.4 g (100%) of thedesired product.

LC-MS (Method 10): R_(t)=1.15 min; MS (ESIpos): m/z=243 [M+H]⁺

Intermediate 3392-{4-methyl-3-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-5-yl}-1H-isoindole-1,3(2H)-dione

A solution of4-methyl-3-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-5-amine (6.40 g,26.4 mmol) and 2-benzofuran-1,3-dione (5.87 g, 39.6 mmol) in acetic acid(75 ml) was stirred for 2 days at 125° C. After cooling to ambienttemperature the mixture was evaporated, the residue was resolved inwater and ethyl acetate. The organic phase was washed with brine, driedover sodium sulfate and the solvent was removed under reduced pressureto yield 11.6 g of the desired product (72%).

LC-MS (Method 9): R_(t)=0.91 min; MS (ESIpos): m/z=373 [M+H]⁺

¹H-NMR (500 MHz, DMSO-d6) δ [ppm]: −0.007 (0.58), 0.006 (0.46), 1.234(0.80), 2.076 (1.06), 2.101 (16.00), 7.578 (2.71), 7.584 (2.82), 7.589(2.61), 7.596 (3.72), 7.603 (0.50), 7.658 (0.50), 7.666 (3.37), 7.673(2.44), 7.678 (2.49), 7.684 (2.22), 7.957 (5.80), 7.963 (6.59), 7.968(6.75), 7.974 (8.77), 7.982 (1.72), 8.003 (1.48), 8.009 (1.77), 8.015(2.63), 8.024 (6.92), 8.030 (5.92), 8.034 (5.42), 8.040 (4.40), 8.068(2.02), 8.085 (3.58), 8.090 (2.02), 8.096 (1.61), 8.102 (1.33), 8.347(2.79), 8.363 (2.50), 9.086 (4.01), 13.773 (0.84).

Intermediate 3402-{1,4-dimethyl-3-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-5-yl}-1H-isoindole-1,3(2H)-dione

A solution of2-{4-methyl-3-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-5-yl}-1H-isoindole-1,3(2H)-dione (11.6 g, 31.2 mmol) in dimethylformamide (100 ml, 1.3 mol)was treated with cesium carbonate (20.3 g, 62.3 mmol) and iodomethane(3.9 ml, 62 mmol). The mixture was stirred overnight. The mixture wasfiltered and poured onto saturated ammonium chloride solution. Themixture was extracted with ethyl acetate (3×). The combined organicswere washed with water, brine, dried over sodium sulfate andconcentrated under reduced pressure. The crude product was purified bypreparative HPLC (column: Kinetex C18 5 μM 100×30 mm, flow: 80 mL/min,solvent: A=water, B=acetonitrile, C=acetonitrile, gradient: 0.00-0.95min A/B/C 71/4/25; 0.95-5.00 min to A/B/C 46/4/50; 5.00-5.20 min toA/B/C 5/4/91 until 5.70 min; 5.70-5.90 min to A/B/C 71/4/25 until 7.30min) to yield 5.42 g (45%) of the desired product along with itsregioisomer (2.57 g, 21%).

LC-MS (Method 10): R_(t)=1.95 min; MS (ESIpos): m/z=387 [M+H]⁺

¹H-NMR (500 MHz, DMSO-d6) δ [ppm]: 2.075 (0.70), 2.113 (15.68), 3.809(16.00), 7.976 (2.84), 7.982 (4.73), 7.987 (2.87), 7.993 (3.92), 7.997(2.56), 8.046 (0.60), 8.054 (3.93), 8.060 (2.83), 8.065 (2.73), 8.071(2.46), 8.360 (1.27), 8.364 (1.21), 8.376 (1.12), 8.380 (1.06), 9.105(2.20), 9.109 (2.09).

Intermediate 3412-{1,4-dimethyl-5-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-3-yl}-1H-isoindole-1,3(2H)-dione

A solution of2-{4-methyl-3-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-5-yl}-1H-isoindole-1,3(2H)-dione(11.6 g, 31.2 mmol) in dimethylformamide (100 ml, 1.3 mol) was treatedwith cesium carbonate (20.3 g, 62.3 mmol) and iodomethane (3.9 ml, 62mmol). The mixture was stirred overnight. The mixture was filtered andpoured onto saturated ammonium chloride solution. The mixture wasextracted with ethyl acetate (3×). The combined organics were washedwith water, brine, dried over sodium sulfate and concentrated underreduced pressure. The crude product was purified by preparative HPLC(column: Kinetex C18 5 μM 100×30 mm, flow: 80 mL/min, solvent: A=water,B=acetonitrile, C=acetonitrile, gradient: 0.00-0.95 min A/B/C 71/4/25;0.95-5.00 min to A/B/C 46/4/50; 5.00-5.20 min to A/B/C 5/4/91 until 5.70min; 5.70-5.90 min to A/B/C 71/4/25 until 7.30 min) to yield 2.57 g(21%) of the desired product along with its regioisomer (5.42 g, 45%).

LC-MS (Method 10): R_(t)=1.84 min; MS (ESIpos): m/z=387 [M+H]⁺

Intermediate 3421,4-dimethyl-3-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-5-amine

A solution of2-{1,4-dimethyl-3-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-5-yl}-1H-isoindole-1,3(2H)-dione(5.42 g, 14.0 mmol) in ethanol (190 ml, 3.3 mol) was treated withhydrazine monohydrate (3.4 ml, 70 mmol) and stirred at 90° C. overnight.After cooling to ambient temperature the mixture was diluted with waterand extracted with ethyl acetate (3×). The combined organics were washedwith 1M sodium hydrogen carbonate solution and brine, dried over sodiumsulfate and concentrated under reduced pressure to yield 3.66 g (99%) ofthe desired product.

LC-MS (Method 10): R_(t)=1.32 min; MS (ESIpos): m/z=257 [M+H]⁺

¹H-NMR (500 MHz, DMSO-d6) δ [ppm]: 2.058 (16.00), 3.328 (15.45), 5.138(4.70), 7.878 (2.07), 7.894 (2.26), 8.199 (1.30), 8.202 (1.22), 8.215(1.15), 8.218 (1.08), 8.975 (2.24), 8.977 (2.13).

Intermediate 3431,4-dimethyl-5-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-3-amine

A solution of2-{1,4-dimethyl-5-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-3-yl}-1H-isoindole-1,3(2H)-dione(2.57 g, 6.65 mmol) in ethanol (91 ml, 1.6 mol) was treated withhydrazine monohydrate (1.6 ml, 33 mmol) and stirred at 90° C. overnight.After cooling to ambient temperature the mixture was diluted with waterand extracted with ethyl acetate (3×). The combined organics were washedwith saturated sodium hydrogen carbonate solution and brine, dried oversodium sulfate and concentrated under reduced pressure to yield 1.78 g(98%) of the desired product.

LC-MS (Method 10): R_(t)=1.26 min; MS (ESIpos): m/z=257 [M+H]⁺

¹H-NMR (500 MHz, DMSO-d6) δ [ppm]: 1.830 (16.00), 2.063 (0.44), 2.282(0.51), 3.065 (0.55), 3.333 (13.10), 3.748 (0.45), 3.861 (0.51), 3.906(1.09), 4.604 (3.87), 8.014 (1.69), 8.031 (2.30), 8.114 (1.27), 8.118(1.22), 8.130 (0.90), 8.134 (0.88), 8.800 (1.96), 8.804 (1.88).

Intermediate 3444-[5-amino-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile

A solution of 4-(2-cyanopropanoyl)benzonitrile (2.73 g, 14.8 mmol) inethanol (55 ml) was treated with oxalic acid(2-methoxyethyl)hydrazine(1/1) (5.33 g, 29.6 mmol) and triethylamine (4.5 ml, 33 mmol). Themixture was stirred overnight at 95° C. After cooling to ambienttemperature the mixture was diluted with saturated sodium carbonatesolution. Ethanol was removed under reduced pressure. The aqueous wasextracted with ethyl acetate (3×). The combined organics were washedwith brine, dried over sodium sulfate and concentrated under reducedpressure to yield the desired product (3.57 g, 87%).

LC-MS (Method 10): R_(t)=1.33 min; MS (ESIpos): m/z=257 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: 2.015 (1.40), 2.031 (13.36), 2.523(0.40), 3.250 (16.00), 3.262 (1.84), 3.628 (1.80), 3.643 (4.13), 3.657(2.00), 4.080 (0.46), 4.088 (1.91), 4.103 (3.66), 4.117 (1.65), 4.867(0.46), 5.001 (3.92), 7.588 (0.95), 7.775 (1.17), 7.779 (0.60), 7.796(6.18), 7.807 (6.11), 7.824 (0.57), 7.829 (1.10).

Intermediate 3451-(6-{[3-(5-fluoropyridin-2-yl)-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylicacid

A solution of ethyl1-(6-{[3-(5-fluoropyridin-2-yl)-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(68.6 mg, 139 μmol) in tetrahydrofuran (2.0 ml, 25 mmol) was treatedwith a aqueous solution of lithium hydroxide (690 μl, 1.0 M, 690 μmol)and refluxed for 2 days. After cooling to ambient temperature themixture was diluted with water and acidified with 10% citric acidsolution (pH=6). The aqueous was extracted with ethyl acetate (3×). Thecombined organics were dried over sodium sulfate and concentrated underreduced pressure. The residue was suspended in acetonitrile, theoccurring precipitate was collected by filtration washed withacetonitrile and dried to yield 32.2 mg (50%) of the desired product.

LC-MS (Method 10): R_(t)=1.57 min; MS (ESIpos): m/z=467 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: 2.144 (16.00), 2.327 (5.77), 2.366(2.80), 2.523 (12.62), 2.669 (4.78), 2.710 (1.73), 2.900 (13.36), 3.146(3.71), 3.673 (3.46), 4.142 (1.48), 7.773 (1.57), 7.978 (1.32), 8.593(2.97), 8.600 (2.89), 9.495 (1.24), 12.632 (2.06).

Intermediate 3461-[6-({3-[4-(difluoromethyl)phenyl]-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3,5-dimethyl-1H-pyrazole-4-carboxylicacid

A solution of ethyl1-[6-({3-[4-(difluoromethyl)phenyl]-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3,5-dimethyl-1H-pyrazole-4-carboxylate(139 mg, 264 μmol) in tetrahydrofuran (3.0 ml, 37 mmol) was treated witha aqueous solution of lithium hydroxide (1.3 ml, 1.0 M, 1.3 mmol) andthe mixture was refluxed for 2 days. After cooling to ambienttemperature the mixture was diluted with water and acidified with 10%citric acid solution (pH=6). The aqueous was extracted with ethylacetate (3×). The combined organics were dried over sodium sulfate andconcentrated under reduced pressure. The residue was triturated withacetonitrile to yield 92.7 mg (68%) of the desired product.

LC-MS (Method 10): R_(t)=1.75 min; MS (ESIpos): m/z=498 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: 2.048 (16.00), 2.360 (2.63), 2.907(13.48), 3.152 (5.46), 3.661 (1.97), 3.675 (4.11), 3.689 (2.22), 4.143(1.60), 6.938 (1.37), 7.078 (2.95), 7.218 (1.28), 7.637 (2.99), 7.657(3.81), 7.842 (3.08), 7.861 (2.66), 8.541 (0.83), 9.502 (1.27), 12.639(0.67).

SPECIFIC EXAMPLES Example 16-(3,5-dimethyl-1H-pyrazol-1-yl)-N-[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]pyrimidin-4-amine

To a solution of 4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine(231 mg, 1.05 mmol) in 1,4-dioxane (3.0 mL) sodium phenoxide (167 mg,1.44 mmol) was added and argon was poured through the mixture.Tris(dibenzylideneacetone)dipalladium(0) (11.4 mg, 12.5 μmol), Xantphos(16.6 mg, 28.8 mmol) and4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (200 mg, 959 μmol)were added to the mixture. The reaction vessel was capped and themixture was stirred at 80° C. overnight. After cooling to roomtemperature the resulting mixture was separated via preparative HPLC(Column: Reprosil C18; 10 μm; 125×30 mm/Flow: 50 ml/min/Eluent: A=water(0.01% formic acid), B=acetonitrile/Gradient: 0.00-5.00 min=10% B, 6.50min=20% B, 17.0-19.75 min=100% B, 19.75-23.00 min=90% B) to yield 180 mgof the desired product (48% yield).

LC-MS (method 10): R_(t)=2.16 min; MS (ESIpos): m/z=392 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.89 (t, 3H), 2.18 (s, 3H), 2.31 (q,2H), 2.62 (s, 3H), 3.65 (s, 3H), 6.13 (s, 1H), 7.31-7.42 (m, 3H), 7.52(dd, 2H), 8.44 (s, 1H), 9.33 (s, 1H).

Example 26-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]-N-[4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]pyrimidin-4-amine

A solution of4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (128mg, 523 μmol) and 4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-amine (215 mg,1.05 mmol) in NMP (850 μL) was treated with concentrated aqueoushydrochloric acid (130 μL, 12 M, 1.6 mmol). The resulting mixture wasstirred for 1 hour at 200° C. in the microwave. After cooling to roomtemperature the crude product was purified by preparative HPLC (method:C18, 250×30, flow 50 ml/min, Runtime: 340 min, detection at 210 nm,gradient 40% acetonitrile (6 min)→95% acetonitrile (28 min)→95%acetonitrile (38 min)→34% acetonitrile (39 min), water+0.05% formicacid) to yield 53.5 mg of the desired product (25% yield).

LC-MS (method 10): R_(t)=2.12 min; MS (ESIpos): m/z=414 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (2.85), 0.008 (2.16), 0.994(3.88), 1.013 (8.59), 1.032 (4.11), 2.073 (0.64), 2.276 (16.00), 2.328(0.69), 2.574 (0.96), 2.670 (0.69), 6.762 (4.80), 7.342 (2.38), 7.365(5.05), 7.387 (2.83), 7.463 (1.14), 7.594 (2.76), 7.607 (3.17), 7.616(2.81), 7.629 (2.38), 7.696 (1.93), 7.832 (3.66), 7.968 (1.56), 8.483(3.08), 9.552 (2.16), 12.865 (2.51).

Example 3N-[4-chloro-3-(2,4-difluorophenyl)-1H-pyrazol-5-yl]-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A solution of4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (116 mg,477 μmol) and 4-chloro-3-(2,4-difluorophenyl)-1H-pyrazol-5-amine (121mg, 525 μmol) in 1-methoxy-2-propanol (2.2 mL) was treated with aqueoushydrochloric acid in 1,4-dioxane (360 μl, 4.0 M, 1.4 mmol). The reactionvessel was capped and the mixture was shaken overnight at 120° C. Aftercooling to room temperature the resulting mixture was purified bypreparative HPLC (method 4) to yield 39.9 mg of the desired compound(17% yield).

LC-MS (method 9): R_(t)=1.24 min; MS (ESIpos): m/z=436 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 2.20-2.27 (m, 3H), 2.62-2.69 (m, 3H),7.15-7.42 (m, 2H), 7.50 (br s, 1H), 7.58-7.78 (m, 1H), 8.50-8.58 (m,1H), 9.74 (br s, 1H).

Example 4 ethyl1-(6-{[4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

A solution of6-chloro-N-[4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]pyrimidin-4-amine(100 mg, 315 μmol) and ethyl 3,5-dimethyl-1H-pyrazole-4-carboxylate (106mg, 629 μmol, CAS 35691-93-1) in DMF (2.0 mL) was treated with caesiumcarbonate (308 mg, 944 μmol). The reaction mixture was stirred at 160°C. overnight. After cooling to room temperature the mixture was purifiedby preparative HPLC (method: column: Reprosil C18; 10 μm; 125×30mm/flow: 50 ml/min/eluent: A=water (0.01% formic acid),B=acetonitrile/gradient: 0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75min=100% B, 19.75-23.00 min=90% B) to afford 84.6 mg (60% yield) of thefinal product.

LC-MS (method 10): R_(t)=2.16 min; MS (ESIpos): m/z=450 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.008 (0.94), 0.999 (4.17), 1.017(9.28), 1.031 (3.06), 1.036 (4.41), 1.046 (2.08), 1.287 (5.52), 1.304(11.52), 1.322 (5.67), 2.366 (15.89), 2.575 (0.97), 2.895 (16.00), 4.226(1.64), 4.243 (5.08), 4.261 (5.03), 4.279 (1.58), 7.336 (1.15), 7.356(1.94), 7.376 (1.15), 7.452 (0.67), 7.594 (1.49), 7.608 (1.96), 8.536(2.40), 9.553 (1.12), 12.835 (1.71).

Example 56-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-[4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]pyrimidin-4-amine

A solution of6-chloro-N-[4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]pyrimidin-4-amine(69.5 mg, 219 ∞mol) and 4-chloro-3,5-dimethyl-1H-pyrazole (143 mg, 1.09mmol) in NMP (2.5 mL) was treated with DBU (98 μL, 660 μmol). Thereaction mixture was stirred 40 minutes at 190° C. under microwaveradiation. After cooling to room temperature the crude product waspurified by preparative HPLC (method: column: Reprosil C18; 10 μm;125×30 mm/flow: 50 ml/min/eluent: A=water (0.01% formic acid),B=acetonitrile/gradient: 0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75min=100% B, 19.75-23.00 min=90% B) to yield 14.8 mg (16% yield) of thedesired product.

LC-MS (method 9): R_(t)=1.21 min; MS (ESIpos): m/z=412 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (1.44), 0.008 (1.39), 0.993(3.49), 1.012 (7.57), 1.030 (3.64), 1.234 (0.61), 2.073 (0.57), 2.204(14.12), 2.524 (2.22), 2.570 (0.99), 2.644 (16.00), 2.670 (0.54), 7.339(1.81), 7.361 (3.79), 7.383 (2.15), 7.433 (1.23), 7.588 (2.18), 7.602(2.54), 7.610 (2.31), 7.623 (1.89), 8.487 (2.29), 9.454 (2.31), 12.834(2.49).

Example 6N-[4-chloro-5-(2,4-difluorophenyl)-1H-pyrazol-3-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A solution of 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (87.6mg, 420 μmol) and 4-chloro-3-(2,4-difluorophenyl)-1H-pyrazol-5-amine(106 mg, 462 μmol) in 1-methoxy-2-propanol (2.0 mL) was treated withhydrochloric acid in 1,4-dioxane (310 μL, 4.0 M, 1.3 mmol). The reactionmixture was stirred overnight at 120° C. The resulting crude product waspurified by preparative HPLC (10-70% acetonitrile/water with 0.1% TFA)to yield 31.5 mg (17% yield) of the final product.

LC-MS (method 10): R_(t)=2.03 min; MS (ESIpos): m/z=402 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.149 (0.53), −0.008 (4.64), 0.008(3.90), 0.146 (0.50), 2.187 (13.27), 2.328 (0.80), 2.366 (0.59), 2.523(2.95), 2.635 (16.00), 2.670 (0.93), 2.710 (0.63), 6.147 (2.76), 7.306(0.90), 7.362 (1.18), 7.520 (0.63), 7.699 (0.68), 8.490 (1.22), 9.531(1.09), 13.433 (0.91).

Example 7

N-[4-cyclopropyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A solution of 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (50.0mg, 240 μmol) and 4-cyclopropyl-5-(4-fluorophenyl)-1H-pyrazol-3-amine(130 mg, 599 μmol) in DMSO (1.4 mL) was treated with phosphazen-baseP(2)-Et (220 μL, 650 μmol) and tBuBrettPhos Pd G3 (20.5 mg, 24.0 μmol).The resulting mixture was stirred for 1 hour at room temperature.Subsequently acetic acid was added and the crude product was purified bypreparative HPLC (method: C18, 250×30, flow 50 ml/min, Runtime: 340 min,detection at 210 nm, eluent: A=water (0.05% formic acid),B=acetonitrile, gradient 40% B/60% A (6 min)→95% B/5% A (28 min)→95%B/5% A (38 min)→34% B/76% A (39 min)) to yield 30.4 mg (33% yield) ofthe desired product.

LC-MS (method 10): R_(t)=2.07 min; MS (ESIpos): m/z=390 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (1.06), 0.008 (0.86), 0.232(2.38), 0.241 (2.50), 0.256 (0.75), 0.721 (1.82), 0.738 (2.04), 1.658(0.77), 1.665 (0.80), 1.678 (1.16), 2.172 (16.00), 2.630 (15.53), 6.125(3.46), 7.332 (1.78), 7.354 (4.20), 7.359 (2.92), 7.376 (2.06), 7.778(1.89), 7.792 (2.22), 7.800 (2.11), 7.814 (1.75), 8.454 (2.96), 9.144(2.66), 12.871 (2.35).

Example 86-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-[4-cyclopropyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]pyrimidin-4-amine

A solution of 4-cyclopropyl-3-(4-fluorophenyl)-1H-pyrazol-5-amine (220mg, 1.01 mmol) and4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (164 mg,675 μmol) in DMSO (3.5 mL) was treated with phosphazen-base P(2)-Et (610μl, 1.8 mmol) and tBuBrettPhos Pd G3 (57.7 mg, 67.5 μmol). The resultingmixture was stirred for 1 hour at room temperature. Subsequently aceticacid was added. The solution was directly purified by preparative HPLC(method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 45 ml/min/eluent:A=water (0.1% formic acid), B=acetonitrile/gradient: 0.00-4.25 min=20%B, 4.50 min=70% B, 15.50 min=85% B, 16.00-23.00 min=100% B, 23.00-27.00min=20% B) to yield 32.0 mg (7% yield) of the desired product.

LC-MS (method 11): R_(t)=1.58 min; MS (ESIpos): m/z=424 [M+H]⁺

¹H-NMR (600 MHz, DMSO-d₆) δ [ppm]: 0.005 (0.54), 0.230 (1.37), 0.727(1.15), 1.678 (0.75), 2.211 (8.98), 2.518 (0.58), 2.521 (0.58), 2.524(0.48), 2.649 (16.00), 3.978 (0.43), 5.762 (2.80), 7.358 (1.28), 7.372(0.95), 7.798 (1.10), 8.497 (1.28), 9.315 (0.78), 12.908 (0.72).

Example 9

N-[5-(2,4-difluorophenyl)-4-ethyl-1H-pyrazol-3-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A solution of 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (50.0mg, 240 μmol) and 5-(2,4-difluorophenyl)-4-ethyl-1H-pyrazol-3-amine (107mg, 479 μmol) in NMP (400 μL) was treated with concentrated aqueoushydrochloric acid (60 μL, 12 M, 710 mmol). The reaction mixture wasstirred for 1 hour at 120° C. under microwave radiation. After coolingto room temperature the crude mixture was purified by preparative HPLC(method: C18, 250×30, flow 50 ml/min, Runtime: 340 min, detection at 210nm, eluent: A=water (0.05% formic acid), B=acetonitrile, gradient 40%B/60% A (6 min)→95% B/5% A (28 min)→95% B/5% A (38 min)→34% B/76% A (39min)) to afford 10.1 mg (11% yield) of the desired product.

LC-MS (method 10): R_(t)=2.02 min; MS (ESIpos): m/z=396 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.008 (0.88), 0.909 (3.70), 0.928(8.31), 0.947 (3.83), 2.073 (2.26), 2.174 (16.00), 2.328 (0.42), 2.365(0.89), 2.381 (2.31), 2.399 (2.27), 2.417 (0.77), 2.627 (15.33), 2.670(0.40), 6.128 (4.10), 7.223 (0.56), 7.243 (1.07), 7.261 (0.63), 7.415(0.65), 7.437 (0.92), 7.462 (0.51), 7.530 (0.78), 7.551 (1.51), 7.568(1.51), 7.589 (0.68), 8.460 (3.14), 9.379 (0.47).

Example 106-(3,5-dimethyl-1H-pyrazol-1-yl)-N-(4-methyl-3-phenyl-1H-pyrazol-5-yl)pyrimidin-4-amine

A solution of 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (50.0mg, 240 μmol) and 4-methyl-3-phenyl-1H-pyrazol-5-amine (83.0 mg, 479μmol) in NMP (390 μL) was treated with concentrated aqueous hydrochloricacid (60 μl, 12 M, 720 μmol). The resulting mixture was stirred for 1hour at 200° C. under microwave radiation. After cooling to roomtemperature the crude mixture was purified using preparative (method:C18, 250×30, flow 50 ml/min, Runtime: 340 min, detection at 210 nm,eluent: A=water (0.05% formic acid), B=acetonitrile, gradient 40% B/60%A (6 min)→95% B/5% A (28 min)→95% B/5% A (38 min)→34% B/76% A (39 min))to yield 36.2 mg (44% yield) of the final product.

LC-MS (method 10): R_(t)=1.86 min; MS (ESIpos): m/z=346 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (1.55), 0.008 (1.45), 2.076(14.86), 2.171 (16.00), 2.627 (14.31), 6.124 (3.49), 7.404 (1.66), 7.422(1.29), 7.458 (1.28), 7.492 (1.94), 7.512 (3.51), 7.530 (1.95), 7.597(3.70), 7.615 (2.53), 8.458 (2.85), 9.376 (2.99), 12.826 (2.16).

Example 116-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-(4-methyl-5-phenyl-1H-pyrazol-3-yl)pyrimidin-4-amine

A solution of4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (128 mg,525 μmol) and 4-methyl-5-phenyl-1H-pyrazol-3-amine (100 mg, 577 μmol) inNMP (6.0 mL) was treated with hydrochloric acid in 1,4-dioxane (390 μL,4.0 M, 1.6 mmol). The reaction mixture was stirred for 2 hours at 190°C. under microwave radiation. After cooling to room temperature theresulting mixture was diluted with acetonitrile and water andsubsequently purified by preparative HPLC to afford 30.0 mg (15% yield)of the final product.

LC-MS (method 10): R_(t)=2.17 min; MS (ESIpos): m/z=380 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (1.97), 0.008 (1.60), 2.073(5.32), 2.079 (9.88), 2.210 (12.85), 2.519 (1.33), 2.524 (1.00), 2.647(16.00), 2.665 (0.42), 2.670 (0.62), 7.381 (0.59), 7.399 (1.59), 7.418(1.20), 7.487 (2.02), 7.506 (3.48), 7.525 (1.89), 7.602 (3.17), 7.621(2.25), 8.499 (3.08), 9.520 (2.08).

Example 126-(3,5-dimethyl-1H-pyrazol-1-yl)-N-[4-ethyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]pyrimidin-4-amine

To a solution of 4-ethyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-amine(116 mg, 527 μmol) in 1,4-dioxane (2.5 mL) sodium phenoxide (83.5 mg,719 μmol) was added and argon was poured through the mixture.Tris(dibenzylideneacetone)dipalladium(0) (5.49 mg, 5.99 μmol), Xantphos(8.32 mg, 14.4 μmol) and4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (100 mg, 479 μmol)were added to the mixture. The reaction vessel was capped and themixture was stirred at 80° C. in the microwave for 2 hours. Aftercooling to room temperature the resulting mixture was separated viapreparative HPLC (Column: Reprosil C18; 10 μm; 125×30 mm/Flow: 50ml/min/Eluent: A=water (0,01% formic acid), B=acetonitrile/Gradient:0.00-5.00 min=10% B, 6.50 min=20% B, 17.00-19.75 min=100% B, 19.75-23.00min=90% B) to yield 91 mg of still impure product. Further separation onpreparative HPLC (Method 1) yielded 48.8 mg of the desired product (25%yield).

LC-MS (method 10): R_(t)=2.13 min; MS (ESIpos): m/z=392 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.971 (4.20), 0.989 (9.27), 1.008(4.34), 1.989 (0.48), 2.175 (4.26), 2.445 (1.04), 2.464 (2.89), 2.483(3.04), 2.632 (16.00), 3.164 (1.17), 3.177 (1.17), 3.568 (0.57), 3.639(13.51), 4.076 (0.41), 6.145 (3.06), 7.247 (2.37), 7.269 (4.71), 7.291(2.53), 7.651 (1.99), 7.665 (2.54), 7.671 (2.38), 7.686 (1.73), 8.469(1.04), 9.364 (1.79).

Example 136-(3,5-dimethyl-1H-pyrazol-1-yl)-N-[4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]pyrimidin-4-amine

Tris(dibenzylideneacetone)dipalladium(0) (4.07 mg, 12.0 μmol) and2,2′-bis(diphenyl-phosphino)-1,1′-binaphthyl (14.9 mg, 24.0 μmol) weresuspended in toluene. Argon was poured through the solution for 10minutes. Subsequently4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (50.0 mg, 240 μmol),4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-amine (148 mg, 719 μmol) andpotassium tert-butoxylate (93.9 mg, 839 μmol) were added. The reactionmixture was stirred for 15 hours at 90° C. under microwave radiation.The mixture was diluted with saturated ammonium chloride solution andextracted three times with ethyl acetate. The combined organic phaseswere washed with brine, dried over sodium sulfate and the solvent wasremoved under reduced pressure. The crude product was purified bypreparative HPLC (method: C18, 250×30, flow 50 ml/min, Runtime: 340 min,detection at 210 nm, gradient 40% acetonitrile (6 min)→95% acetonitrile(28 min)→95% acetonitrile (38 min)→34% acetonitrile (39 min),water+0.05% formic acid) to afford 7.20 mg (8% yield) of the desiredproduct.

LC-MS (method 10): R_(t)=2.00 min; MS (ESIpos): m/z=378 [M+H]⁺

¹H-NMR (500 MHz, DMSO-d₆) δ [ppm]: 1.000 (3.97), 1.015 (8.40), 1.030(4.01), 2.073 (2.18), 2.166 (15.65), 2.516 (1.85), 2.561 (1.05), 2.626(16.00), 6.122 (3.25), 7.342 (1.32), 7.360 (2.38), 7.377 (1.47), 7.401(1.30), 7.595 (1.49), 7.606 (2.00), 7.622 (1.44), 8.451 (2.16), 9.321(1.73), 12.819 (1.70).

Example 14N-[4-chloro-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A solution of 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (44.8mg, 215 μmol) and 4-chloro-3-(4-fluorophenyl)-1H-pyrazol-5-amine (50.0mg, 236 μmol) in 1-methoxy-2-propanol (2.5 mL) was treated withhydrochloric acid in 1,4-dioxane (160 μL, 4.0 M, 640 μmol). The reactionmixture was stirred for 3 days at 120° C. The reaction mixture waspurified by preparative HPLC (method: column: Reprosil C18; 10 μm;125×30 mm/flow: 50 ml/min/eluent: A=water (0.1% formic acid),B=acetonitrile/gradient: 0.00-4.25 min=20% B, 4.50 min=30% B,19.00-22.50 min=100% B, 22.75-25.00 min=20% B) to yield 9.00 mg (11%yield) of the desired product.

LC-MS (method 10): R_(t)=2.06 min; MS (ESIpos): m/z=384 [M+H]⁺

¹H-NMR (500 MHz, DMSO-d₆) δ [ppm]: 2.090 (0.86), 2.186 (14.24), 2.225(0.60), 2.638 (16.00), 2.657 (0.85), 6.140 (3.93), 7.374 (1.47), 7.411(1.89), 7.868 (2.30), 8.503 (1.80), 9.516 (0.68), 13.483 (1.10).

Example 15 ethyl1-(6-{[4-cyclopropyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

4-cyclopropyl-3-(4-fluorophenyl)-1H-pyrazol-5-amine (200 mg, 921 μmol)and ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (258mg, 921 μmol) were disssolved in DMSO. Argon was poured through thereaction mixture. Subsequently phosphazen-base P(2)-Et (830 μL, 2.5mmol) and tBuBrettPhos Pd G3 (78.7 mg, 92.1 μmol) were added. Thereaction mixture was stirred at room temperature for 1 hour. Acetic acidwas added and the crude mixture was purified by preparative HPLC(method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 45 ml/min/eluent:A=water (0.1% formic acid), B=acetonitrile/gradient: 0.00-4.25 min=20%B, 4.50 min=70% B, 15.50 min=85% B, 16.00-23.00 min=100% B, 23.00-27.00min=20% B) to yield 84.5 mg (18% yield) of the desired product.

LC-MS (method 11): R_(t)=1.50 min; MS (ESIpos): m/z=462 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (1.95), 0.008 (1.83), 0.240(1.93), 0.725 (1.94), 0.742 (1.99), 1.091 (0.62), 1.288 (5.41), 1.298(1.94), 1.306 (11.36), 1.316 (3.17), 1.324 (5.64), 1.334 (1.45), 1.664(0.70), 1.671 (0.79), 1.684 (1.22), 1.697 (0.74), 1.704 (0.64), 2.372(14.60), 2.419 (4.59), 2.524 (1.27), 2.900 (16.00), 2.951 (4.60), 4.227(1.61), 4.245 (5.07), 4.263 (5.12), 4.281 (1.74), 4.285 (1.56), 4.303(0.41), 7.330 (1.08), 7.350 (1.77), 7.372 (1.29), 7.797 (1.54), 8.001(0.81), 8.538 (2.26), 9.016 (0.74), 9.386 (1.18), 12.887 (1.40).

Example 16 ethyl3,5-dimethyl-1-{6-[(4-methyl-5-phenyl-1H-pyrazol-3-yl)amino]pyrimidin-4-yl}-1H-pyrazole-4-carboxylate

A solution of ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (147mg, 525 μmol) and 4-methyl-5-phenyl-1H-pyrazol-3-amine (100 mg, 577μmol) in NMP (6.0 mL) was treated with hydrochloric acid in 1,4-dioxane(390 μL, 1.6 mmol). The reaction mixture was stirred for 2 hours at 190°C. under microwave radiation. After cooling to room temperature themixture was diluted with water and acetonitrile and purified bypreparative HPLC to afford 42 mg (19% yield) of the final product.

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.009 (2.19), 0.007 (1.74), 1.287(4.64), 1.305 (10.03), 1.322 (4.74), 2.082 (9.20), 2.327 (0.42), 2.370(12.85), 2.669 (0.40), 2.895 (16.00), 4.226 (1.45), 4.244 (4.38), 4.262(4.36), 4.279 (1.46), 4.576 (0.41), 7.381 (0.65), 7.399 (1.79), 7.418(1.34), 7.486 (2.20), 7.505 (3.78), 7.524 (2.02), 7.601 (3.55), 7.618(2.60), 8.544 (2.88), 9.617 (2.61).

Example 176-(3,5-dimethyl-1H-pyrazol-1-yl)-N-[5-(4-fluorophenyl)-4-methyl-1H-pyrazol-3-yl]pyrimidin-4-amine

A solution of 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (50.0mg, 240 μmol) and 5-(4-fluorophenyl)-4-methyl-1H-pyrazol-3-amine (137mg, 719 μmol) in 2-propanol (700 μL) was treated with concentratedaqueous hydrochloric acid (60 μl, 12 M, 720 μmol). The reaction mixturewas stirred for 1 hour at 100° C. under microwave radiation and for 10hours at 130° C. under microwave radiation. After cooling to roomtemperature the mixture was purified by preparative HPLC (method: C18,250×30, flow 50 ml/min, Runtime: 340 min, detection at 210 nm, eluent:A=water (0.05% formic acid), B=acetonitrile, gradient 40% B/60% A (6min)→95% B/5% A (28 min)→95% B/5% A (38 min)→34% B/76% A (39 min)) toafford 15.9 mg (18% yield) of the desired product.

LC-MS (method 10): R_(t)=1.91 min; MS (ESIpos): m/z=364 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (0.99), 0.008 (0.92), 2.058(14.37), 2.073 (1.08), 2.172 (16.00), 2.626 (14.22), 2.627 (14.44),6.127 (3.62), 7.331 (0.87), 7.351 (1.53), 7.372 (0.93), 7.646 (1.49),8.461 (2.36), 9.388 (0.82).

Example 18N-[4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]-6-(4,5,6,7-tetrahydro-2H-indazol-2-yl)pyrimidin-4-amine

The desired product was obtained out of the regioisomeric separation inthe synthesis described ofN-[4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]-6-(4,5,6,7-tetrahydro-1H-indazol-1-yl)pyrimidin-4-aminein 6% yield (7.8 mg).

LC-MS (method 10): Rt=2.12 min; MS (ESIpos): m/z=404 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.150 (1.61), −0.008 (14.95), 0.008(14.25), 0.146 (1.54), 0.991 (7.41), 1.009 (16.00), 1.028 (7.76), 1.091(1.12), 1.233 (1.54), 1.352 (0.91), 1.693 (4.05), 1.753 (3.84), 2.327(3.49), 2.366 (2.31), 2.614 (4.54), 2.630 (7.55), 2.669 (3.91), 2.709(2.79), 7.340 (4.05), 7.362 (8.87), 7.384 (6.08), 7.592 (4.61), 7.606(5.45), 7.614 (4.89), 7.627 (4.12), 8.245 (9.85), 8.424 (6.29), 9.382(5.73), 12.838 (4.89).

Example 19N-[4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]-6-(3-methyl-1H-indazol-1-yl)pyrimidin-4-amine

A solution of6-chloro-N-[4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]pyrimidin-4-amine(100 mg, 315 μmol) and 3-methyl-1H-indazole (83.2 mg, 629 μmol) in DMF(2.0 mL) was treated with caesium carbonate (308 mg, 944 μmol). Thereaction mixture was stirred at 160° C. overnight. After cooling to roomtemperature the mixture was purified by preparative HPLC (method:Column: Reprosil C18; 10 μm; 125×30 mm/Flow: 50 ml/min/Eluent: A=water(0.01% formic acid), B=acetonitrile/gradient: 0.00-5.00 min=10% B, 6.50min=20% B, 17.0-19.75 min=100% B, 19.75-23.00 min=90% B) to afford 43.3mg (30% yield) of the desired product.

LC-MS (method 10): R_(t)=2.25 min; MS (ESIpos): m/z=414 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (2.97), 0.006 (1.39), 0.008(2.01), 1.013 (3.39), 1.032 (7.03), 1.051 (3.45), 1.098 (0.41), 1.234(0.82), 2.074 (2.92), 2.519 (2.63), 2.524 (2.48), 2.560 (4.03), 2.573(16.00), 2.596 (1.33), 2.620 (1.51), 2.666 (0.46), 2.670 (0.51), 2.675(0.43), 2.731 (0.52), 2.891 (0.51), 3.004 (0.91), 5.755 (0.48), 7.287(0.49), 7.316 (1.37), 7.334 (2.38), 7.351 (2.71), 7.372 (3.65), 7.394(1.98), 7.522 (1.73), 7.553 (1.39), 7.572 (2.08), 7.592 (1.38), 7.609(2.28), 7.622 (2.51), 7.630 (2.19), 7.644 (1.76), 7.831 (2.22), 7.851(2.04), 8.557 (2.44), 8.756 (2.13), 8.777 (1.98), 9.326 (2.74), 12.846(2.13).

Example 206-(5,6-dihydrocyclopenta[c]pyrazol-2(4H)-yl)-N-[4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]pyrimidin-4-amine

The desired product was obtained out of the regioisomeric separation inthe synthesis of6-(5,6-dihydrocyclopenta[c]pyrazol-1(4H)-yl)-N-[4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]pyrimidin-4-aminein 27% yield (98% purity).

LC-MS (method 10): Rt=2.01 min; MS (ESIpos): m/z=390 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]:1.00 (t, 3H), 2.31-2.48 (m, 3H),2.52-2.55 (m, 10H), 2.58-2.71 (m, 4H), 7.26-7.42 (m, 3H), 7.60 (dd, 2H),8.16 (s, 1H), 8.41 (s, 1H), 9.36 (s, 1H), 12.81 (s, 1H).

Example 21N-[5-(4-chlorophenyl)-4-ethyl-1H-pyrazol-3-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A solution of 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (50.0mg, 240 μmol) and 5-(4-chlorophenyl)-4-ethyl-1H-pyrazol-3-amine (159 mg,719 μmol) in 2-propanol (700 mL) was treated with concentrated, aqueoushydrochloric acid (60 μL, 12 M, 720 μmol). The reaction mixture wasstirred 1 hour at 100° C. under microwave radiation. Subsequentlyadditional 3 eq of concentrated, aqueous hydrochloric acid were addedand the mixture was treated again at 130° C. for 1 hour under microwaveradiation. After cooling to room temperature the crude mixture waspurified by preparative HPLC (method: C18, 250×30, flow 50 ml/min,Runtime: 340 min, detection at 210 nm, eluent: A=water (0.05% formicacid), B=acetonitrile, gradient 40% B/60% A (6 min)→95% B/5% A (28min)→95% B/5% A (38 min)→34% B/76% A (39 min)) to yield 13.8 mg of thedesired product (15% yield).

LC-MS (method 10): R_(t)=2.15 min; MS (ESIpos): m/z=394 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (0.62), 0.008 (0.62), 0.999(3.53), 1.017 (7.89), 1.036 (3.92), 2.073 (1.50), 2.165 (14.99), 2.367(1.01), 2.519 (2.56), 2.524 (2.87), 2.561 (3.53), 2.580 (1.19), 2.625(15.21), 2.690 (0.62), 2.711 (1.01), 6.122 (3.44), 7.392 (1.94), 7.589(16.00), 8.450 (2.60), 9.334 (2.78), 12.889 (2.38).

Example 22N-[4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]-6-(4,5,6,7-tetrahydro-1H-indazol-1-yl)pyrimidin-4-amine

A solution of6-chloro-N-[4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]pyrimidin-4-amine(100 mg, 315 μmol) and 4,5,6,7-tetrahydro-1H-indazole (192 mg, 1.57mmol) in NMP (2.5 mL) was treated with DBU (140 μL, 940 μmol). Thereaction mixture was stirred overnight at 190° C. After cooling to roomtemperature the crude product was purified by preparative HPLC (method2) to yield 3.7 mg (3% yield) of the desired product.

LC-MS (method 10): R_(t)=2.21 min; MS (ESIpos): m/z=404 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 1.00 (t, 13H), 1.23 (s, 2H), 1.46 (brd, 2H), 1.64-1.71 (m, 9H), 1.71-1.80 (m, 9H), 2.36 (s, 1H), 2.45-2.48(m, 6H), 2.56-2.72 (m, 5H), 3.13 (t, 6H), 7.34 (br t, 11H), 7.53 (s,5H), 7.61 (br s, 8H), 8.13 (s, 1H), 8.24 (s, 1H), 8.40-8.49 (m, 4H),9.34 (br s, 4H), 12.74-12.92 (m, 4H).

Example 233-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-5-(4-fluorophenyl)-1-methyl-1H-pyrazole-4-carbonitrile

4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (57.9 mg, 277 μmol)and 3-amino-5-(4-fluorophenyl)-1-methyl-1H-pyrazole-4-carbonitrile (60.0mg, 277 μmol) were solved in DMSO (3.6 mL). Argon was poured through thereaction mixture. Subsequently phosphazen-base P(2)-Et (230 μl, 690μmol) and tBuBrettPhos Pd G3 (23.7 mg, 27.7 μmol) were added. Thereaction mixture was stirred at room temperature overnight. Acetic acidwas added and the crude mixture was purified by preparative HPLC(method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 45 ml/min/eluent:A=water (0.1% formic acid), B=acetonitrile/gradient: 0.00-4.25 min=20%B, 4.50 min=70% B, 15.50 min=85% B, 16.00-23.00 min=100% B, 23.00-27.00min=20% B) to yield 10.0 mg (9% yield) of the desired product.

LC-MS (method 10): R_(t)=1.94 min; MS (ESIpos): m/z=389 [M+H]⁺

¹H-NMR (500 MHz, DMSO-d₆) δ [ppm]: 1.360 (0.43), 2.212 (14.33), 2.644(11.90), 3.805 (16.00), 3.969 (0.75), 6.162 (3.49), 7.469 (2.51), 7.476(3.29), 7.482 (1.68), 7.487 (4.56), 7.500 (1.00), 7.505 (2.40), 7.734(2.34), 7.738 (1.20), 7.745 (2.61), 7.752 (2.37), 7.758 (1.07), 7.762(2.04), 8.539 (3.82), 8.540 (3.84), 10.212 (3.40).

Example 245-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-3-(4-fluorophenyl)-1-methyl-1H-pyrazole-4-carbonitrile

4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (74.3 mg, 356 μmol)and 5-amino-3-(4-fluorophenyl)-1-methyl-1H-pyrazole-4-carbonitrile (77.0mg, 356 μmol) were solved in DMSO (4.6 mL). Argon was poured through thereaction mixture. Subsequently phosphazen-base P(2)-Et (300 μl, 890μmol) and tBuBrettPhos Pd G3 (30.4 mg, 35.6 μmol) were added. Thereaction mixture was stirred at room temperature for overnight. Aceticacid was added and the crude mixture was purified by preparative HPLC(method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 45 ml/min/eluent:A=water (0.1% formic acid), B=acetonitrile/gradient: 0.00-4.25 min=20%B, 4.50 min=70% B, 15.50 min=85% B, 16.00-23.00 min=100% B, 23.00-27.00min=20% B) to yield 90.0 mg (65% yield) of the desired product.

LC-MS (method 10): R_(t)=2.04 min; MS (ESIpos): m/z=389 [M+H]⁺

¹H-NMR (600 MHz, DMSO-d₆) δ [ppm]: 2.22 (s, 3H), 2.66 (s, 3H), 3.37 (s,1H), 3.79 (s, 3H), 6.19 (s, 1H), 7.32 (s, 1H), 7.39 (t, 2H), 7.93 (t,2H), 8.59 (s, 1H), 10.30 (s, 1H).

Example 251-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,4-dimethyl-1H-pyrazol-5-ol

A solution ofN-[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-hydrazinylpyrimidin-4-amine(65.0 mg, 199 μmol) in methanol (2.0 mL) was treated with methyl2-methyl-3-oxobutanoate (23 μl, 200 μmol) (23 μL, 200 μmol). Thereaction mixture was stirred for 3 hours at 80° C. After cooling to roomtemperature the crude reaction mixture was purified by preparative HPLC(method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 50 ml/min/eluent:A=water (0.01% formic acid), B=acetonitrile/gradient: 0.00-5.00 min=10%B, 6.50 min=20% B, 17.0-19.75 min=100% B, 19.75.-23.00 min=90% B) toyield 34.8 mg of the desired product (43% yield).

LC-MS (method 9): R_(t)=0.96 min; MS (ESIpos): m/z=408 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.88 (t, 3H), 1.70 (s, 3H), 2.11 (s,3H), 2.30 (q, 2H), 3.65 (s, 3H), 7.32-7.42 (m, 2H), 7.44-7.55 (m, 2H),7.73 (br s, 1H), 8.40 (s, 1H), 9.34 (br s, 1H), 10.61 (s, 1H).

Example 26 tert-butyl2-(6-{[4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-2,4,5,7-tetrahydro-6H-pyrazolo[3,4-c]pyridine-6-carboxylate

The desired product was obtained out of the regioisomeric separationduring the synthesis of tert-butyl1-(6-{[4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-1,4,6,7-tetrahydro-5H-pyrazolo[4,3-c]pyridine-5-carboxylatein 5% yield (94% purity).

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (1.52), 0.008 (1.57), 0.991(0.98), 1.010 (2.20), 1.028 (1.04), 1.073 (0.46), 1.091 (0.95), 1.108(0.49), 1.421 (16.00), 2.558 (0.75), 2.695 (0.46), 2.710 (1.04), 2.725(0.52), 3.375 (0.48), 3.392 (0.49), 3.619 (0.56), 3.634 (1.00), 3.649(0.51), 4.464 (1.24), 7.340 (0.57), 7.363 (1.20), 7.385 (0.68), 7.591(0.66), 7.605 (0.76), 7.613 (0.68), 7.627 (0.56), 8.411 (1.30), 8.455(0.87), 9.456 (0.66), 12.847 (0.66).

Example 276-(5,6-dihydrocyclopenta[c]pyrazol-1(4H)-yl)-N-[4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]pyrimidin-4-amine

A solution of6-chloro-N-[4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]pyrimidin-4-amine(100 mg, 315 μmol) and 1,4,5,6-tetrahydrocyclopenta[c]pyrazole (170 mg,1.57 mmol, CAS 2214-03-1) in NMP (2.5 mL) was treated with DBU (140 p.1,940 μmol). The reaction mixture was stirred overnight at 190° C. Aftercooling to room temperature the crude product was purified bypreparative HPLC (method 2) to yield 34.2 mg (28% yield) of the desiredproduct.

LC-MS (method 10): R_(t)=2.09 min; MS (ESIpos): m/z=390 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (2.23), 0.988 (7.16), 1.006(16.00), 1.025 (7.68), 1.045 (2.72), 1.073 (3.98), 1.091 (8.06), 1.108(4.05), 2.328 (0.60), 2.366 (0.43), 2.562 (6.29), 2.670 (0.81), 2.710(0.46), 3.086 (3.10), 3.104 (5.32), 3.121 (3.11), 3.357 (1.33), 3.375(3.87), 3.392 (3.87), 3.409 (1.28), 7.272 (0.43), 7.340 (3.26), 7.362(6.66), 7.384 (3.85), 7.432 (2.71), 7.481 (7.78), 7.588 (3.87), 7.602(4.51), 7.610 (4.21), 7.623 (3.46), 7.681 (0.42), 8.442 (5.78), 9.392(5.47), 12.811 (4.67).

Example 28N-(5-cyclohexyl-4-ethyl-1H-pyrazol-3-yl)-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A solution of 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (50.0mg, 240 μmol) and 5-cyclohexyl-4-ethyl-1H-pyrazol-3-amine (92.6 mg, 479μmol) in NMP (400 μL) was treated with concentrated aqueous hydrochloricacid (60 μL, 12 M, 720 mmol). The resulting mixture was stirred for 1hour at 200° C. in the microwave. After cooling to room temperature thecrude product was purified by preparative HPLC (method: C18, 250×30,flow 50 ml/min, Runtime: 340 min, detection at 210 nm, gradient 40%acetonitrile (6 min)→95% acetonitrile (28 min)→95% acetonitrile (38min)→34% acetonitrile (39 min), water+0.05% formic acid) to yield 15.2mg of the desired product (16% yield).

LC-MS (method 10): R_(t)=2.15 min; MS (ESIpos): m/z=366 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (1.89), 0.008 (1.83), 0.958(3.10), 0.977 (7.05), 0.995 (3.38), 1.193 (0.63), 1.224 (0.85), 1.256(0.48), 1.304 (0.52), 1.336 (1.39), 1.368 (1.40), 1.399 (0.59), 1.470(0.60), 1.494 (1.42), 1.501 (1.50), 1.525 (1.36), 1.532 (1.32), 1.555(0.52), 1.689 (0.81), 1.720 (0.78), 1.769 (2.55), 1.778 (2.49), 2.161(16.00), 2.328 (1.20), 2.348 (2.32), 2.367 (2.45), 2.386 (0.75), 2.523(1.72), 2.592 (0.76), 2.610 (15.20), 2.652 (0.55), 2.660 (0.48), 2.665(0.51), 2.669 (0.56), 2.674 (0.44), 3.507 (0.46), 6.109 (3.88), 7.432(1.28), 8.414 (3.22), 9.148 (2.67), 12.131 (2.25).

Example 292-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-4,5,6,7-tetrahydro-2H-indazol-3-ol

A solution ofN-[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-hydrazinylpyrimidin-4-amine(65.0 mg, 199 μmol) in methanol (2.0 mL) was treated with methyl2-oxocyclohexanecarboxylate (29 μl, 200 μmol). The reaction mixture asstirred for 3 hours at 80° C. After cooling to room temperature thecrude mixture was purified using preparative HPLC (method: column:Reprosil C18; 10 μm; 125×30 mm/flow: 50 ml/min/eluent: A=water (0.01%formic acid), B=acetonitrile/gradient: 0.00-5.00 min=10% B, 6.50 min=20%B, 17.00-19.75 min=100% B, 19.75-23.00 min=90% B) to afford 43.6 mg (51%yield) of the desired product.

LC-MS (method 9): R_(t)=1.02 min; MS (ESIpos): m/z=434 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.88 (t, 3H), 1.53-1.79 (m, 4H), 2.15(br s, 2H), 2.29 (q, 2H), 2.45 (br s, 1H), 3.64 (s, 3H), 7.30-7.41 (m,2H), 7.45-7.54 (m, 2H), 7.83 (br s, 1H), 8.39 (s, 1H), 9.29 (br s, 1H),10.94 (br s, 1H).

Example 302-(6-{[4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-4,5,6,7-tetrahydro-2H-indazol-3-ol

A solution ofN-[4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]-6-hydrazinylpyrimidin-4-amine(65.0 mg, 207 μmol) in methanol (2.0 mL) was treated with methyl2-oxocyclohexanecarboxylate (30 μl, 210 μmol). After cooling to roomtemperature a precipitate occurred with was collected by filtration,washed with methanol and dried to yield 31.0 mg (36% yield) of the finalcompound.

LC-MS (method 10): R_(t)=1.78 min; MS (ESIpos): m/z=420 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.008 (1.34), 0.984 (7.35), 1.003(16.00), 1.022 (7.62), 1.627 (3.51), 1.642 (4.06), 1.668 (2.73), 1.687(4.05), 1.702 (3.61), 2.116 (3.21), 2.329 (0.49), 2.461 (5.07), 2.476(4.13), 3.170 (0.84), 7.349 (3.03), 7.607 (3.73), 7.828 (1.21), 8.403(1.90), 9.209 (0.67), 11.338 (1.44), 12.785 (0.77).

Example 31

N-{1-[2-(benzyloxy)ethyl]-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl}-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A solution of1-[2-(benzyloxy)ethyl]-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-amine(75.0 mg, 221 μmol) and4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (46.1 mg, 221 μmol)in 1-methoxy-2-propanol (1.0 mL) was treated with hydrochloric acid in1,4-dioxane (170 μl, 4.0 M, 660 μmol). The reaction vessel was cappedand the mixture was shaken overnight at 120° C. After cooling to roomtemperature the resulting mixture was purified by preparative HPLC(method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 50 ml/min/eluent:A=water (0.01% formic acid), B=acetonitrile/gradient: 0.00-5.00 min=10%B, 6.50 min=20% B, 17.0-19.75 min=100% B, 19.75-23.00 min=90% B) toyield 48.3 mg of the desired compound (43% yield).

LC-MS (method 9): R_(t)=1.36 min; MS (ESIpos): m/z=512 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.870 (4.15), 0.889 (9.45), 0.908(4.25), 1.238 (2.75), 1.400 (0.80), 2.140 (15.66), 2.282 (1.06), 2.301(3.16), 2.320 (3.16), 2.338 (1.04), 2.524 (1.07), 2.621 (16.00), 3.466(0.98), 3.773 (2.01), 3.786 (4.37), 3.799 (2.40), 4.056 (2.44), 4.069(4.36), 4.083 (2.07), 4.394 (11.10), 6.117 (4.19), 7.144 (3.07), 7.160(3.87), 7.215 (0.41), 7.233 (1.71), 7.240 (0.57), 7.250 (2.00), 7.264(3.81), 7.282 (3.68), 7.297 (2.90), 7.318 (5.07), 7.340 (3.04), 7.436(3.08), 7.441 (1.46), 7.450 (3.50), 7.457 (2.93), 7.471 (2.70), 7.484(1.60), 8.451 (3.78), 9.411 (3.41).

Example 32N-{1-[2-(benzyloxy)ethyl]-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl}-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

To a solution of1-[2-(benzyloxy)ethyl]-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-amine(145 mg, 427 μmol) in 1,4-dioxane (2.0 mL) sodium phenoxide (67.6 mg,583 μmol) was added and argon was poured through the mixture.Tris(dibenzylideneacetone)dipalladium(0) (4.62 mg, 5.05 μmol), Xantphos(6.74 mg, 11.7 μmol) and4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (81.0 mg, 388 μmol)were added to the mixture. The reaction vessel was capped and themixture was stirred at 80° C. for 3.5 hours. After cooling to roomtemperature the resulting mixture was separated via preparative HPLC(Column: Reprosil C18; 10 μm; 125×30 mm/Flow: 50 ml/min/Eluent: A=water(0,01% formic acid), B=acetonitrile/gradient: 0.00-5.00 min=10% B, 6.50min=20% B, 17.0-19.75 min=100% B, 19.75-23.00 min=90% B) to yield 58.4mg of the desired product (29% yield).

LC-MS (method 10): R_(t)=2.54 min; MS (ESIpos): m/z=512 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.150 (0.86), −0.008 (8.38), 0.008(7.14), 0.146 (0.92), 0.974 (4.59), 0.993 (10.22), 1.012 (4.78), 2.131(1.70), 2.248 (0.57), 2.327 (1.16), 2.366 (1.14), 2.444 (1.22), 2.463(3.19), 2.523 (4.51), 2.623 (16.00), 2.669 (1.30), 2.693 (0.46), 2.710(1.16), 3.162 (8.05), 3.175 (8.32), 3.755 (2.14), 3.769 (4.35), 3.783(2.32), 4.060 (0.95), 4.073 (2.59), 4.087 (2.59), 4.100 (1.30), 4.130(2.00), 4.407 (6.22), 6.130 (2.22), 7.170 (2.41), 7.209 (5.32), 7.254(3.03), 7.277 (5.68), 7.299 (3.03), 7.654 (2.43), 7.669 (3.00), 7.675(2.76), 7.690 (2.14), 8.432 (0.86), 9.316 (3.05).

Example 33 tert-butyl1-(6-{[4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-1,4,6,7-tetrahydro-5H-pyrazolo[4,3-c]pyridine-5-carboxylate

A solution of6-chloro-N-[4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]pyrimidin-4-amine(150 mg, 472 μmol) and tert-butyl1,4,6,7-tetrahydro-5H-pyrazolo[4,3-c]pyridine-5-carboxylate (158 mg, 708μmol, CAS 230301-11-8) in DMF (2.5 mL) was treated with caesiumcarbonate (461 mg, 1.42 mmol). The reaction mixture was stirred at 120°C. overnight and an additional night at 140° C. The mixture was dilutedwith water, three times extracted with ethyl acetate. The combinedorganic phases were washed with water and brine, dried over sodiumsulfate and the solvent was removed under reduced pressure. The crudeproduct was purified by preparative reverse phase HPLC (method: column:Reprosil C18; 10 μm; 125×30 mm/flow: 50 ml/min/eluent: A=water (0.01%formic acid), B=acetonitrile/gradient: 0.00-5.00 min=10% B, 6.50 min=20%B, 17.0-19.75 min=100% B, 19.75-23.00 min=90% B). Subsequently theobtained regioisomeric mixture was separated using (HPLC) method toyield 13.2 mg (6% yield) of the desired product.

LC-MS (method 9): R_(t)=1.18 min; MS (ESIpos): m/z=505 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: −0.008 (3.40), 0.008 (2.05), 0.988(1.10), 1.007 (2.36), 1.025 (1.06), 1.073 (0.74), 1.091 (1.48), 1.108(0.71), 1.424 (16.00), 2.328 (0.41), 2.519 (2.00), 2.524 (1.93), 3.214(0.83), 3.375 (0.71), 3.392 (0.70), 3.593 (0.62), 3.607 (1.06), 3.621(0.50), 4.382 (1.39), 7.339 (0.53), 7.361 (1.03), 7.383 (0.62), 7.586(0.61), 7.600 (0.70), 7.622 (0.53), 7.661 (1.24), 8.459 (0.81), 9.416(0.72), 12.813 (0.67).

Example 341-(6-{[4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,4-dimethyl-1H-pyrazol-5-ol

A suspension ofN-[4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]-6-hydrazinylpyrimidin-4-amine(65.0 mg, 207 μmol) in methanol (2.0 mL) was treated with methyl2-methyl-3-oxobutanoate (24 μl, 210 μmol, synthesis described e.g. inOrganic Letters 2015, 17(13), 3358-3361). The mixture was stirred 3 hat90° C. The reaction mixture was purified using preparative reverse phaseHPLC (method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 50ml/min/eluent: A=water (0.01% formic acid), B=acetonitrile/gradient:0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75 min=100% B, 19.75-23.00min=90% B) to yield 47.6 mg (58% yield) of the desired product.

LC-MS (method 10): R_(t)=1.72 min; MS (ESIpos): m/z=394 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 1.00 (br t, 3H), 1.66 (br s, 3H),2.11 (br s, 3H), 3.30-3.42 (m, 3H), 7.35 (br s, 2H), 7.53-7.96 (m, 3H),8.42 (br s, 1H), 9.02-9.83 (m, 1H), 11.38 (br s, 1H), 12.81 (br s, 1H).

Example 356-(3,5-dimethyl-1H-pyrazol-1-yl)-N-[3-ethyl-4-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]pyrimidin-4-amine

4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (100 mg, 479 μmol)and 3-ethyl-4-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-amine (263 mg, 1.20mmol, commercially available; CAS 956268-27-2) were dissolved in DMSO(3.0 mL). Argon was poured through the reaction mixture. Subsequentlyphosphazen-base P(2)-Et (430 μl, 1.3 mmol) and tBuBrettPhos Pd G3 (8.0ml, 58 μmol) were added. The reaction mixture was stirred at roomtemperature for 1 hour. Acetic acid was added and the crude mixture waspurified by preparative HPLC (method 2) to yield 55 mg (28% yield) ofthe desired product.

LC-MS (method 9): R_(t)=1.06 min; MS (ESIpos): m/z=392 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (2.01), 0.008 (1.87), 1.119(6.37), 1.138 (13.92), 1.156 (6.58), 2.172 (13.52), 2.328 (0.57), 2.366(0.46), 2.523 (1.89), 2.604 (16.00), 2.623 (4.95), 2.642 (4.63), 2.661(1.68), 2.670 (0.69), 2.710 (0.47), 3.588 (13.46), 3.613 (0.62), 6.131(3.94), 7.152 (2.68), 7.174 (6.21), 7.196 (3.87), 7.267 (3.00), 7.281(3.48), 7.288 (2.75), 7.302 (2.09), 8.424 (3.90), 9.401 (2.13).

Example 366-(3,5-dimethyl-1H-pyrazol-1-yl)-N-[3-(4-fluorophenyl)-4-(2,2,2-trifluoroethyl)-1H-pyrazol-5-yl]pyrimidin-4-amine

A solution of 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (100mg, 479 μmol) and3-(4-fluorophenyl)-4-(2,2,2-trifluoroethyl)-1H-pyrazol-5-amine (262 mg,95% purity, 959 μmol) in NMP (1.0 mL) was treated with concentratedaqueous hydrochloric acid (146 mg, 36% purity, 1.44 mmol). The resultingmixture was stirred for 1 hour at 180° C. in the microwave. Aftercooling to room temperature the crude product was purified bypreparative HPLC (method: C18, 250×30, flow 50 ml/min, Runtime: 340 min,detection at 210 nm, eluent: A=water (0.05% formic acid),B=acetonitrile, gradient 40% B/60% A (6 min)→95% B/5% A (28 min)→95%B/5% A (38 min)→34% B/76% A (39 min)) to yield 60 mg of the desiredproduct (29% yield).

LC-MS (method 11): R_(t)=1.37 min; MS (ESIpos): m/z=432 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (0.48), 2.194 (16.00), 2.638(13.48), 3.690 (0.60), 3.718 (1.38), 3.746 (1.30), 3.772 (0.46), 6.142(2.94), 7.352 (1.26), 7.374 (2.43), 7.396 (1.34), 7.635 (1.72), 7.649(2.19), 7.656 (2.12), 7.670 (1.66), 7.806 (0.71), 8.497 (2.28), 9.587(2.14), 13.094 (2.26).

Example 37 tert-butyl1-(6-{[4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate

A solution of6-chloro-N-[4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]pyrimidin-4-amine(834 mg, 2.60 mmol) and tert-butyl4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate (824 mg, 3.95 mmol,CAS 657428-42-7) in DMF (14.6 mL) was treated with caesium carbonate(2.56 g, 7.89 mmol). The mixture was stirred overnight at 120° C. Aftercooling to room temperature the crude product was purified bypreparative reverse phase HPLC (method: column: Reprosil C18; 10 μm;125×30 mm/flow: 50 ml/min/eluent: A=water (0.01% formic acid),B=acetonitrile/gradient: 0.00-5.00 min=10% B, 6.50 min=20% B,17.00-19.75 min=100% B, 19.75-23.00 min=90% B). Subsequently theremaining regioisomeric mixture was separated using (method 4) to yield145 mg (27% yield) of the desired product.

LC-MS (method 9): Rt=1.15 min; MS (ESIpos): m/z=491 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 1.01 (t, 3H), 1.46 (s, 9H), 2.54-2.60(m, 2H), 4.27-4.54 (m, 4H), 7.22-7.52 (m, 3H), 7.59-7.69 (m, 2H), 8.14(s, 1H), 8.39 (d, 1H), 8.47 (s, 1H), 9.52 (br s, 1H), 12.80 (br s, 2H).

Example 386-(3,5-dimethyl-1H-pyrazol-1-yl)-N-[5-(4-fluorophenyl)-4-(2-methoxyethyl)-1H-pyrazol-3-yl]pyrimidin-4-amine

4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (50.0 mg, 240 μmol)and 5-(4-fluorophenyl)-4-(2-methoxyethyl)-1H-pyrazol-3-amine (141 mg,599 μmol) were dissolved in DMSO (1.4 mL). Argon was poured through thereaction mixture. Subsequently phosphazen-base P(2)-Et (220 650 μmol)and tBuBrettPhos Pd G3 (20.5 mg, 24.0 μmol were added. The reactionmixture was stirred at room temperature overnight. Acetic acid was addedand the crude mixture was purified by preparative HPLC (method: C18,250×30, flow 50 ml/min, Runtime: 340 min, detection at 210 nm, eluent:A=water (0.05% formic acid), B=acetonitrile, gradient 40% B/60% A (6min)→95% B/5% A (28 min)→95% B/5% A (38 min)→34% B/76% A (39 min)) toyield 20.6 mg (21% yield) of the desired product.

LC-MS (method 9): R_(t)=1.05 min; MS (ESIpos): m/z=408 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 2.177 (16.00), 2.328 (0.65), 2.629(14.40), 2.670 (0.81), 2.736 (1.82), 2.753 (3.72), 2.770 (1.94), 3.147(0.88), 3.189 (15.54), 3.412 (2.09), 3.429 (3.92), 3.446 (1.78), 6.129(4.15), 7.340 (1.98), 7.362 (4.15), 7.384 (2.25), 7.597 (1.31), 7.619(2.56), 7.633 (2.85), 7.640 (2.53), 7.655 (2.07), 8.466 (3.86), 9.278(3.78), 12.839 (2.97).

Example 39N-[4-chloro-3-(4-ethoxyphenyl)-1H-pyrazol-5-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A solution of 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (20.0mg, 95.6 μmol) and 4-chloro-3-(4-ethoxyphenyl)-1H-pyrazol-5-amine (25.0mg, 105 μmol) in 1-methoxy-2-propanol (1.1 mL) was treated withhydrochloric acid in 1,4-dioxane (72 μl, 4.0 M, 290 μmol). The reactionvessel was capped and the mixture was shaken at 120° C. for 4 days.After cooling to room temperature the resulting mixture was purified bypreparative HPLC (method: column: Reprosil C18; 10 μm; 125×30 mm/flow:50 ml/min/eluent: A=water (0.1% formic acid), B=acetonitrile/gradient:0.00-4.25 min=20% B, 4.50 min=30% B, 19.00-22.50 min=100% B, 22.75-25.00min=20% B) to yield 3.0 mg of the desired compound (7% yield).

LC-MS (method 9): R_(t)=1.14 min; MS (ESIpos): m/z=410 [M+H]⁺

¹H-NMR (500 MHz, DMSO-d₆) δ [ppm]: 1.234 (1.09), 1.357 (14.02), 1.370(8.64), 2.074 (0.64), 2.175 (14.46), 2.291 (0.66), 2.364 (0.92), 2.631(16.00), 4.093 (5.52), 4.106 (5.41), 6.135 (4.51), 7.029 (0.85), 7.091(5.27), 7.106 (5.53), 7.340 (3.84), 7.724 (5.04), 7.739 (5.14), 8.028(0.64), 8.478 (4.16), 9.449 (3.96), 13.310 (3.49).

Example 40 ethyl1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

A solution of ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (70.0mg, 249 μmol) (116 mg, 477 μmol) and4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (60.1 mg, 274μmol) in N-methylpyrrolidone (2.8 mL) was treated with hydrochloric acidin 1,4-dioxane (190 μl, 4.0 M, 750 μmol). The reaction was stirred 30min at 190° C. under microwave radiation. After cooling to roomtemperature the resulting mixture was purified by preparative HPLC(method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 50 ml/min/eluent:A=water (0.1% formic acid), B=acetonitrile/gradient: 0.00-4.25 min=20%B, 4.50 min=30% B, 19.00-22.50 min=100% B, 22.75-25.00 min=20% B) toyield 15 mg of the desired compound (13% yield).

LC-MS (method 10): R_(t)=2.32 min; MS (ESIpos): m/z=464 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.872 (3.45), 0.890 (7.62), 0.909(3.58), 1.290 (4.34), 1.308 (9.11), 1.326 (4.47), 1.356 (0.83), 2.291(0.88), 2.309 (2.48), 2.328 (2.86), 2.346 (0.88), 2.380 (15.12), 2.670(0.44), 2.890 (16.00), 3.647 (15.83), 4.230 (1.32), 4.247 (4.15), 4.265(4.06), 4.283 (1.27), 7.357 (2.01), 7.379 (4.92), 7.401 (2.98), 7.499(2.57), 7.513 (2.93), 7.521 (2.36), 7.534 (1.92), 8.523 (3.48), 9.544(1.72).

Example 41N-[4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (100 mg,432 μmol) and sodium phenoxide (75.3 mg, 649 μmol) were dissolved indioxan (2.0 mL). The solution was degassed with argon.4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (99.2 mg, 476 μmol),tris(dibenzylideneacetone)dipalladium(0) (5.15 mg, 5.62 μmol) andXantphos (7.51 mg, 13.0 μmol) were added. The reaction mixture wasstirred at 80° C. for 3 days. The crude product was directly purified bypreparative HPLC (method: column: Reprosil C18; 10 μm; 125×30 mm/flow:45 ml/min/eluent: A=water (0.1% formic acid), B=acetonitrile/gradient:0.00-4.25 min=10% B, 4.50 min=20% B, 15.50 min=85% B, 16.00-18.50min=100% B, 18.75-22.00 min=20% B) to afford 35.7 mg of the desiredproduct (19% yield).

LC-MS (method 11): R_(t)=1.48 min; MS (ESIpos): m/z=404 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.008 (0.80), 0.137 (1.09), 0.147(2.93), 0.152 (2.85), 0.160 (2.95), 0.165 (2.43), 0.175 (0.88), 0.480(0.98), 0.490 (2.18), 0.495 (2.11), 0.501 (1.29), 0.511 (2.15), 0.516(1.91), 0.526 (0.62), 1.073 (0.56), 1.091 (1.09), 1.109 (0.54), 1.491(0.44), 1.504 (0.83), 1.512 (0.85), 1.525 (1.38), 1.533 (0.56), 1.538(0.73), 1.546 (0.66), 2.186 (15.26), 2.625 (12.50), 2.653 (0.82), 2.678(0.69), 3.375 (0.55), 3.392 (0.53), 3.662 (16.00), 6.131 (3.70), 7.250(3.90), 7.350 (2.25), 7.372 (4.51), 7.394 (2.48), 7.548 (2.64), 7.554(1.36), 7.562 (2.92), 7.570 (2.37), 7.579 (1.04), 7.584 (1.98), 8.441(3.73), 9.165 (3.54).

Example 426-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-[4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]pyrimidin-4-amine

4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (100 mg,432 μmol) and sodium phenoxide (75.3 mg, 649 μmol) were dissolved in1,4-dioxane (2.0 mL). The solution was degassed with argon.4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (116 mg,476 μmol), tris(dibenzylideneacetone)dipalladium(0) (5.15 mg, 5.62 μmol)and Xantphos (7.51 mg, 13.0 μmol) were added. The reaction mixture wasstirred at 80° C. overnight. The crude product was directly purified bypreparative HPLC (method: column: Reprosil C18; 10 μm; 125×30 mm/flow:45 ml/min/eluent: A=water (0.1% formic acid), B=acetonitrile/gradient:0.00-4.25 min=20% B, 4.50 min=70% B, 15.50 min=85% B, 16.00-23.00min=100% B, 23.00-27.00 min=20% B) to afford 90.9 mg (46% yield) of thedesired product.

LC-MS (method 11): R_(t)=1.65 min; MS (ESIpos): m/z=438 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.129 (0.79), 0.139 (2.56), 0.144(2.81), 0.153 (2.96), 0.157 (2.61), 0.167 (0.92), 0.482 (0.71), 0.492(1.91), 0.497 (1.95), 0.503 (1.16), 0.513 (2.04), 0.517 (1.92), 0.528(0.65), 1.507 (0.70), 1.515 (0.74), 1.520 (0.49), 1.528 (1.32), 1.536(0.49), 1.541 (0.71), 1.549 (0.65), 2.224 (14.96), 2.264 (1.67), 2.644(16.00), 2.669 (1.17), 2.677 (1.82), 3.663 (15.99), 7.275 (3.47), 7.351(1.98), 7.373 (4.28), 7.395 (2.46), 7.548 (2.40), 7.553 (1.12), 7.562(2.71), 7.570 (2.37), 7.579 (0.94), 7.584 (1.99), 8.479 (3.29), 9.297(3.62).

Example 43N-[4-cyclopropyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

4-cyclopropyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-amine (100 mg,432 μmol) and sodium phenoxide (75.3 mg, 649 μmol) were dissolved in1,4-dioxan. The solution was degassed with argon.4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (99.2 mg, 476 μmol),tris(dibenzylideneacetone)dipalladium(0) (5.15 mg, 5.62 μmol) andXantphos (7.51 mg, 13.0 μmol) were added. The reaction mixture wasstirred at 80° C. for 3 days. The crude product was directly purified bypreparative HPLC (method: column: Reprosil C18; 10 μm; 125×30 mm/flow:45 ml/min/eluent: A=water (0.1% formic acid), B=acetonitrile/gradient:0.00-4.25 min=20% B, 4.50 min=70% B, 15.50 min=85% B, 16.00-23.00min=100% B, 23.00-27.00 min=20% B) to afford 521 mg (27% yield) of thedesired product.

LC-MS (method 11): R_(t)=1.44 min; MS (ESIpos): m/z=404 [M+H]⁺

¹H-NMR (500 MHz, DMSO-d₆) δ [ppm]: −0.007 (1.10), 0.006 (0.81), 0.300(0.73), 0.697 (1.24), 1.077 (0.81), 1.092 (1.61), 1.106 (0.84), 1.634(0.67), 1.644 (0.92), 2.187 (1.87), 2.228 (3.59), 2.521 (0.49), 2.638(16.00), 2.662 (2.45), 2.663 (2.42), 3.324 (6.28), 3.376 (0.87), 3.390(0.85), 6.150 (2.11), 6.269 (0.60), 7.246 (2.08), 7.264 (4.20), 7.282(2.31), 7.350 (1.41), 7.382 (1.60), 7.457 (0.48), 7.463 (2.10), 7.466(2.14), 7.478 (1.36), 7.789 (1.31), 7.794 (1.10), 7.798 (1.25), 7.809(0.98), 7.813 (1.12), 7.820 (1.16), 7.897 (2.23), 7.899 (2.31), 8.469(0.45), 8.900 (0.69), 8.902 (0.69), 9.373 (0.94).

Example 44N-[4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3-methyl-1H-indazol-1-yl)pyrimidin-4-amine

To a solution of4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (100 mg,432 μmol) in 1,4-dioxane (2.0 mL) sodium phenoxide (75.3 mg, 649 μmol)was added and argon was poured through the mixture.Tris(dibenzylideneacetone)dipalladium(0) (5.15 mg, 5.62 μmol), Xantphos(7.51 mg, 13.0 μmol) and 1-(6-chloropyrimidin-4-yl)-3-methyl-1H-indazole(116 mg, 476 μmol) were added to the mixture. The reaction vessel wascapped and the mixture was stirred at 80° C. overnight. After cooling toroom temperature the resulting mixture was separated via preparativeHPLC (Column: Reprosil C18; 10 μm; 125×30 mm/Flow: 50 ml/min/Eluent:A=water (0.01% formic acid), B=acetonitrile/Gradient: 0.00-5.00 min=10%B, 6.50 min=20% B, 17.00-19.75 min=100% B, 19.75-23.00 min=90% B) toyield 29.6 mg of the desired product (16% yield).

LC-MS (method 11): R_(t)=1.61 min; MS (ESIpos): m/z=440 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.10-0.24 (m, 2H), 0.42-0.60 (m, 2H),1.55 (tt, 1H), 2.59 (s, 3H), 3.69 (s, 3H), 7.29-7.44 (m, 4H), 7.54-7.62(m, 3H), 7.85 (d, 1H), 8.55 (s, 1H), 8.76 (d, 1H), 9.16 (s, 1H).

Example 456-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-[4-cyclopropyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]pyrimidin-4-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation ofN-[4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3-methyl-1H-indazol-1-yl)pyrimidin-4-aminestarting from4-cyclopropyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-amine (100 mg,432 μmol) and4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (116 mg,476 μmol) to yield 35.0 mg of the desired product (17% yield).

LC-MS (method 11): Rt=1.60 min; MS (ESIpos): m/z=438 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (2.53), 0.008 (1.35), 0.295(0.74), 0.688 (1.08), 1.640 (0.73), 2.222 (1.83), 2.524 (0.82), 2.656(16.00), 3.626 (4.35), 7.241 (1.72), 7.263 (3.58), 7.285 (1.98), 7.899(1.42), 9.466 (0.57).

Example 46N-[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3-methyl-4,5,6,7-tetrahydro-2H-indazol-2-yl)pyrimidin-4-amine

A suspension ofN-[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-hydrazinylpyrimidin-4-amine(100 mg, 305 μmol) in methanol (3.0 mL) was treated with2-acetylcyclohexanone (40 μl, 310 μmol) and stirred overnight at 80° C.After cooling to room temperature a precipitate occurred with wascollected by filtration and washed with methanol to give some desiredproduct. The filtrate was taken to dryness, the crude residue waspurified by reverse phase HPLC (method: column: Reprosil C18; 10 μm;125×30 mm/flow: 50 ml/min/eluent: A=water (0.01% formic acid),B=acetonitrile/gradient: 0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75min=100% B, 19.75.00-23.00 min=90% B). In total 18.1 mg (12% yield) ofthe desired product were obtained.

LC-MS (method 10): Rt=2.43 min; MS (ESIpos): m/z=432 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.865 (4.05), 0.884 (8.67), 0.903(3.99), 1.234 (0.68), 1.716 (2.51), 2.124 (2.39), 2.275 (1.25), 2.294(3.37), 2.313 (3.36), 2.332 (1.84), 2.367 (1.58), 2.425 (4.39), 2.441(3.41), 2.524 (5.63), 2.558 (2.66), 2.574 (3.44), 2.588 (1.68), 2.670(0.78), 2.710 (0.66), 3.103 (0.48), 3.648 (16.00), 7.274 (3.61), 7.355(2.16), 7.377 (4.72), 7.399 (2.84), 7.500 (3.01), 7.513 (3.32), 7.521(2.74), 7.535 (2.24), 8.388 (0.66), 8.426 (3.62), 9.246 (0.65), 9.266(3.06).

Example 47N-[4-cyclopropyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]-6-(3-methyl-1H-indazol-1-yl)pyrimidin-4-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation ofN-[4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3-methyl-1H-indazol-1-yl)pyrimidin-4-aminestarting from4-cyclopropyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-amine (100 mg,432 μmol) and 1-(6-chloropyrimidin-4-yl)-3-methyl-1H-indazole (116 mg,476 μmol) to yield 20.0 mg of the desired product (10% yield).

LC-MS (method 11): Rt=1.58 min; MS (ESIpos): m/z=440 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.149 (0.60), 0.008 (3.86), 0.146(0.58), 0.335 (2.12), 0.717 (3.44), 1.631 (0.84), 1.652 (1.77), 1.665(2.79), 1.678 (1.68), 1.699 (0.66), 2.329 (0.89), 2.368 (0.54), 2.631(1.60), 2.671 (0.98), 2.711 (0.63), 3.654 (16.00), 7.251 (4.64), 7.273(9.29), 7.296 (5.11), 7.331 (3.27), 7.349 (5.90), 7.368 (3.98), 7.566(3.34), 7.585 (5.17), 7.605 (3.07), 7.845 (4.00), 7.864 (3.73), 7.920(4.13), 8.572 (1.76), 8.737 (6.19), 8.759 (5.98), 9.372 (4.32).

Example 48N-[4-chloro-3-(2,4-difluorophenyl)-1-methyl-1H-pyrazol-5-yl]-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation ofN-[4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3-methyl-1H-indazol-1-yl)pyrimidin-4-aminestarting from4-chloro-3-(2,4-difluorophenyl)-1-methyl-1H-pyrazol-5-amine (100 mg, 410μmol) and 4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine(110 mg, 451 μmol) to yield 43.4 mg of the desired product (23% yield).

LC-MS (method 11): R_(t)=1.58 min; MS (ESIpos): m/z=450 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.008 (0.67), 1.074 (0.96), 1.091(1.94), 1.109 (0.99), 2.236 (11.41), 2.656 (16.00), 3.375 (0.95), 3.392(0.95), 3.738 (13.08), 7.201 (0.66), 7.207 (0.67), 7.222 (1.24), 7.228(1.27), 7.243 (0.68), 7.249 (0.71), 7.384 (0.73), 7.390 (0.70), 7.409(1.10), 7.433 (0.75), 7.440 (0.70), 7.596 (0.70), 7.617 (1.39), 7.634(1.37), 7.655 (0.65), 8.548 (3.24), 9.797 (2.80).

Example 49N-[4-chloro-3-(2,4-difluorophenyl)-1-methyl-1H-pyrazol-5-yl]-6-(3-methyl-1H-indazol-1-yl)pyrimidin-4-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation ofN-[4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3-methyl-1H-indazol-1-yl)pyrimidin-4-aminestarting from4-chloro-3-(2,4-difluorophenyl)-1-methyl-1H-pyrazol-5-amine (100 mg, 410μmol) and 1-(6-chloropyrimidin-4-yl)-3-methyl-1H-indazole (110 mg, 451μmol) to yield 94.9 mg of the desired product (51% yield).

LC-MS (method 11): R_(t)=1.55 min; MS (ESIpos): m/z=452 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (2.39), 0.008 (1.44), 1.074(1.86), 1.091 (3.77), 1.109 (1.88), 2.525 (1.20), 2.603 (14.21), 3.357(0.66), 3.375 (1.85), 3.392 (1.80), 3.410 (0.59), 3.763 (16.00), 7.211(0.94), 7.216 (0.92), 7.232 (1.55), 7.237 (1.54), 7.253 (0.83), 7.259(0.82), 7.342 (1.38), 7.360 (2.45), 7.379 (1.62), 7.393 (0.95), 7.399(0.90), 7.419 (1.34), 7.423 (1.29), 7.443 (0.89), 7.449 (0.82), 7.575(1.34), 7.593 (2.10), 7.614 (1.99), 7.631 (1.15), 7.635 (1.64), 7.652(1.63), 7.673 (0.73), 7.856 (2.43), 7.876 (2.21), 8.613 (3.92), 8.731(2.73), 8.752 (2.54), 9.707 (4.17).

Example 50N-[4-chloro-3-(2,4-difluorophenyl)-1-methyl-1H-pyrazol-5-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation ofN-[4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3-methyl-1H-indazol-1-yl)pyrimidin-4-aminestarting from4-chloro-3-(2,4-difluorophenyl)-1-methyl-1H-pyrazol-5-amine (100 mg, 410μmol) and 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yflpyrimidine (94.2 mg,451 μmol) to yield 45.2 mg of the desired product (26% yield).

LC-MS (method 10): R_(t)=2.11 min; MS (ESIpos): m/z=416 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (1.68), 0.008 (1.44), 1.091(0.78), 2.198 (13.91), 2.524 (0.83), 2.639 (15.19), 3.375 (0.41), 3.736(16.00), 6.167 (3.99), 7.200 (0.73), 7.207 (0.76), 7.221 (1.42), 7.227(1.48), 7.242 (0.79), 7.248 (0.82), 7.383 (0.83), 7.390 (0.81), 7.409(1.25), 7.413 (1.21), 7.433 (0.85), 7.439 (0.82), 7.597 (0.80), 7.614(1.00), 7.618 (1.60), 7.635 (1.58), 7.639 (0.96), 7.656 (0.74), 8.510(3.30), 9.694 (2.56).

Example 51 ethyl1-{6-[(4-chloro-5-phenyl-1H-pyrazol-3-yflamino]pyrimidin-4-yl}-3,5-dimethyl-1H-pyrazole-4-carboxylate

In a microwave tube, 4-chloro-5-phenyl-1H-pyrazol-3-amine (75.9 mg, 392μmol) and sodium phenoxide (62.0 mg, 534 μmol) were suspended in1,4-dioxane (0.92 mL) and degassed by passing an Argon stream throughthe suspension. Tris(dibenzylidenaceton)dipalladium (4.24 mg, 4.63μmol), Xantphos (6.18 mg, 10.7 μmol) and ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (100mg, 356 μmol) were added and the reaction vessel was sealed. Thereaction mixture was heated at 80° C. overnight.

After cooling to ambient temperature, the reaction mixture was filteredand purified by preparative HPLC (method 4) to yield 3.0 mg of thedesired compound as an off-white powder (2% yield).

LC-MS (method 10): R_(t)=2.21 min; MS (ESIpos): m/z=438 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (3.14), 0.008 (2.65), 1.290(5.10), 1.308 (10.87), 1.316 (0.75), 1.326 (5.25), 2.379 (14.55), 2.419(0.55), 2.519 (1.62), 2.524 (1.22), 2.670 (0.44), 2.907 (16.00), 2.951(0.51), 4.231 (1.47), 4.249 (4.72), 4.266 (4.74), 4.284 (1.53), 7.367(1.06), 7.469 (0.97), 7.487 (0.86), 7.531 (1.31), 7.550 (1.97), 7.568(1.00), 7.805 (2.05), 7.823 (1.81), 8.574 (1.77), 9.726 (0.41), 13.487(1.28).

Example 52N-(4-chloro-1-methyl-5-phenyl-1H-pyrazol-3-yl)-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

In a microwave tube, 4-chloro-1-methyl-5-phenyl-1H-pyrazol-3-amine (109mg, 527 μmol) and sodium phenoxide (83.5 mg, 719 μmol) were suspended in1,4-dioxane (1.2 mL) and degassed by passing an Argon stream through thesuspension. Tris(dibenzylidenaceton)dipalladium (5.71 mg, 6.23 μmol),Xantphos (8.32 mg, 14.4 μmol) and4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (100 mg, 479 μmol)were added and the reaction vessel was sealed. The reaction mixture washeated at 80° C. overnight. After cooling to ambient temperature, thereaction mixture was filtered and purified by preparative HPLC (method4) to yield 85.0 mg of the desired compound as an off-white powder (47%yield).

LC-MS (method 10): R_(t)=2.16 min; MS (ESIpos): m/z=380 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (1.05), 0.008 (0.96), 2.189(13.99), 2.629 (11.87), 3.784 (16.00), 6.143 (3.13), 7.256 (3.75), 7.257(3.75), 7.526 (0.45), 7.539 (0.89), 7.545 (0.70), 7.550 (0.92), 7.555(0.99), 7.561 (1.26), 7.568 (1.03), 7.573 (1.43), 7.580 (13.50), 7.589(3.38), 7.594 (2.39), 8.471 (2.84), 8.473 (2.84), 9.516 (3.15).

Example 536-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-(4-chloro-1-methyl-5-phenyl-1H-pyrazol-3-yl)pyrimidin-4-amine

In a microwave tube, 4-chloro-1-methyl-5-phenyl-1H-pyrazol-3-amine (94.0mg, 452 μmol) and sodium phenoxide (71.6 mg, 617 μmol) were suspended in1,4-dioxane (1.1 mL) and degassed by passing an Argon stream through thesuspension. Tris(dibenzylidenaceton)dipalladium (4.90 mg, 5.35 μmol),Xantphos (7.14 mg, 12.3 μmol) and4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (100 mg,411 μmol) were added and the reaction vessel was sealed. The reactionmixture was heated at 80° C. overnight. After cooling to ambienttemperature, the reaction mixture was filtered and purified bypreparative HPLC (method 5) to yield 25.0 mg of the desired compound asan off-white powder (12% yield).

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.151 (0.18), −0.009 (1.54), 0.007(1.48), 0.145 (0.18), 2.227 (16.00), 2.327 (0.19), 2.365 (0.16), 2.523(0.63), 2.645 (14.27), 2.669 (4.76), 2.709 (0.17), 3.783 (14.77), 7.236(0.91), 7.258 (0.78), 7.272 (3.58), 7.315 (0.21), 7.333 (0.50), 7.352(0.31), 7.482 (0.71), 7.503 (0.87), 7.522 (0.58), 7.539 (0.79), 7.548(0.70), 7.555 (0.98), 7.560 (1.20), 7.565 (1.07), 7.578 (12.18), 7.586(2.90), 7.593 (1.90), 7.611 (0.32), 8.508 (2.56), 8.717 (0.75), 9.635(2.74).

Example 546-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-(4-chloro-5-phenyl-1H-pyrazol-3-yl)pyrimidin-4-amine

In a microwave tube, 4-chloro-5-phenyl-1H-pyrazol-3-amine (87.6 mg, 452μmol) and sodium phenoxide (71.6 mg, 617 μmol) were suspended in1,4-dioxane (1.1 mL) and degassed by passing an Argon stream through thesuspension. Tris(dibenzylidenaceton)dipalladium (4.90 mg, 5.35 μmol),Xantphos (7.14 mg, 12.3 μmol) and4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (100 mg,411 μmol) were added and the reaction vessel was sealed. The reactionmixture was heated at 80° C. overnight. After cooling to ambienttemperature, the reaction mixture was filtered and purified bypreparative HPLC (method 4) to yield 25.0 mg of the desired compound (4%yield).

LC-MS (method 10): R_(t)=2.35 min; MS (ESIpos): m/z=400 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.149 (0.58), −0.008 (5.45), 0.008(4.27), 0.015 (0.55), 0.146 (0.58), 2.073 (0.62), 2.217 (11.13), 2.266(13.28), 2.328 (0.60), 2.366 (0.57), 2.519 (2.56), 2.524 (1.96), 2.560(0.54), 2.653 (16.00), 2.670 (1.30), 2.679 (13.87), 2.710 (0.66), 7.364(1.52), 7.398 (0.46), 7.432 (0.52), 7.447 (0.66), 7.478 (1.30), 7.495(1.17), 7.540 (1.41), 7.559 (2.01), 7.577 (1.00), 7.797 (2.01), 7.815(1.87), 7.934 (2.01), 7.937 (1.94), 8.523 (1.45), 8.953 (1.80), 9.623(1.63), 13.483 (1.90).

Example 55N-[4-chloro-5-(2,4-difluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation ofN-[4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3-methyl-1H-indazol-1-yl)pyrimidin-4-aminestarting from4-chloro-5-(2,4-difluorophenyl)-1-methyl-1H-pyrazol-3-amine (100 mg, 410μmol) and 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (94.2 mg,451 μmol) to yield 27.0 mg of the desired product (16% yield).

LC-MS (method 11): R_(t)=1.45 min; MS (ESIpos): m/z=416 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 2.11-2.26 (m, 3H), 2.63 (s, 3H), 3.71(s, 3H), 6.14 (s, 1H), 7.26 (s, 1H), 7.34 (td, 1H), 7.55 (td, 1H), 7.69(td, 1H), 8.47 (s, 1H), 9.55 (s, 1H).

Example 56N-[4-chloro-5-(2,4-difluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation ofN-[4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3-methyl-1H-indazol-1-yl)pyrimidin-4-aminestarting from4-chloro-5-(2,4-difluorophenyl)-1-methyl-1H-pyrazol-3-amine (100 mg, 410μmol) and 4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine(110 mg, 451 μmol) to yield 42.2 mg of the desired product (23% yield).

LC-MS (method 10): R_(t)=2.46 min; MS (ESIpos): m/z=450 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 2.229 (15.92), 2.646 (16.00), 2.671(1.10), 3.711 (14.26), 7.273 (4.58), 7.314 (0.64), 7.320 (0.66), 7.335(1.36), 7.341 (1.33), 7.356 (0.74), 7.362 (0.73), 7.529 (0.76), 7.536(0.73), 7.554 (1.25), 7.559 (1.21), 7.578 (0.74), 7.584 (0.69), 7.664(0.73), 7.685 (1.42), 7.702 (1.41), 7.723 (0.66), 8.511 (4.29), 9.673(2.39).

Example 57N-[4-chloro-5-(2,4-difluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3-methyl-1H-indazol-1-yl)pyrimidin-4-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation ofN-[4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3-methyl-1H-indazol-1-yl)pyrimidin-4-aminestarting from4-chloro-5-(2,4-difluorophenyl)-1-methyl-1H-pyrazol-3-amine (100 mg, 410μmol) and 1-(6-chloropyrimidin-4-yl)-3-methyl-1H-indazole (110 mg, 451μmol) to yield 44.1 mg of the desired product (24% yield).

LC-MS (method 11): R_(t)=1.60 min; MS (ESIpos): m/z=452 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 2.598 (16.00), 3.736 (14.69), 7.327(1.76), 7.346 (3.70), 7.370 (5.57), 7.539 (0.86), 7.546 (0.82), 7.562(2.24), 7.580 (2.07), 7.598 (1.30), 7.681 (0.76), 7.702 (1.46), 7.719(1.51), 7.740 (0.66), 7.844 (2.31), 7.864 (2.12), 8.150 (1.43), 8.579(4.68), 8.742 (2.49), 8.763 (2.39), 9.558 (3.83).

Example 58[1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]methanol

A solution of ethyl1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(80.0 mg, 173 μmol) in THF (3.0 mL) was treated at 0° C. withdiisobutylaluminium hydride (950 μL, 1.0 M in THF, 950 μmol). Themixture was stirred for 1 hour at 0° C. Additional 5.5 eq ofdiisobutylaluminium hydride were added and it was stirred at roomtemperature overnight. The mixture was diluted with methanol and aqueoushydrochloric acid (1M) and extracted with ethyl acetate. The combinedorganic phases were washed with saturated sodium hydrogen carbonatesolution, brine, dried over sodium sulfate and the solvent was removedunder reduced pressure. The crude mixture was purified by preparativeHPLC (method 3) to yield 8.00 mg (11% yield) of the desired product.

LC-MS (method 10): R_(t)=1.72 min; MS (ESIpos): m/z=422 [M+H]⁺

¹H-NMR (500 MHz, DMSO-d₆) δ [ppm]: 0.875 (3.62), 0.891 (7.80), 0.905(3.61), 1.092 (0.78), 1.358 (1.84), 2.210 (14.68), 2.290 (0.92), 2.305(2.54), 2.320 (2.46), 2.335 (0.90), 2.615 (15.32), 3.377 (0.42), 3.652(16.00), 4.299 (3.11), 4.307 (3.11), 4.684 (0.72), 4.694 (1.23), 4.704(0.66), 7.328 (2.33), 7.362 (2.07), 7.366 (0.90), 7.380 (4.35), 7.397(2.48), 7.504 (2.51), 7.509 (1.24), 7.515 (2.83), 7.522 (2.32), 7.529(1.02), 7.533 (1.94), 8.446 (3.52), 9.320 (2.36).

Example 59 ethyl1-(6-{[3-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

In a microwave tube, ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (100mg, 356 μmol), 3-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-5-amine (80.4mg, 392 μmol) and sodium phenoxide (62.0 mg, 534 μmol) were suspended in1,4-dioxane (1.0 mL) and degassed by passing an Argon stream through thesuspension. Tris(dibenzylidenacetone)dipalladium (4.24 mg, 4.63 μmol)and Xantphos (6.18 mg, 10.7 μmol) were added and the reaction vessel wassealed. The reaction mixture was heated at 80° C. overnight. Aftercooling to ambient temperature, the reaction mixture was filtered andpurified by preparative HPLC (method 4) to yield 71 mg of the desiredcompound (42% yield).

LC-MS (method 10): R_(t)=2.19 min; MS (ESIpos): m/z=450 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 1.31 (t, J=7.1 Hz, 3H), 2.02 (s, 3H),2.91 (s, 3H), 3.66 (s, 3H), 4.26 (q, J=7.2 Hz, 2H), 6.4-7.7 (br s, 1H),7.22-7.33 (m, 2H), 7.71 (dd, J=8.4, 5.8 Hz, 2H), 8.55 (br s, 1H), 9.60(br s, 1H).

Example 60 ethyl1-(6-{[5-(4-fluorophenyl)-4-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

In a microwave tube, ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (100mg, 356 μmol), 5-(4-fluorophenyl)-4-methyl-1H-pyrazol-3-amine (74.9 mg,392 μmol) and sodium phenoxide (62.0 mg, 534 μmol) were suspended in1,4-dioxane (1.0 mL) and degassed by passing an Argon stream through thesuspension. Tris(dibenzylidenacetone)--dipalladium (4.24 mg, 4.63 μmol)and Xantphos (6.18 mg, 10.7 μmol) were added and the reaction vessel wassealed. The reaction mixture was heated at 80° C. overnight. Aftercooling to ambient temperature, the reaction mixture was filtered andpurified by preparative HPLC (method 4) to yield 18.5 mg of the desiredcompound as an off-white powder (12% yield).

LC-MS (method 10): R_(t)=2.07 min; MS (ESIpos): m/z=436 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 1.31 (t, J=7.1 Hz, 3H), 2.82 (s, 3H),2.37 (s, 3H), 2.89 (s, 3H), 4.25 (q, J=7.2 Hz, 2H), 7.31-7.41 (m, 2H),7.51 (br s, 1H), 7.65 (dd, J=8.7, 5.4 Hz, 2H), 8.54 (s, 1H), 9.61 (s,1H), 12.84 (s, 1H).

Example 61 ethyl1-(6-{[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

In a microwave tube, ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (100mg, 356 μmol), 5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-amine (80.4mg, 392 μmol) and sodium phenoxide (62.0 mg, 534 μmol) were suspended in1,4-dioxane (1.0 mL) and degassed by passing an Argon stream through thesuspension. Tris(dibenzylidenacetone)-dipalladium (4.24 mg, 4.63 μmol)and Xantphos (6.18 mg, 10.7 μmol) were added and the reaction vessel wassealed. The reaction mixture was heated at 80° C. overnight. Aftercooling to ambient temperature, the reaction mixture was filtered andpurified by preparative HPLC (method 4) to yield 22.0 mg of the desiredcompound as an off-white powder (14% yield).

LC-MS (method 10): R_(t)=2.23 min; MS (ESIpos): m/z=450 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 1.31 (t, J=7.1 Hz, 3H), 1.86 (s, 3H),2.38 (s, 3H), 2.89 (s, 3H), 3.69 (s, 3H), 4.26 (q, J=7.2 Hz, 2H),7.34-7.46 (m, 3H), 7.49-7.56 (m, 2H), 8.53 (s, 3H), 9.60 (s, 3H).

Example 62N-(1,4-dimethyl-5-phenyl-1H-pyrazol-3-yl)-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation ofN-[4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3-methyl-1H-indazol-1-yl)pyrimidin-4-aminestarting from 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (75.0mg, 359 μmol) and 1,4-dimethyl-5-phenyl-1H-pyrazol-3-amine (74.0 mg, 395μmol) to yield 43.9 mg of the desired product (32% yield).

LC-MS (method 9): R_(t)=1.06 min; MS (ESIpos): m/z=360 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (1.43), 0.008 (1.20), 1.073(0.71), 1.091 (1.46), 1.109 (0.71), 1.647 (0.67), 1.862 (0.41), 2.030(16.00), 2.172 (3.89), 2.631 (13.69), 3.375 (0.74), 3.392 (0.76), 3.666(11.36), 3.702 (0.51), 6.144 (3.02), 7.313 (0.68), 7.331 (1.89), 7.350(1.33), 7.368 (0.62), 7.384 (0.55), 7.397 (0.64), 7.422 (2.38), 7.441(4.01), 7.460 (2.06), 7.678 (2.97), 7.696 (2.55), 8.474 (1.06), 9.402(2.18).

Example 636-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-[1-(4-fluorophenyl)-3,5-dimethyl-1H-pyrazol-4-yl]pyrimidin-4-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation ofN-[4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3-methyl-1H-indazol-1-yl)pyrimidin-4-aminestarting from 1-(4-fluorophenyl)-3,5-dimethyl-1H-pyrazol-4-amine (100mg, 487 μmol) and4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (130 mg,536 μmol) to yield 43.9 mg of the desired product (32% yield).

LC-MS (method 11): R_(t)=1.49 min; MS (ESIpos): m/z=412 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 2.075 (16.00), 2.175 (11.07), 2.204(1.86), 2.632 (13.66), 7.335 (1.44), 7.357 (3.04), 7.379 (1.77), 7.591(1.48), 8.971 (1.09).

Example 646-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]-N-[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]pyrimidin-4-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation ofN-[4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3-methyl-1H-indazol-1-yl)pyrimidin-4-aminestarting from 4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine(81.5 mg, 372 μmol) and4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (100mg, 409 μmol) to yield 66.0 mg of the desired product (37% yield).

LC-MS (method 14): R_(t)=3.91 min; MS (ESIpos): m/z=428 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (1.66), 0.008 (1.57), 0.868(3.50), 0.887 (8.17), 0.906 (3.62), 2.291 (14.22), 2.301 (4.67), 2.323(2.52), 2.342 (0.77), 2.523 (0.88), 3.662 (16.00), 6.769 (3.74), 6.853(0.63), 7.252 (0.70), 7.273 (0.55), 7.292 (0.71), 7.343 (0.44), 7.361(2.29), 7.383 (5.78), 7.399 (1.08), 7.405 (2.81), 7.490 (0.60), 7.506(2.90), 7.511 (1.69), 7.519 (2.94), 7.528 (2.48), 7.536 (0.94), 7.541(1.93), 7.691 (1.21), 7.807 (0.52), 7.827 (2.49), 7.963 (1.07), 8.471(2.65), 8.720 (0.61), 9.541 (1.63).

Example 65N-(4-chloro-1-methyl-3-phenyl-1H-pyrazol-5-yl)-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

In a microwave tube, 4-chloro-1-methyl-3-phenyl-1H-pyrazol-5-amine (109mg, 527 μmol) and sodium phenoxide (83.5 mg, 719 μmol) were suspended in1,4-dioxane (1.2 mL) and degassed by passing an Argon stream through thesuspension. Tris(dibenzylidenaceton)dipalladium (5.71 mg, 6.23 μmol),Xantphos (8.32 mg, 14.4 μmol) and4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (100 mg, 479 μmol)were added and the reaction vessel was sealed. The reaction mixture washeated at 80° C. overnight. After cooling to ambient temperature, thereaction mixture was filtered and purified by preparative HPLC (method4) to yield 15.0 mg of the desired compound (8% yield).

LC-MS (method 10): R_(t)=2.14 min; MS (ESIpos): m/z=380 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 2.19 (s, 3H), 2.64 (s, 3H), 3.73 (s,3H), 6.16 (s, 1H), 7.07 (br s, 1H), 7.37-7.43 (m, 1H), 7.46-7.54 (m,2H), 7.83-7.89 (m, 2H), 8.50 (s, 1H), 9.68 (s, 1H).

Example 666-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]-N-[5-(4-fluorophenyl)-4-methyl-1H-pyrazol-3-yl]pyrimidin-4-amine

In a microwave tube,4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (100mg, 409 μmol), 5-(4-fluorophenyl)-4-methyl-1H-pyrazol-3-amine (86.0 mg,450 μmol) and sodium phenoxide (71.2 mg, 613 μmol) were suspended in1,4-dioxane (1.1 mL) and degassed by passing an Argon stream through thesuspension. Tris(dibenzylidenacetone)dipalladium (4.87 mg, 5.31 μmol)and Xantphos (7.10 mg, 12.3 μmol) were added and the reaction vessel wassealed. The reaction mixture was heated at 80° C. overnight. Aftercooling to ambient temperature, the reaction mixture was filtered andpurified by preparative HPLC (method 4) to yield 19.0 mg of the desiredcompound (9% yield)

LC-MS (method 10): R_(t)=2.03 min; MS (ESIpos): m/z=400 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 2.06 (s, 3H), 2.28 (s, 3H), 6.77 (s,1H), 7.32-7.41 (m, 2H), 7.49-7.56 (br s, 1H), 7.65 (dd, J=8.7, 5.3 Hz,2H), 7.83 (t, J=55.9 Hz, 1H), 8.49 (s, 1H), 9.61 (s, 1H), 12.88 (s, 1H).

Example 676-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]pyrimidin-4-amine

In a microwave tube,4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (100 mg,411 μmol), 5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-amine (92.9 mg,452 μmol) and sodium phenoxide (71.6 mg, 617 μmol) were suspended in1,4-dioxane (1.1 mL) and degassed by passing an Argon stream through thesuspension. Tris(dibenzylidenacetone)dipalladium (4.90 mg, 5.35 μmol)and Xantphos (7.14 mg, 12.3 μmol) were added and the reaction vessel wassealed. The reaction mixture was heated at 80° C. overnight. Aftercooling to ambient temperature, the reaction mixture was filtered andpurified by preparative HPLC (method 4) to yield 59.0 mg of the desiredcompound (35% yield).

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.150 (0.44), −0.009 (4.38), 0.007(3.43), 0.145 (0.48), 1.850 (12.78), 2.222 (14.83), 2.327 (0.49), 2.365(0.50), 2.523 (1.69), 2.640 (15.99), 2.670 (0.72), 2.709 (0.50), 3.687(16.00), 7.357 (1.96), 7.379 (4.44), 7.401 (3.27), 7.509 (2.56), 7.523(2.86), 7.531 (2.20), 7.545 (1.91), 8.482 (2.67), 9.503 (2.34).

Example 686-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-[3-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-5-yl]pyrimidin-4-amine

In a microwave tube,4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (100 mg,411 μmol), 3-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-5-amine (92.9 mg,452 μmol) and sodium phenoxide (71.6 mg, 617 μmol) were suspended in1,4-dioxane (1.1 mL) and degassed by passing an Argon stream through thesuspension. Tris(dibenzylidenacetone)dipalladium (4.90 mg, 5.35 μmol)and Xantphos (7.14 mg, 12.3 μmol) were added and the reaction vessel wassealed. The reaction mixture was heated at 80° C. overnight. Aftercooling to ambient temperature, the reaction mixture was filtered andpurified by preparative HPLC (method 4) to yield 58.0 mg of the desiredcompound (35% yield).

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 2.01 (s, 3H), 2.21 (br s, 3H), 2.65(s, 3H), 3.66 (s, 3H), 6.84-7.58 (br s, 1H), 7.23-7.31 (m, 2H),7.67-7.75 (m, 2H), 8.52 (s. 1H), 9.51 (s, 1H).

Example 696-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]-N-[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]pyrimidin-4-amine

In a microwave tube,4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (100mg, 409 μmol), 5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-amine (92.3mg, 450 μmol) and sodium phenoxide (71.2 mg, 613 μmol) were suspended in1,4-dioxane (1.1 mL) and degassed by passing an Argon stream through thesuspension. Tris(dibenzylidenacetone)dipalladium (4.87 mg, 5.31 μmol)and Xantphos (7.10 mg, 12.3 μmol) were added and the reaction vessel wassealed. The reaction mixture was heated at 80° C. overnight. Aftercooling to ambient temperature, the reaction mixture was filtered andpurified by preparative HPLC (method 4) to yield 53.4 mg of the desiredcompound (30% yield).

LC-MS (method 10): R_(t)=2.18 min; MS (ESIpos): m/z=414 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 1.854 (11.61), 2.294 (14.14), 3.698(16.00), 6.770 (4.07), 7.340 (0.50), 7.359 (2.09), 7.381 (5.08), 7.404(2.78), 7.436 (0.92), 7.459 (0.91), 7.516 (2.60), 7.529 (2.91), 7.537(2.25), 7.551 (1.92), 7.690 (1.18), 7.779 (0.48), 7.826 (2.57), 7.963(1.05), 8.476 (3.23), 9.592 (1.96).

Example 706-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]-N-[3-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-5-yl]pyrimidin-4-amine

Ina microwave tube,4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (100mg, 409 μmol), 5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-amine (92.3mg, 450 μmol) and sodium phenoxide (71.2 mg, 613 μmol) were suspended in1,4-dioxane (1.1 mL) and degassed by passing an Argon stream through thesuspension. Tris(dibenzylidenacetone)dipalladium (4.87 mg, 5.31 μmol)and Xantphos (7.10 mg, 12.3 μmol) were added and the reaction vessel wassealed. The reaction mixture was heated at 80° C. overnight. Aftercooling to ambient temperature, the reaction mixture was filtered andpurified by preparative HPLC (method 4) to yield 53.4 mg of the desiredcompound (30% yield).

LC-MS (method 10): R_(t)=2.13 min; MS (ESIpos): m/z=414 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 2.02 (s, 3H), 2.29 (s, 3H), 3.67 (s,3H), 6.42-7.48 (br s, 1H), 6.79 (s, 1H), 7.27 (t, J=8.9 Hz, 2H),7.68-7.76 (m, 2H), 7.82 (t, J=54.3 Hz, 1H), 8.51 (s, 1H), 9.60 (s, 1H).

Example 716-(3,5-dimethyl-1H-pyrazol-1-yl)-N-[3-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-5-yl]pyrimidin-4-amine

In a microwave tube, 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine(100 mg, 479 μmol), 3-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-5-amine(108 mg, 527 μmol) and sodium phenoxide (83.5 mg, 719 μmol) weresuspended in 1,4-dioxane (1.1 mL) and degassed by passing an Argonstream through the suspension. Tris(dibenzylidenacetone)dipalladium(5.71 mg, 6.23 μmol) and Xantphos (8.32 mg, 14.4 μmol) were added andthe reaction vessel was sealed. The reaction mixture was heated at 80°C. overnight. After cooling to ambient temperature, the reaction mixturewas filtered and purified by preparative HPLC (method 4) to yield 53.2mg of the desired compound (29% yield).

LC-MS (method 10): R_(t)=2.03 min; MS (ESIpos): m/z=378 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 2.02 (s, 3H), 2.17 (br s, 3H), 2.63(s, 3H), 3.66 (s, 3H), 6.15 (s, 1H), 6.31-7.49 (br s, 1H), 7.27 (t,J=8.9 Hz, 2H), 7.72 (dd, J=8.50, 5.7 Hz, 2H), 8.46 (s, 3H), 9.41 (s,3H).

Example 726-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-[5-(4-fluorophenyl)-4-methyl-1H-pyrazol-3-yl]pyrimidin-4-amine

In a microwave tube,4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (100 mg,411 μmol), 5-(4-fluorophenyl)-4-methyl-1H-pyrazol-3-amine (86.5 mg, 452μmol) and sodium phenoxide (71.6 mg, 617 μmol) were suspended in1,4-dioxane (1.1 mL) and degassed by passing an Argon stream through thesuspension. Tris(dibenzylidenacetone)dipalladium (4.90 mg, 5.35 μmol)and Xantphos (7.14 mg, 12.3 μmol) were added and the reaction vessel wassealed. The reaction mixture was heated at 80° C. overnight. Aftercooling to ambient temperature, the reaction mixture was filtered andpurified by preparative HPLC (method 4) to yield 8.5 mg of the desiredcompound (5% yield).

LC-MS (method 10): Rt=2.21 min; MS (ESIpos): m/z=398 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 2.06 (s, 3H), 2.21 (s, 3H), 2.65 (s,3H), 7.34-7.40 (m, 2H), 7.45-7.53 (br s, 1H), 7.61-7.67 (m, 2H), 8.48(s, 1H), 9.51 (s, 1H), 12.87 (s, 1H).

Example 736-(3,5-dimethyl-1H-pyrazol-1-yl)-N-[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]pyrimidin-4-amine

In a microwave tube, 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine(100 mg, 479 μmol), 5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-amine(108 mg, 527 μmol) and sodium phenoxide (83.5 mg, 719 μmol) weresuspended in 1,4-dioxane (1.1 mL) and degassed by passing an Argonstream through the suspension. Tris(dibenzylidenacetone)dipalladium(5.71 mg, 6.23 μmol) and Xantphos (8.32 mg, 14.4 μmol) were added andthe reaction vessel was sealed. The reaction mixture was heated at 80°C. overnight. After cooling to ambient temperature, the reaction mixturewas filtered and purified by preparative HPLC (method 4) to yield 91.0mg of the desired compound (50% yield).

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 1.848 (13.69), 2.183 (14.41), 2.327(0.54), 2.621 (12.35), 2.669 (0.56), 3.687 (16.00), 6.130 (3.47), 7.356(2.05), 7.378 (5.18), 7.400 (2.73), 7.510 (2.51), 7.524 (2.77), 7.532(2.21), 7.545 (1.85), 8.445 (3.21), 9.377 (2.85).

Example 74(±)-[syn-2,6-dimethylmorpholin-4-yl][1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]methanone(racemate)

A mixture of1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylicacid (72.6 mg, 167 μmol), cis-2,6-dimethylmorpholine hydrochloride (1:1)(50.6 mg, 333 μmol),(1-[Bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium3-oxid hexafluorophosphate) (139 mg, 367 μmol) andN,N-Diisopropylethylamine (120 μl, 700 μmol) was stirred overnight atroom temperature. The mixture was directly purified by preparative HPLC(method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 50 ml/min/eluent:A=water (0.01% formic acid), B=acetonitrile/gradient: 0.00-5.00 min=10%B, 6.50 min=20% B, 17.0-19.75 min=100% B, 19.75-23.00 min=90% B) toyield 49.8 mg (56% yield) of the desired product.

LC-MS (method 10): R_(t)=1.99 min; MS (ESIpos): m/z=533 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (4.17), 0.008 (2.94), 0.146(0.41), 0.871 (3.38), 0.890 (7.62), 0.909 (3.51), 1.073 (3.40), 1.091(5.53), 1.108 (3.43), 2.165 (5.64), 2.286 (0.76), 2.304 (2.17), 2.323(2.61), 2.366 (0.41), 2.523 (2.02), 2.670 (0.70), 2.710 (0.49), 3.357(0.82), 3.375 (2.25), 3.392 (2.26), 3.410 (0.95), 3.478 (0.89), 3.651(16.00), 7.359 (2.06), 7.381 (6.32), 7.403 (2.69), 7.499 (2.50), 7.512(2.88), 7.520 (2.17), 7.534 (1.85), 8.477 (3.59), 9.433 (2.07).

Example 75N-(1,4-dimethyl-3-phenyl-1H-pyrazol-5-yl)-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation ofN-[4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3-methyl-1H-indazol-1-yl)pyrimidin-4-aminestarting from 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (75.0mg, 359 μmol) and 1,4-dimethyl-3-phenyl-1H-pyrazol-5-amine (74.0 mg, 395μmol) to yield 54.2 mg of the desired product (42% yield).

LC-MS (method 9): R_(t)=1.07 min; MS (ESIpos): m/z=360 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (0.76), 0.008 (0.72), 1.073(0.69), 1.091 (1.39), 1.109 (0.70), 1.862 (14.01), 2.185 (14.42), 2.524(0.44), 2.624 (12.84), 3.375 (0.71), 3.392 (0.70), 3.702 (16.00), 6.131(3.36), 7.369 (2.04), 7.457 (2.93), 7.473 (4.28), 7.477 (4.30), 7.495(1.24), 7.499 (1.38), 7.532 (3.02), 7.551 (3.14), 7.568 (1.11), 8.449(3.16), 9.374 (2.92).

Example 76(±)-[1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl](2-methylpyrrolidin-1-yl)methanone

The described product was prepared in a manner analogous to thatdescribed in the preparation of(±)-[syn-2,6-dimethylmorpholin-4-yl][1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]methanonestarting from1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylicacid (77.4 mg, 178 μmol) and (±)2-methylpyrrolidine (30.3 mg, 355 μmol)to yield 60.0 mg of the desired product (67% yield).

LC-MS (method 10): R_(t)=2.02 min; MS (ESIpos): m/z=503 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (2.02), 0.008 (1.48), 0.872(3.81), 0.891 (8.62), 0.910 (3.94), 1.073 (1.54), 1.091 (3.14), 1.109(1.60), 1.227 (1.76), 1.241 (1.73), 1.564 (0.44), 1.576 (0.43), 1.873(0.48), 2.056 (0.43), 2.072 (0.46), 2.168 (6.02), 2.287 (0.81), 2.306(2.40), 2.324 (2.52), 2.343 (0.75), 2.519 (1.04), 2.524 (0.83), 2.590(8.35), 3.231 (0.43), 3.357 (0.58), 3.375 (1.59), 3.392 (1.55), 3.410(0.53), 3.653 (16.00), 7.359 (2.27), 7.364 (1.51), 7.374 (2.12), 7.381(4.90), 7.398 (0.94), 7.403 (2.73), 7.501 (2.62), 7.507 (1.12), 7.515(2.91), 7.523 (2.29), 7.531 (0.92), 7.537 (1.95), 8.473 (2.90), 9.418(2.19).

Example 776-(3,5-dimethyl-1H-pyrazol-1-yl)-N-[1-(4-fluorophenyl)-3-methyl-1H-pyrazol-4-yl]pyrimidin-4-amine

A solution of 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (100mg, 479 μmol) and 1-(4-fluorophenyl)-3-methyl-1H-pyrazol-4-amine (197mg, 93% purity, 959 μmol) in NMP (1 mL) was treated with concentratedaqueous hydrochloric acid (146 mg, 36%, 1.44 mmol). The resultingmixture was stirred for 1 hour at 180° C. in the microwave. Aftercooling to room temperature the crude product was poured into water. Theprecipitate was collected via filtration and purified by preparativeHPLC (method 3) to yield 18 mg of the desired product (10% yield).

LC-MS (method 9): R_(t)=1.09 min; MS (ESIpos): m/z=364 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 1.232 (0.51), 2.184 (8.68), 2.249(7.47), 2.634 (16.00), 6.133 (3.86), 7.295 (2.41), 7.317 (4.57), 7.338(2.57), 7.789 (2.22), 7.800 (2.46), 7.811 (2.32), 7.823 (2.02), 8.511(2.98), 8.676 (4.19), 9.183 (0.96).

Example 786-(3,5-dimethyl-1H-pyrazol-1-yl)-N-[1-(4-fluorophenyl)-3,5-dimethyl-1H-pyrazol-4-yl]pyrimidin-4-amine

A solution of 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (100mg, 479 μmol) and 1-(4-fluorophenyl)-3,5-dimethyl-1H-pyrazol-4-amine(269 mg, 73% purity, 959 μmol) in NMP (1 mL) was treated withconcentrated aqueous hydrochloric acid (146 mg, 1.44 mmol). Theresulting mixture was stirred for 1 hour at 180° C. in the microwave.After cooling to room temperature the crude product was poured intowater. The precipitate was collected via filtration and purified bypreparative HPLC (method 3) to yield 100 mg of the desired product (55%yield).

LC-MS (method 11): R_(t)=1.30 min; MS (ESIpos): m/z=378 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 2.077 (16.00), 2.179 (12.02), 2.616(13.32), 6.117 (2.33), 7.335 (1.57), 7.356 (3.32), 7.378 (1.88), 7.581(1.27), 7.593 (1.52), 8.397 (0.51), 8.858 (2.50).

Example 79 ethyl1-{6-[(4-chloro-1-methyl-3-phenyl-1H-pyrazol-5-yl)amino]pyrimidin-4-yl}-3,5-dimethyl-1H-pyrazole-4-carboxylate

In a microwave tube, ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (100mg, 356 μmol), 4-chloro-1-methyl-3-phenyl-1H-pyrazol-5-amine (81.4 mg,392 μmol) and sodium phenoxide (62.0 mg, 534 μmol) were suspended in1,4-dioxane (1.0 mL) and degassed by passing an Argon stream through thesuspension. Tris(dibenzylidenacetone)dipalladium (4.24 mg, 4.63 μmol)and Xantphos (6.18 mg, 10.7 μmol) were added and the reaction vessel wassealed. The reaction mixture was heated at 80° C. overnight. Aftercooling to ambient temperature, the reaction mixture was filtered andpurified by preparative HPLC (method 4) to yield 20.0 mg of the desiredcompound (12% yield).

LC-MS (method 10): R_(t)=2.28 min; MS (ESIpos): m/z=452 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 1.31 (t, J=7.1 Hz, 3H), 2.39 (s, 3H),2.92 (s, 3H), 3.74 (s, 3H), 4.26 (q, J=7.1 Hz, 2H), 6.89-7.31 (br s,1H), 7.37-7.43 (m, 1H), 7.45-7.52 (m, 2H), 7.83-7.88 (m, 2H), 8.58 (s,1H), 9.85 (s, 1H).

Example 806-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-(4-chloro-1-methyl-3-phenyl-1H-pyrazol-5-yl)pyrimidin-4-amine

In a microwave tube,4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (100 mg,411 μmol), 4-chloro-1-methyl-3-phenyl-1H-pyrazol-5-amine (94.0 mg, 452μmol) and sodium phenoxide (71.6 mg, 617 μmol) were suspended in1,4-dioxane (1.1 mL) and degassed by passing an Argon stream through thesuspension. Tris(dibenzylidenacetone)dipalladium (7.14 mg, 12.3 μmol)and Xantphos (7.14 mg, 12.3 μmol) were added and the reaction vessel wassealed. The reaction mixture was heated at 80° C. overnight. Aftercooling to ambient temperature, the reaction mixture was filtered andpurified by preparative HPLC (method 5) to yield 30.0 mg of the desiredcompound (18% yield).

LC-MS (method 10): R_(t)=2.45 min; MS (ESIpos): m/z=414 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 2.23 (s, 3H), 2.66 (s, 3H), 3.74 (s,3H), 6.80-7.32 (br s, 1H), 7.37-7.43 (m, 1H), 7.45-7.52 (m, 2H),7.84-7.89 (m, 2H), 8.54 (s, 1H), 9.78 (s, 1H).

Example 81 ethyl1-{6-[(4-chloro-1-methyl-5-phenyl-1H-pyrazol-3-yl)amino]pyrimidin-4-yl}-3,5-dimethyl-1H-pyrazole-4-carboxylate

In a microwave tube, ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (100mg, 356 μmol), 4-chloro-1-methyl-5-phenyl-1H-pyrazol-3-amine (81.4 mg,392 μmol) and sodium phenoxide (62.0 mg, 534 μmol) were suspended in1,4-dioxane (1.0 mL) and degassed by passing an Argon stream through thesuspension. Tris(dibenzylidenacetone)dipalladium (4.24 mg, 4.63 μmol)and Xantphos (6.18 mg, 10.7 μmol) were added and the reaction vessel wassealed. The reaction mixture was heated at 80° C. overnight. Aftercooling to ambient temperature, the reaction mixture was filtered andpurified by preparative HPLC (method 5) to yield 30.1 mg of the desiredcompound (19% yield).

LC-MS (method 10): R_(t)=2.35 min; MS (ESIpos): m/z=452 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (1.31), 0.008 (1.07), 1.292(4.31), 1.309 (9.11), 1.327 (4.41), 2.388 (16.00), 2.524 (0.56), 2.901(15.36), 2.933 (1.75), 3.783 (15.52), 4.232 (1.24), 4.250 (3.89), 4.258(0.73), 4.268 (3.85), 4.276 (0.64), 4.285 (1.19), 7.289 (0.49), 7.299(3.66), 7.312 (0.52), 7.526 (0.59), 7.540 (0.88), 7.551 (0.84), 7.556(1.10), 7.562 (1.39), 7.566 (1.28), 7.579 (13.15), 7.588 (3.24), 7.594(2.12), 8.555 (3.38), 8.765 (0.41), 9.724 (2.68).

Example 821-[3-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]ethanone

A solution of6-(3,5-dimethyl-1H-pyrazol-1-yl)-N-[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]pyrimidin-4-amine(130 mg, 332 μmol) and iron(III) chloride hexahydrate (89.8 mg, 332μmol) in pyridine (3.5 ml, 43 mmol) was treated with tertbutylhydroperoxide solution (190 μl, 70% purity, 1.3 mmol) and stirredfor 2 days at 50° C. Again, 1.0 eq iron(III) chloride hexahydrate (89.8mg, 332 μmol) and 4.0 eq tert-butylhydroperoxide were added and themixture was stirred over night at 50° C. After cooling to roomtemperature saturated EDTA solution was added and the mixture wasextracted with dichloromethane and ethyl acetate. The combined organicphases were washed with brine, filtered via a water-repellent filter andconcentrated in vacuum. The crude product was purified by preparativeHPLC (Waters Autopurificationsystem; column: Waters XBrigde C18 5μ100×30 mm; eluent A: water+0.2 Vol-% aq ammonia solution (32%), eluentB: acetonitrile; gradient: 0.00-0.50 min 40% B (25→70 mL/min), 0.51-5.50min 40-70% B (70mL/min), DAD scan: 210-400 nm) to yield the desiredproduct (6.30 mg, 5% yield).

LC-MS (method 13): R_(t)=1.38 min; MS (ESIpos): m/z=406 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆): δ [ppm]: 1.85 (s, 3H), 2.23 (s, 3H),2.61-2.70 (m, 3H), 3.60 (s, 3H), 6.19 (s, 1H), 7.41-7.53 (m, 2H),7.64-7.75 (m, 2H), 8.45 (d, 1H), 8.61 (d, 1H), 10.05 (s, 1H).

Example 83 ethyl1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-5-methyl-1H-pyrazole-3-carboxylate

4-Ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (100 mg, 456μmol) and sodium phenoxyde (79.4 mg, 684 μmol) were dissolved indioxane. The solution was degassed with argon. Then, ethyl1-(6-chloropyrimidin-4-yl)-5-methyl-1H-pyrazole-3-carboxylate (122 mg,456 μmol), tris(dibenzylideneacetone)dipalladium(0) (5.43 mg, 5.93 μmol)and Xantphos (7.92 mg, 13.7 μmol) were added. The reaction mixture wasstirred at 80° C. overnight. The reaction mixture was directly purifiedby preparative HPLC (method: column: Reprosil C18; 10 μm; 125×30mm/flow: 45 ml/min/eluent: A=water (0.1% formic acid),B=acetonitrile/gradient: 0.00-4.25 min=20% B, 4.50 min=70% B, 15.50min=85% B, 16.00-23.00 min=100% B, 23.00-27.00 min=20% B) to afford abrownish powder which was purified again using preparative HPLC(WUP-p-LC-basisch) to afford the pure desired product (29.3 mg, 13%yield) and some slightly impure material (51 mg) which was used in thenext step.

LC-MS (method 11): R_(t)=1.48 min; MS (ESIpos): m/z=450 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.878 (3.73), 0.897 (8.10), 0.916(3.85), 1.287 (4.30), 1.305 (8.80), 1.323 (4.36), 2.296 (1.00), 2.315(2.71), 2.333 (2.68), 2.351 (0.89), 2.678 (14.42), 3.653 (16.00), 4.280(1.39), 4.298 (4.15), 4.315 (4.10), 4.333 (1.33), 6.785 (3.87), 7.343(0.81), 7.357 (2.12), 7.379 (4.54), 7.400 (2.66), 7.450 (1.87), 7.462(1.55), 7.478 (0.82), 7.511 (2.64), 7.524 (3.16), 7.531 (2.62), 7.546(2.02), 7.783 (0.66), 7.795 (0.64), 7.808 (0.53), 7.814 (0.55), 7.822(0.56), 8.544 (2.94), 9.593 (1.64).

Example 846-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-(1,4-dimethyl-5-phenyl-1H-pyrazol-3-yl)pyrimidin-4-amine

The desired product was obtained in the same manner as described forethyl1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-5-methyl-1H-pyrazole-3-carboxylate starting from4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (75.0 mg,309 μmol) and 1,4-dimethyl-5-phenyl-1H-pyrazol-3-amine (63.5 mg, 339μmol) to yield 39.3 g (32% yield) of the desired product afterpurification by preparative HPLC (method: column: Reprosil C18; 10 μm;125×30 mm/flow: 45 ml/min/eluent: A=water (0.1% formic acid),B=acetonitrile/gradient: 0.00-4.25 min=20% B, 4.50 min=70% B, 15.50min=85% B, 16.00-23.00 min=100% B, 23.00-27.00 min=20% B).

LC-MS (method 10): R_(t)=2.31 min; MS (ESIpos): m/z=394 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 1.262 (0.63), 2.029 (15.61), 2.186(0.94), 2.212 (3.56), 2.624 (0.45), 2.649 (16.00), 3.668 (10.26), 3.702(0.53), 7.314 (0.70), 7.332 (1.84), 7.351 (1.31), 7.422 (2.39), 7.442(4.02), 7.460 (2.08), 7.676 (3.10), 7.695 (2.67), 8.510 (0.75), 9.507(1.53).

Example 85[1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl][3-fluoro-3-(trifluoromethyl)azetidin-1-yl]methanone

The described product was prepared in a manner analogous to thatdescribed in the preparation of(±)-[syn-2,6-dimethylmorpholin-4-yl][1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]methanonestarting from1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylicacid (76.3 mg, 175 μmol) and 3-fluoro-3-(trifluoromethyl)azetidinehydrochloride (1:1) (62.9 mg, 350 μmol, CAS 1803588-53-5) to yield 31 mgof the desired product (32% yield).

LC-MS (method 10): R_(t)=2.14 min; MS (ESIpos): m/z=561 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (1.97), 0.870 (3.38), 0.889(7.72), 0.908 (3.53), 2.252 (14.55), 2.287 (0.88), 2.305 (2.35), 2.324(2.58), 2.343 (0.75), 2.692 (14.95), 3.649 (16.00), 4.464 (3.92), 4.506(2.80), 7.359 (2.03), 7.381 (6.00), 7.403 (2.72), 7.499 (2.54), 7.512(2.82), 7.520 (2.25), 7.534 (1.86), 8.501 (3.59), 9.485 (1.74).

Example 866-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-(1,4-dimethyl-3-phenyl-1H-pyrazol-5-yl)pyrimidin-4-amine

The desired product was obtained in the same manner as described for6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-(1,4-dimethyl-5-phenyl-1H-pyrazol-3-yl)pyrimidin-4-aminestarting from4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (75.0 mg,309 μmol) and 1,4-dimethyl-3-phenyl-1H-pyrazol-5-amine (63.5 mg, 339μmol) to yield 30.1 g (25% yield)

LC-MS (method 10): R_(t)=2.36 min; MS (ESIpos): m/z=394 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (0.46), 0.008 (0.42), 1.234(0.47), 1.262 (0.45), 1.865 (12.99), 2.224 (14.72), 2.524 (0.46), 2.642(15.91), 3.702 (16.00), 5.754 (0.49), 7.404 (1.19), 7.456 (2.84), 7.467(1.13), 7.473 (4.00), 7.476 (4.28), 7.482 (2.22), 7.497 (1.23), 7.500(1.40), 7.533 (3.10), 7.551 (3.34), 7.569 (1.14), 8.485 (2.75), 9.500(2.39).

Example 87 ethyl[1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]acetate

A solution ofN-[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-hydrazinylpyrimidin-4-amine(170 mg, 519 μmol) and ethyl 3-acetyl-4-oxopentanoate (91 μl, 520 μmol)in methanol (5.1 ml, 130 mmol) was stirred at 80° C. overnight. Aftercooling to room temperature the precipitated was filtered, washed withmethanol and discarded. The filtrate was concentrated in vacuum andpurified by preparative HPLC (method: column: Reprosil C18; 10 μm;125×30 mm/flow: 50 ml/min/eluent: A=water (0.01% formic acid),B=acetonitrile/gradient: 0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75min=100% B, 19.75-23.00 min=90% B) to afford 83 mg of the desiredproduct (33% yield).

LC-MS (method 10): R_(t)=2.18 min; MS (ESIpos): m/z=478 [M+H]⁺

¹H-NMR (600 MHz, DMSO-d₆) δ [ppm]: 0.88 (t, 3H), 1.18 (t, 3H), 2.14 (s,3H), 2.30 (q, 2H), 2.56 (s, 3H), 3.47 (s, 2H), 3.65 (s, 3H), 4.07 (q,2H), 7.32 (br s, 1H), 7.36-7.42 (m, 2H), 7.46-7.54 (m, 2H), 8.44 (s,1H), 9.36 (s, 1H).

Example 886-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-[4-chloro-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]pyrimidin-4-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation of6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-(1,4-dimethyl-5-phenyl-1H-pyrazol-3-yl)pyrimidin-4-aminestarting from4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (97.9 mg,403 mmol) and 4-chloro-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-amine(100 mg, 443 μmol) to yield 110 mg of the desired product (61% yield).

LC-MS (method 10): R_(t)=2.50 min; MS (ESIpos): m/z=432 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (1.02), 0.008 (0.49), 1.074(0.45), 1.091 (0.89), 1.109 (0.45), 2.228 (9.57), 2.524 (0.71), 2.654(16.00), 2.669 (1.15), 3.375 (0.46), 3.392 (0.44), 3.729 (12.50), 7.301(2.29), 7.324 (4.47), 7.341 (0.99), 7.346 (2.32), 7.879 (2.27), 7.884(1.18), 7.892 (2.53), 7.901 (2.32), 7.909 (1.04), 7.914 (1.96), 8.537(1.96), 9.790 (3.05).

Example 896-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-[4-chloro-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]pyrimidin-4-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation of6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-(1,4-dimethyl-5-phenyl-1H-pyrazol-3-yl)pyrimidin-4-aminestarting from4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (97.9 mg,403 μmol) and 4-chloro-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine(100 mg, 443 μmol) to yield 85.5 mg of the desired product (49% yield).

LC-MS (method 10): R_(t)=2.51 min; MS (ESIneg): m/z=430 [M−H]⁻

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (0.99), 2.074 (0.83), 2.227(14.88), 2.646 (15.71), 3.773 (16.00), 7.278 (4.12), 7.409 (1.96), 7.431(4.35), 7.454 (2.46), 7.628 (2.39), 7.642 (2.63), 7.650 (2.35), 7.659(0.92), 7.664 (2.00), 8.507 (3.60), 9.645 (2.04).

Example 90N-[4-chloro-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation of6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-(1,4-dimethyl-5-phenyl-1H-pyrazol-3-yl)pyrimidin-4-aminestarting from 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (84.1mg, 403 μmol) and4-chloro-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-amine (100 mg, 443μmol) to yield 91.0 mg of the desired product (57% yield).

LC-MS (method 10): R_(t)=2.20 min; MS (ESIpos): m/z=398 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 2.190 (11.74), 2.637 (15.92), 3.728(16.00), 6.162 (4.00), 7.301 (2.37), 7.324 (4.89), 7.346 (2.64), 7.881(2.51), 7.895 (2.90), 7.902 (2.84), 7.916 (2.36), 8.500 (2.87), 9.688(4.45).

Example 91N-[4-chloro-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation of6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-(1,4-dimethyl-5-phenyl-1H-pyrazol-3-yl)pyrimidin-4-aminestarting from 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (84.1mg, 403 μmol) and4-chloro-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (100 mg, 443μmol) to yield 120 mg of the desired product (68% yield).

LC-MS (method 9): R_(t)=1.15 min; MS (ESIpos): m/z=398 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 2.189 (14.34), 2.627 (12.67), 3.772(16.00), 6.143 (3.77), 7.261 (4.40), 7.409 (1.94), 7.431 (4.27), 7.453(2.44), 7.629 (2.37), 7.643 (2.64), 7.651 (2.31), 7.665 (1.96), 8.470(4.06), 9.524 (3.45).

Example 922-[1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]ethanol

A solution of ethyl[1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]acetate(70.0 mg, 147 μmol) in dry THF (2.5 mL) was treated withdiisobutylaluminium hydride in THF (810 mL, 810 μmol, 1M) at 0° C. Themixture was stirred for 30 min at 0° C. and subsequently diluted withmethanol (1 mL) and hydrochloric acid (1M). The resulting mixture wasextracted three times with ethyl acetate. The combined organic phaseswere washed with brine, dried over sodium sulfate and the solvent wasremoved under reduced pressure. The crude product was purified bypreparative HPLC (method 7) to yield the desired product 32.0 mg (50%yield).

LC-MS (method 9): R_(t)=0.94 min; MS (ESIpos): m/z=436 [M+H]⁺

¹H-NMR (500 MHz, DMSO-d₆) δ [ppm]: 0.871 (3.45), 0.886 (7.66), 0.901(3.45), 1.356 (0.49), 2.162 (14.31), 2.285 (0.81), 2.300 (2.31), 2.315(2.23), 2.330 (0.73), 2.521 (1.83), 2.568 (14.60), 3.411 (1.04), 3.425(2.30), 3.436 (2.26), 3.450 (0.96), 3.648 (16.00), 4.621 (1.38), 4.631(3.12), 4.642 (1.31), 7.303 (2.21), 7.360 (1.98), 7.365 (0.76), 7.374(1.03), 7.378 (4.28), 7.383 (0.95), 7.392 (0.84), 7.396 (2.44), 7.501(2.41), 7.505 (1.07), 7.512 (2.67), 7.519 (2.15), 7.525 (0.89), 7.530(1.86), 8.427 (3.24), 9.282 (2.26).

Example 936-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]-N-[1-(4-fluorophenyl)-3,5-dimethyl-1H-pyrazol-4-yl]pyrimidin-4-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation of6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-(1,4-dimethyl-5-phenyl-1H-pyrazol-3-yl)pyrimidin-4-aminestarting from 1-(4-fluorophenyl)-3,5-dimethyl-1H-pyrazol-4-amine (100mg, 487 μmol) and4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (131mg, 536 μmol) to yield the desired product 85.6 mg (42% yield).

LC-MS (method 11): R_(t)=1.40 min; MS (ESIpos): m/z=414 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 2.081 (16.00), 2.182 (7.54), 2.285(1.25), 6.760 (1.87), 7.340 (1.26), 7.361 (2.56), 7.383 (1.46), 7.601(1.27), 7.687 (1.23), 7.823 (2.44), 7.959 (1.11), 9.057 (0.72).

Example 94[1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-5-methyl-1H-pyrazol-3-yl]methanol

The described product was prepared in a manner analogous to thatdescribed in the preparation of2-[1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]ethanolstarting from ethyl1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-5-methyl-1H-pyrazole-3-carboxylate(51.0 mg, 113 μmol) to yield the desired product (8.00 mg, 17% yield)after purification by preparative HPLC (method: column: Reprosil C18; 10μm; 125×30 mm/flow: 45 ml/min/eluent: A=water (0,1% formic acid),B=acetonitrile/gradient: 0.00-4.25 min=10% B, 4.50 min=20% B, 15.50min=85% B, 16.00-18.50 min=100% B, 18.75-22.00 min=20% B).

LC-MS (method 11): R_(t)=1.20 min; MS (ESIpos): m/z=408 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.869 (3.56), 0.888 (8.08), 0.907(3.66), 1.091 (0.40), 2.282 (0.91), 2.300 (2.68), 2.319 (2.64), 2.338(0.88), 2.524 (0.45), 2.652 (13.24), 2.685 (0.69), 3.650 (16.00), 4.407(5.27), 4.422 (5.44), 5.143 (1.52), 5.158 (3.03), 5.172 (1.40), 6.282(3.59), 7.341 (2.59), 7.357 (2.04), 7.379 (4.37), 7.401 (2.65), 7.500(2.67), 7.506 (1.21), 7.514 (2.89), 7.522 (2.43), 7.530 (0.95), 7.535(1.96), 8.461 (2.99), 9.365 (2.83).

Example 95N-[4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation of6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-(1,4-dimethyl-5-phenyl-1H-pyrazol-3-yl)pyrimidin-4-aminestarting from4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (100 mg,432 μmol) and4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (116mg, 476 μmol) to yield the desired product 76.2 mg (40% yield).

LC-MS (method 11): R_(t)=1.53 min; MS (ESIpos): m/z=440 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.133 (0.94), 0.144 (3.14), 0.148(3.27), 0.157 (3.54), 0.161 (3.00), 0.171 (1.06), 0.486 (0.81), 0.496(2.17), 0.499 (2.17), 0.516 (2.30), 0.531 (0.72), 1.497 (0.41), 1.510(0.83), 1.518 (0.90), 1.531 (1.53), 1.539 (0.62), 1.544 (0.84), 1.552(0.77), 2.298 (16.00), 3.318 (5.41), 6.772 (4.86), 7.294 (4.15), 7.354(2.25), 7.376 (4.85), 7.398 (2.73), 7.556 (2.79), 7.570 (3.24), 7.578(2.71), 7.592 (2.27), 7.699 (1.39), 7.835 (2.89), 7.971 (1.25), 8.475(4.38), 9.397 (4.11).

Example 96N-[4-cyclopropyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation of6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-(1,4-dimethyl-5-phenyl-1H-pyrazol-3-yl)pyrimidin-4-aminestarting from4-cyclopropyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-amine (100 mg,432 μmol) and4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (116mg, 476 μmol) to yield the desired product 57.0 mg (30% yield).

LC-MS (method 11): R_(t)=1.49 min; MS (ESIpos): m/z=440 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.293 (4.14), 0.703 (6.11), 1.074(0.51), 1.091 (1.01), 1.109 (0.52), 1.645 (3.58), 2.298 (7.65), 3.164(0.66), 3.176 (0.64), 3.375 (0.58), 3.392 (0.52), 3.632 (16.00), 6.790(7.75), 7.243 (6.27), 7.264 (11.96), 7.286 (6.81), 7.692 (4.44), 7.828(9.04), 7.902 (6.39), 7.964 (4.49), 8.494 (1.50), 9.549 (2.34).

Example 976-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-[4-ethyl-3-(4-fluorophenyl)-1-methyl-1-pyrazol-5-yl]pyrimidin-4-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation of6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-(1,4-dimethyl-5-phenyl-1H-pyrazol-3-yl)pyrimidin-4-aminestarting from 4-ethyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-amine(100 mg, 456 μmol) and4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (122 mg,502 μmol) to yield the desired product 79.7 mg (41% yield).

LC-MS (method 11): R_(t)=1.59 min; MS (ESIpos): m/z=426 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.969 (3.64), 0.988 (7.84), 1.006(3.75), 2.214 (3.11), 2.445 (0.92), 2.463 (2.44), 2.482 (2.57), 2.649(13.05), 3.316 (16.00), 7.248 (1.88), 7.269 (3.78), 7.291 (2.08), 7.651(1.69), 7.666 (2.26), 7.685 (1.53), 8.504 (0.73), 9.467 (1.07).

Example 986-(3,5-dimethyl-1H-pyrazol-1-yl)-N-{1,4-dimethyl-5-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-3-yl}pyrimidin-4-amine

4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (35.0 mg, 168 μmol)and 1,4-dimethyl-5-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-3-amine (50.0mg, 184 μmol) were dissolved in N-methylpyrrolidone (1.7 mL) andhydrochloric acid in 1,4-dioxane (210 μl, 4.0 M, 840 μmol) was added.The reaction vessel was sealed and the reaction mixture was heated to190° C. under microwave irradiation for 20 h. The crude mixture waspurified by preparative HPLC (method 3) to yield the desired product asa white powder (4.5 mg, 6% yield).

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 1.865 (13.92), 2.023 (0.20), 2.184(14.55), 2.327 (0.20), 2.366 (0.17), 2.622 (13.33), 2.669 (0.19), 2.709(0.15), 2.754 (0.43), 3.710 (16.00), 6.131 (3.58), 7.377 (2.01), 7.524(2.44), 7.545 (3.66), 7.616 (5.53), 7.638 (3.45), 8.004 (0.15), 8.025(0.14), 8.449 (3.43), 9.397 (3.15).

Example 996-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]pyrimidin-4-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation of6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-(1,4-dimethyl-5-phenyl-1H-pyrazol-3-yl)pyrimidin-4-aminestarting from 4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine(100 mg, 456 μmol) and4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (122 mg,502 μmol) to yield the desired product 86.1 mg (41% yield) afterpurification by preparative HPLC (method: column: Reprosil C18; 10 μm;125×30 mm/flow: 45 ml/min/eluent: A=water (0.1% formic acid),B=acetonitrile/gradient: 0.00-4.25 min=20% B, 4.50 min=70% B, 15.50min=85% B, 16.00-23.00 min=100% B, 23.00-27.00 min=20% B followed byKINTEX-S-E).

LC-MS (method 11): R_(t)=1.61 min; MS (ESIpos): m/z=426 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.869 (3.80), 0.888 (8.48), 0.906(3.96), 2.219 (14.98), 2.286 (1.04), 2.305 (2.98), 2.323 (2.94), 2.342(0.97), 2.641 (16.00), 3.315 (11.15), 7.358 (2.48), 7.367 (2.62), 7.380(4.79), 7.402 (2.70), 7.500 (2.67), 7.514 (3.06), 7.521 (2.60), 7.535(2.03), 8.478 (3.41), 9.453 (2.59).

Example 100N-[4-chloro-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]-6-(3-methyl-1H-indazol-1-yl)pyrimidin-4-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation of6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-(1,4-dimethyl-5-phenyl-1H-pyrazol-3-yl)pyrimidin-4-aminestarting from 1-(6-chloropyrimidin-4-yl)-3-methyl-1H-indazole (78.9 mg,322 μmol) and 4-chloro-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-amine(80.0 mg, 355 μmol) to yield the desired product 75.0 mg (52% yield).

LC-MS (method 9): R_(t)=1.26 min; MS (ESIpos): m/z=434 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 2.594 (11.62), 3.753 (16.00), 7.311(2.39), 7.333 (4.95), 7.356 (4.48), 7.376 (1.68), 7.571 (1.43), 7.592(2.14), 7.610 (1.30), 7.852 (2.32), 7.872 (2.18), 7.897 (2.46), 7.911(2.84), 7.919 (2.70), 7.933 (2.27), 8.602 (3.06), 8.730 (2.64), 8.752(2.54), 9.697 (4.13).

Example 1016-(3,5-dimethyl-1H-pyrazol-1-yl)-N-{1,4-dimethyl-5-[4-(trifluoromethyl)phenyl]-1H-pyrazol-3-yl}pyrimidin-4-amine

A microwave tube was charged withN-(1,4-dimethyl-1H-pyrazol-3-yl)-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-aminetrifluoroacetate (47.8 mg, 120 μmol), 1-bromo-4-(trifluoromethyl)benzene(34 μl, 240 μmol) and potassium acetate (24.8 mg, 253 μmol). The solidswere suspended in N,N-dimethylacetamide (500 μL) and the mixture wasdegassed by passing an argon flow through the suspension for 3 min.1,4-Bis(diphenylphosphino)butane-palladium(II) chloride (3.63 mg, 6.01μmol) was added and the reaction mixture was further degassed for 1 min.The vessel was sealed and heated at 150° C. for 16 h. After cooling toambient temperature, the reaction mixture was filtered and the filtratepurified by preparative HPLC (method 3) to yield the desired product(4.2 mg, 8% yield).

LC-MS (method 11): R_(t)=1.49 min; MS (ESIpos): m/z=428 [M+H]⁺

¹H-NMR (600 MHz, DMSO-d₆) δ [ppm]: 1.89 (s, 3H), 2.19 (s, 3H), 2.63 (s,3H), 3.74 (s, 3H), 6.14 (s, 1H), 7.39 (br s, 1H), 7.73 (d, 2H), 7.90 (d,2H), 7.915 (3.63), 8.46 (s, 1H), 9.45 (s, 1H).

Example 102N-[1-(4-fluorophenyl)-3,5-dimethyl-1H-pyrazol-4-yl]-6-(3-methyl-1H-indazol-1-yl)pyrimidin-4-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation of6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-(1,4-dimethyl-5-phenyl-1H-pyrazol-3-yl)pyrimidin-4-aminestarting from 1-(4-fluorophenyl)-3,5-dimethyl-1H-pyrazol-4-amine (100mg, 487 μmol) and 1-(6-chloropyrimidin-4-yl)-3-methyl-1H-indazole (131mg, 536 μmol) to yield the desired product 25.2 mg (12% yield) afterpurification by preparative HPLC (method: column: Reprosil C18; 10 μm;125×30 mm/flow: 45 ml/min/eluent: A=water (0.1% formic acid),B=acetonitrile/gradient: 0.00-4.25 min=20% B, 4.50 min=70% B, 15.50min=85% B, 16.00-23.00 min=100% B, 23.00-27.00 min=20% B followed bymethod 3).

LC-MS (method 11): R_(t)=1.47 min; MS (ESIpos): m/z=414 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 2.106 (16.00), 2.208 (10.65), 7.309(1.19), 7.328 (2.38), 7.347 (3.01), 7.369 (3.27), 7.391 (1.87), 7.544(1.39), 7.564 (2.16), 7.583 (1.47), 7.617 (1.80), 7.824 (1.75), 7.844(1.48), 8.506 (0.67), 8.735 (2.04), 8.756 (1.97), 8.866 (4.21).

Example 103N-[1-(4-fluorophenyl)-3,5-dimethyl-1H-pyrazol-4-yl]-6-(3-methyl-2H-indazol-2-yl)pyrimidin-4-amine

The described regioisomer was obtained by the regioisomeric separationof the reaction mixture in the preparation ofN-[1-(4-fluorophenyl)-3,5-dimethyl-1H-pyrazol-4-yl]-6-(3-methyl-1H-indazol-1-yl)pyrimidin-4-amine.The starting material thereof contained some of the regioisomericproduct. 9.30 mg of the depicted product were obtained.

LC-MS (method 11): Rt=1.38 min; MS (ESIpos): m/z=414 [M+H]⁺

¹H-NMR (500 MHz, DMSO-d₆) δ [ppm]: −0.007 (0.47), 1.229 (0.54), 2.079(0.54), 2.084 (0.65), 2.114 (16.00), 2.161 (0.43), 2.209 (8.30), 2.996(10.54), 7.038 (0.68), 7.280 (0.49), 7.308 (0.64), 7.348 (1.78), 7.366(3.24), 7.383 (1.88), 7.613 (1.20), 7.748 (0.72), 7.764 (0.73), 9.133(0.85).

Example 104[1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3-methyl-1H-pyrazol-5-yl]methanol

A solution of ethyl1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate(90.0 mg, 200 μmol) in THF (4.0 ml) was treated with diisobutylaluminiumhydride in THF (1.0 ml, 1.0 M, 1.0 mmol) at 0° C. The reaction mixturewas stirred at 0° C. for 30 min. Methanol (1 mL) and aqueoushydrochloric acid (0.5 M, 1 mL) were added and the mixture was extractedwith ethyl acetate. The combined organic phases were washed withsaturated sodium hydrogen carbonate solution, dried over sodium sulfateand the solvent was removed under vacuum. The crude product was purifiedby preparative HPLC (method 7) to yield 11.5 mg (14% yield).

LC-MS (method 11): R_(t)=1.28 min; MS (ESIpos): m/z=408 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.869 (3.72), 0.888 (8.29), 0.906(3.90), 1.091 (0.50), 2.218 (14.77), 2.282 (1.03), 2.301 (2.95), 2.320(2.90), 2.338 (0.99), 3.659 (16.00), 4.844 (4.16), 4.859 (4.32), 5.448(1.14), 5.464 (2.32), 5.479 (1.05), 6.315 (4.43), 7.333 (2.86), 7.359(1.92), 7.381 (4.37), 7.403 (2.66), 7.504 (2.54), 7.518 (2.93), 7.525(2.67), 7.539 (2.04), 8.444 (3.66), 9.402 (2.99).

Example 105[1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl](piperidin-1-yl)methanone

The described product was prepared in a manner analogous to thatdescribed in the preparation of(±)-[syn-2,6-dimethylmorpholin-4-yl][1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]methanone(racemate) starting from1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylic acid (76.8 mg, 176μmol) and piperidine (35 μl, 350 μmol) to yield the desired product 58.6mg (66% yield).

LC-MS (method 10): R_(t)=2.08 min; MS (ESIpos): m/z=503 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (3.08), 0.008 (1.38), 0.872(3.59), 0.891 (7.71), 0.909 (3.47), 1.074 (1.35), 1.091 (2.71), 1.109(1.35), 1.474 (1.22), 1.600 (1.68), 2.159 (14.51), 2.287 (0.95), 2.305(2.45), 2.324 (2.49), 2.343 (0.72), 2.579 (15.31), 3.357 (0.85), 3.375(1.63), 3.392 (1.54), 3.410 (0.62), 3.572 (0.65), 3.652 (16.00), 7.359(2.58), 7.371 (2.67), 7.381 (4.82), 7.403 (2.65), 7.500 (2.76), 7.506(1.35), 7.514 (3.01), 7.522 (2.27), 7.536 (1.87), 8.473 (3.59), 9.427(2.19).

Example 106[1-ent-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl](2-methylpyrrolidin-1-yl)methanone

A sample of racemic [1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methy1-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl](2-methylpyrrolidin-1-yl)methanone(30 mg, 59.7 μmol) was separated using chiral HPLC (column: DaicelChiralpak IG; 250*20 mm, 5 μM, flow 15 mL/min, 40° C., eluent 50%n-heptan/50% ethanol+0.2% diethylamine) to give 14.5 mg of the firsteluting enantiomer of[1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl](2-methy1pyrrolidin-1-yl)methanone (48% yield from racemate).

LC-MS (method 10): R_(t)=2.03 min; MS (ESIpos): m/z=503 [M+H]⁺

Chiral HPLC (Daicel Chiralcel 5 μM 100×4.6 mm, Solvent: 50% n-heptan/50%ethanol 0.2% diethylamine; 40° C., 1 mL/min) R_(t)=10.1 min, >99%enantiomeric excess.

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (1.91), 0.008 (1.56), 0.872(4.07), 0.891 (8.78), 0.910 (4.05), 1.227 (1.94), 1.241 (1.97), 1.564(0.46), 1.874 (0.51), 2.071 (0.50), 2.168 (6.28), 2.287 (0.86), 2.306(2.49), 2.324 (2.64), 2.343 (0.80), 2.524 (0.85), 2.590 (8.69), 3.230(0.46), 3.653 (16.00), 7.359 (2.29), 7.374 (2.18), 7.381 (4.92), 7.403(2.74), 7.502 (2.63), 7.507 (1.12), 7.515 (2.93), 7.523 (2.31), 7.532(0.92), 7.537 (1.96), 8.473 (2.99), 9.418 (2.25).

Optical rotation: [α]=+46.1° (c=1.00, methanol, 589 nm).

Example 107[1-ent-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl](2-methylpyrrolidin-1-yl)methanone

A sample of racemic[1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl](2-methylpyrrolidin-1-yl)methanone(30 mg, 59.7 μmol) was separated using chiral HPLC (column: DaicelChiralpak IG; 250*20 mm, 5 μM, flow 15 mL/min, 40° C., eluent 50%n-heptan/50% ethanol+0.2% diethylamine) to give 15.1 mg of the secondeluting enantiomer of [1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl](2-methylpyrrolidin-1-yl)methanone(50% yield from racemat).

LC-MS (method 10): Rt=2.03 min; MS (ESIpos): m/z=503 [M+H]⁺

Chiral HPLC (Daicel Chiralcel 5 μM 100×4.6 mm, Solvent: 50% n-heptan/50%ethanol 0.2% diethylamine; 40° C., 1 mL/min) R_(t)=12.8 min, >99%enantiomeric excess.

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.871 (4.20), 0.890 (8.64), 0.908(4.03), 1.239 (2.17), 1.563 (0.51), 1.711 (0.39), 1.873 (0.56), 2.071(0.54), 2.167 (6.71), 2.286 (0.93), 2.305 (2.56), 2.323 (2.75), 2.589(8.94), 3.652 (16.00), 4.149 (0.43), 7.358 (2.44), 7.380 (4.97), 7.402(2.70), 7.500 (2.67), 7.514 (2.99), 7.522 (2.33), 7.535 (1.87), 8.472(3.61), 9.417 (2.33).

Optical rotation: [60 ]=−47.1° (c=1.00, methanol, 589 nm).

Example 1081-(6-{[4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbonitrile

The described product was prepared in a manner analogous to thatdescribed in the preparation ofN-[4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3-methyl-1H-indazol-1-yl)pyrimidin-4-aminestarting from 4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-amine (100 mg, 487μmol) and1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbonitrile (125mg, 536 μmol) to yield the desired product 39.2 mg (19% yield).

LC-MS (method 11): R_(t)=1.37 min; MS (ESIpos): m/z=403 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.996 (3.59), 1.014 (7.84), 1.033(3.78), 2.323 (12.75), 2.377 (0.66), 2.573 (0.97), 2.792 (16.00), 2.825(0.61), 7.333 (1.37), 7.355 (2.54), 7.376 (1.60), 7.487 (0.49), 7.597(1.72), 7.611 (2.23), 7.631 (1.61), 8.546 (2.12), 9.631 (1.36), 12.862(0.55).

Example 1092-[1-(6-{[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]propan-2-ol

Ethyl1-(6-{[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(24.0 mg, 53.4 μmol) was dissolved in THF and the resulting solutioncooled to 0° C. Methyl magnesiumbromide (1.0 M in THF, 210 μL, 210 μmol)was added and the reaction mixture was allowed to warm to ambienttemperature while stirring. After 90 min, excess Grignard reagent wasquenched with aq. saturated ammonium chloride solution and extractedwith ethyl acetate (3×). The combined organic extracts were washed withbrine, dried over sodium sulfate and concentrated. The residue waspurified by preparative HPLC (column: Chromatorex C18; 125*30 mm, 10 μM,flow 75 mL/min, gradient acetonitrile/water (containing 0.1%trifluoroacetic acid) 90/10 to 5/95) to yield the desired product (11.8mg, 51% yield).

LC-MS (method 11): R_(t)=1.25 min; MS (ESIpos): m/z=436 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.149 (0.49), 0.008 (4.64), 0.146(0.47), 1.471 (16.00), 1.853 (7.70), 2.276 (7.89), 2.328 (0.47), 2.670(0.47), 2.715 (8.25), 7.329 (1.02), 7.355 (1.08), 7.377 (2.40), 7.399(1.40), 7.506 (1.35), 7.519 (1.52), 7.527 (1.28), 7.541 (1.03), 8.456(2.19), 9.411 (1.58).

Example 110N-[4-chloro-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3-methyl-1H-indazol-1-yl)pyrimidin-4-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation ofN-[4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3-methyl-1H-indazol-1-yl)pyrimidin-4-aminestarting from 1-(6-chloropyrimidin-4-yl)-3-methyl-1H-indazole (78.9 mg,322 μmol) and 4-chloro-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine(80.0 mg, 355 μmol) to yield the desired product (20 mg, 14%) afterpreparative HPLC (method: column: Reprosil C18; 10 μm; 125×30 mm/flow:50 ml/min/eluent: A=water (0.1% formic acid), B=acetonitrile/gradient:0.00-4.25 min=20% B, 4.50 min=30% B, 19.00-22.50 min=100% B, 22.75-25.00min=20% B followd by method 8).

¹H-NMR (500 MHz, DMSO-d₆): δ [ppm]: 2.60 (s, 3H), 3.80 (s, 3H),7.31-7.40 (m, 2H), 7.44 (t, 2H), 7.58 (t, 1H), 7.64-7.70 (m, 2H), 7.85(d, 1H), 8.58 (s, 1H), 8.71-8.79 (m, 1H), 9.53 (s, 1H).

Example 1112-[3-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-1-yl]ethanol

N-[1-(2-{[tert-butyl(dimethyl)silyl]oxy}ethyl)-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine(50.0 mg, 93.3 μmol) was stirred in hydrochlorid acid in dioxane (4M,1.5 ml) for 1 hour at room temperature. The mixture was diluted withdichloromethane and the solvent was removed under reduced pressure. Thiswas done twice to yield the desired product 41.9 mg (quant.).

LC-MS (method 11): R_(t)=1.32 min; MS (ESIpos): m/z=422 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.876 (4.03), 0.895 (9.08), 0.913(4.21), 1.234 (0.52), 2.195 (16.00), 2.295 (1.12), 2.313 (3.33), 2.332(3.30), 2.351 (1.10), 2.632 (14.50), 3.569 (2.31), 3.716 (2.06), 3.731(4.89), 3.746 (2.67), 3.911 (2.62), 3.926 (4.59), 3.941 (1.96), 4.868(0.75), 5.756 (0.71), 6.163 (4.20), 7.354 (2.05), 7.376 (4.51), 7.398(2.64), 7.522 (2.83), 7.536 (3.86), 7.543 (4.38), 7.557 (2.69), 8.519(3.20), 9.742 (0.42).

Example 1121-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbonitrile

The described product was prepared in an analogous manner to thatdescribed in the preparation ofN-[4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3-methyl-1H-indazol-1-yl)pyrimidin-4-aminestarting from 4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine(100 mg, 456 μmol) and1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbonitrile (147mg, 80% purity, 502 μmol) to yield 38.1 mg (20% yield) of the desiredproduct after purification by preparative HPLC (method: column: ReprosilC18; 10 μm; 125×30 mm/flow: 45 ml/min/eluent: A=water (0.1% formicacid), B=acetonitrile/gradient: 0.00-4.25 min=20% B, 4.50 min=70% B,15.50 min=85% B, 16.00-23.00 min=100% B, 23.00.-27.00 min=20% B followedby method 3).

LC-MS (method 11): R_(t)=1.45 min; MS (ESIneg): m/z=415 [M−H]⁻

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.868 (3.76), 0.887 (7.82), 0.906(3.61), 2.289 (1.22), 2.307 (2.93), 2.336 (14.26), 2.787 (14.61), 3.651(16.00), 7.342 (0.56), 7.359 (2.04), 7.381 (4.53), 7.402 (2.74), 7.421(1.45), 7.462 (0.89), 7.477 (0.64), 7.499 (2.73), 7.513 (3.06), 7.520(2.44), 7.534 (1.85), 7.781 (0.45), 7.794 (0.41), 8.147 (0.42), 8.530(3.30), 9.611 (1.43).

Example 1131-[1-(6-{[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]ethanone

Ethyl1-(6-{[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(24.0 mg, 53.4 μmol) was dissolved in THF and the resulting solution wascooled to 0° C. Methyl magnesiumbromide (1.0 M in THF, 210 μL, 210 μmol)was added and the reaction mixture allowed to warm to ambienttemperature while stirring. After 90 min, excess Grignard reagent wasquenched with saturated aqueous ammonium chloride solution and extractedwith ethyl acetate (3×). The combined organic extracts were washed withbrine, dried over sodium sulfate and concentrated. The residue waspurified by preparative HPLC (column: Chromatorex C18; 125*30 mm, 10 μM,flow 75 mL/min, gradient acetonitrile/water (containing 0.1%trifluoroacetic acid) 90/10 to 5/95) to yield desired ketone in 8% yield(1.7 mg).

LC-MS (method 11): R_(t)=1.29 min; MS (ESIpos): m/z=420 [M+H]⁺

¹H-NMR (500 MHz, DMSO-d₆) δ [ppm]: 1.86 (s, 3H), 2.45 (br d, 6H), 2.86(s, 3H), 3.68 (s, 3H), 7.25-7.45 (m, 3H), 7.48-7.58 (m, 2H), 8.54 (s,1H), 9.62 (br s, 1H).

Example 1146-(3,5-dimethyl-1H-pyrazol-1-yl)-N-[4-ethyl-5-(4-fluorophenyl)-1-(methylsulfonyl)-1H-pyrazol-3-yl]pyrimidin-4-amine

A solution of6-(3,5-dimethyl-1H-pyrazol-1-yl)-N-[4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]pyrimidin-4-amine(30.0 mg, 79.5 μmol) and triethylamine (22 μl, 160 μmol) indichloromethane (320 μl, 4.9 mmol) was treated with methanesulfonylchloride (7.4 μl, 95 μmol) and stirred overnight at room temperature.4-Dimethylaminopyridine (1.94 mg, 15.9 μmol) was added and it was stiredfor 1 hour at room temperature. Further methanesulfonyl chloride (7.4μl, 95 μmol) in acetonitrile (600 μl) was added. After 1.5 h at roomtemperature pyridine (300 μl) was added and it was stirred over night at40° C. Again, 0.6 mL acetonitrile and 0.6 mL pyridine were added and itwas stirred overnight at 40° C. After that, further 0.3 mL DMF and 5 eqof trimethylamine were added and it was stirred for 7 hours at 40° C.and over the weekend at room temperature. Potassium carbonate (33.0 mg,238 μmol) was added and the reaction mixture was stirred 6.5 h at 40°C., over night at 70° C. and 5 h at 100° C. The solvent was removedunder reduced pressure. The residue was suspended in acetonitrile/water,the precipitate was removed by filtration. The filtrate was taken todryness and purified by preparative HPLC (method: C18, 250×30, flow 50ml/min, Runtime: 340 min, detection at 210 nm, eluent: A=water (0.05%formic acid), B=acetonitrile, gradient 40% B/60% A (6 min)→95% B/5% A(28 min)→95% B/5% A (38 min)→34% B/76% A (39 min)) to yield the desiredproduct (2.30 mg, 6% yield).

LC-MS (method 9): R_(t)=1.13 min; MS (ESIpos): m/z=456 [M+H]⁺

¹H-NMR (600 MHz, DMSO-d₆) δ [ppm]: 0.897 (3.54), 0.909 (7.44), 0.922(3.62), 1.296 (0.57), 2.189 (15.25), 2.335 (0.96), 2.348 (2.87), 2.360(2.79), 2.373 (0.89), 2.639 (0.52), 2.655 (13.87), 3.477 (16.00), 3.508(0.80), 3.910 (1.07), 6.173 (4.07), 7.303 (1.93), 7.318 (4.01), 7.332(2.27), 7.511 (2.18), 7.519 (2.59), 7.525 (2.48), 7.534 (2.03), 8.087(1.51), 8.597 (4.39), 10.065 (1.32).

Example 1156-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-[1-(cyclopropylmethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]pyrimidin-4-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation ofN-[4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3-methyl-1H-indazol-1-yl)pyrimidin-4-aminestarting from1-(cyclopropylmethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-amine (105mg, 405 μmol) and4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (108 mg,445 μmol) to yield the desired product 88.5 mg (96% purity, 45% yield)after preparative HPLC (method: column: Reprosil C18; 10 μm; 125×30mm/flow: 45 ml/min/eluent: A=water (0.1% formic acid),B=acetonitrile/gradient: 0.00-4.25 min=20% B, 4.50 min=70% B, 15.50min=85% B, 16.00-23.00 min=100% B, 23.00-27.00 min=20% B followed bymethod 3).

LC-MS (method 11): R_(t)=1.70 min; MS (ESIpos): m/z=466 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.17-0.54 (m, 4H), 0.99 (t, 3H),1.14-1.28 (m, 1H), 2.20 (br s, 3H), 2.40-2.49 (m, 2H), 2.64 (s, 3H),3.80 (br d, 2H), 6.51 (br s, 1H), 7.27 (t, 2H), 7.69 (br t, 2H), 8.49(br s, 1H), 9.42 (br s, 1H).

Example 1166-(3,5-dimethyl-1H-pyrazol-1-yl)-N-{1,4-dimethyl-3-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-5-yl}pyrimidin-4-amine

A microwave vial was charged with4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (69.9 mg, 335 μmol)and 1,4-dimethyl-3-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-5-amine (100mg, 369 μmol), which were dissolved in N-methyl-2-pyrrolidone (2.6 mL)and treated with a solution of hydrochloric acid in dioxane (4 M, 0.4mL). The microwave vial was sealed and heated to 190° C. for 20 h in alaboratory microwave. After cooling to ambient temperature and removalof the volatiles under vacuum, the residue was purified by preparativeHPLC (method 3) to yield the desired product (7.6 mg, 5% yield).

LC-MS (method 10): R_(t)=2.28 min; MS (ESIpos): m/z=444 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (3.48), 0.008 (3.36), 0.146(0.42), 2.041 (16.00), 2.072 (0.98), 2.174 (4.28), 2.198 (0.92), 2.210(0.68), 2.328 (0.45), 2.366 (0.41), 2.631 (14.18), 2.670 (0.51), 2.710(0.43), 3.674 (11.50), 3.704 (1.33), 6.147 (2.94), 7.420 (3.09), 7.441(3.32), 7.804 (3.37), 7.825 (2.99), 8.473 (0.96), 9.424 (2.47).

Example 1176-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-{1,4-dimethyl-5-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-3-yl}pyrimidin-4-amine

A microwave vial was charged with4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (61.1 mg,251 μmol) and1,4-dimethyl-5-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-3-amine (75.0 mg,277 μmol), which were dissolved in NMP (2.6 mL) and treated with asolution of hydrochloric acid in dioxane (4 M, 0.3 mL). The microwavevial was sealed and heated to 190° C. for 20 h in a laboratorymicrowave. After cooling to ambient temperature and removal of thevolatiles under vacuum, the residue was purified was purified bypreparative HPLC (method 4) to yield the desired product as a whitepowder (18.7 mg, 15% yield).

LC-MS (method 10): R_(t)=2.55 min; MS (ESIpos): m/z=478 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 1.87 (s, 3H), 2.22 (s, 3H), 2.64 (s,3H), 3.71 (s, 3H), 7.39-7.45 (m, 1H), 7.51-7.56 (m, 2H), 7.60-7.65 (m,2H), 8.49 (s, 1H), 9.52 (s, 1H).

Example 1184-(3-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-1,4-dimethyl-1H-pyrazol-5-yl)benzonitrile

A microwave tube was charged withN-(1,4-dimethyl-1H-pyrazol-3-yl)-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine(100 mg, 353 μmol), 4-bromobenzonitrile (106 mg, 582 μmol) and potassiumacetate (72.7 mg, 741 μmol). The solids were suspended inN,N-dimethylacetamide (1.2 mL) and the reaction mixture was degassed bypassing an argon flow through the suspension for 3 min.1,4-Bis(diphenylphosphino)butane-palladium(II) chloride (10.7 mg, 17.6μmol) was added and the reaction mixture further degassed for 1 min. Thevessel was sealed and heated at 150° C. for 16 h. After cooling toambient temperature, the reaction mixture was filtered and the filtratepurified by preparative HPLC (column: Chromatorex C18; 125*30 mm, 10 μM,flow 75 mL/min, gradient acetonitrile/water (containing 0.1%trifluoroacetic acid) 90/10 to 5/95) to yield the desired product (13.6mg, 10% yield).

LC-MS (method 11): R_(t)=1.30 min; MS (ESIneg): m/z=383 [M−H]⁻

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.008 (1.80), 1.885 (13.27), 2.185(13.76), 2.328 (0.59), 2.366 (0.64), 2.523 (1.83), 2.623 (12.59), 2.670(0.60), 2.710 (0.58), 3.737 (16.00), 3.759 (1.19), 6.135 (3.52), 7.381(2.04), 7.699 (4.01), 7.720 (4.64), 7.818 (0.85), 8.004 (4.47), 8.024(3.96), 8.453 (3.84), 9.435 (2.84).

Example 119N-[1-cyclopropyl-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation ofN-[4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3-methyl-1H-indazol-1-yl)pyrimidin-4-aminestarting from1-cyclopropyl-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-amine (100 mg, 408μmol) and 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (93.6 mg,448 μmol) to yield 77.5 mg of the desired product (96% purity, 44%yield) after purification by preparative HPLC (method: column: ReprosilC18; 10 μm; 125×30 mm/flow: 45 ml/min/eluent: A=water (0.1% formicacid), B=acetonitrile/gradient: 0.00-4.25 min=20% B, 4.50 min=70% B,15.50 min=85% B, 16.00-23.00 min=100% B, 23.00.00-27.00 min=20% B andsubsequently method 3).

LC-MS (method 11): R_(t)=1.53 min; MS (ESIneg): m/z=416 [M−H]⁻

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (0.54), 0.008 (0.40), 0.867(2.27), 0.880 (2.21), 0.885 (2.17), 0.973 (4.23), 0.992 (9.50), 1.010(4.60), 1.040 (2.21), 1.074 (0.51), 1.091 (0.67), 2.175 (3.30), 2.436(0.96), 2.454 (2.71), 2.473 (2.73), 2.635 (16.00), 3.358 (0.44), 3.368(0.64), 3.375 (1.09), 3.386 (1.12), 3.393 (1.04), 3.403 (0.61), 6.144(2.91), 7.241 (2.52), 7.263 (5.20), 7.285 (2.86), 7.639 (1.70), 7.654(2.23), 7.660 (2.15), 7.674 (1.61), 8.471 (0.88), 9.393 (1.01).

Example 1206-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-[1-cyclopropyl-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]pyrimidin-4-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation ofN-[4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3-methyl-1H-indazol-1-yl)pyrimidin-4-aminestarting from1-cyclopropyl-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-amine (110 mg, 448μmol) and 4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine(120 mg, 493 μmol) to yield 9.40 mg (100% purity, 5% yield) of thedesired product.

LC-MS (method 11): R_(t)=1.68 min; MS (ESIpos): m/z=452 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.78-0.93 (m, 2H), 0.93-1.06 (m, 5H),2.09-2.27 (m, 3H), 2.37-2.48 (m, 2H), 2.65 (s, 3H), 3.33-3.46 (m, 1H),7.26 (t, 2H), 7.56-7.72 (m, 2H), 8.50 (br s, 1H), 9.49 (br s, 1H).

Example 121N-[1-(cyclopropylmethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation ofN-[4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3-methyl-1H-indazol-1-yl)pyrimidin-4-aminestarting from1-(cyclopropylmethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-amine (100mg, 386 μmol) and 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine(88.5 mg, 424 μmol) to yield 95.5 mg (98% purity, 56% yield) of thedesired product.

LC-MS (method 11): R_(t)=1.56 min; MS (ESIneg): m/z=430 [M−H]⁻

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.298 (2.53), 0.309 (2.69), 0.435(2.73), 0.454 (2.86), 0.977 (3.81), 0.995 (8.34), 1.014 (3.99), 1.176(0.41), 1.188 (0.76), 1.195 (0.73), 1.207 (1.11), 1.219 (0.70), 1.225(0.74), 2.171 (2.98), 2.444 (0.82), 2.463 (2.16), 2.481 (2.13), 2.630(16.00), 2.654 (0.43), 2.684 (0.45), 3.797 (2.30), 3.813 (2.29), 6.139(2.67), 7.255 (2.44), 7.277 (4.94), 7.299 (2.70), 7.676 (1.57), 7.690(2.26), 7.710 (1.54), 8.459 (0.74), 9.337 (0.64).

Example 122 methyl4-(3-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-1,4-dimethyl-1H-pyrazol-5-yl)benzoate

A microwave tube was charged withN-(1,4-dimethyl-1H-pyrazol-3-yl)-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine(100 mg, 353 μmol), methyl 4-bromobenzoate (125 mg, 582 μmol) andpotassium acetate (72.7 mg, 741 μmol). The solids were suspended inN,N-dimethylacetamide (1.2 mL) and the reaction mixture was degassed bypassing an argon flow through the suspension for 3 min.1,4-Bis(diphenylphosphino)butane-palladium(II) chloride (10.7 mg, 17.6μmol) was added and the reaction mixture further degassed for 1 min. Thevessel was sealed and heated at 150° C. for 16 h. After cooling toambient temperature, the reaction mixture was filtered and the filtratepurified by preparative HPLC (method 7) to yield the desired product(13.6 mg, 10% yield).

LC-MS (method 11): R_(t)=1.37 min; MS (ESIneg): m/z=416 [M−H]⁻

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 1.89 (s, 3H), 2.19 (s, 3H), 2.62 (s,3H), 3.74 (s, 3H), 3.90 (s, 3H), 6.13 (s, 1H), 7.37 (s, 1H), 7.65 (m,2H), 8.10 (m, 2H), 8.45 (s, 1H), 9.41 (s, 1H).

Example 123azetidin-1-yl[1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]methanone

The described product was prepared in a manner analogous to thatdescribed in the preparation of(±)-[syn-2,6-dimethylmorpholin-4-yl][1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]methanone(racemate) starting from1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylicacid (50.0 mg, 115 μmol) and azetidine (31 μl, 460 μmol) to yield 44.1mg (100% purity, 81% yield) of the desired product.

LC-MS (method 11): R_(t)=1.77 min; MS (ESIpos): m/z=475 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (1.23), 0.008 (1.04), 0.869(3.43), 0.888 (7.95), 0.907 (3.53), 1.073 (1.03), 1.091 (2.13), 1.109(1.07), 2.202 (0.53), 2.227 (15.10), 2.241 (2.09), 2.260 (1.39), 2.284(0.92), 2.303 (2.30), 2.322 (2.31), 2.340 (0.74), 2.524 (0.58), 2.656(15.60), 3.375 (1.07), 3.392 (1.04), 3.650 (16.00), 3.988 (2.05), 7.358(2.61), 7.363 (2.43), 7.374 (1.28), 7.380 (4.57), 7.397 (0.86), 7.402(2.68), 7.499 (2.55), 7.505 (1.07), 7.513 (2.83), 7.521 (2.23), 7.529(0.87), 7.535 (1.91), 8.482 (2.83), 9.443 (1.86).

Example 124(3,3-difluoroazetidin-1-yl)[1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]methanone

The described product was prepared in a manner analogous to thatdescribed in the preparation of(±)-[syn-2,6-dimethylmorpholin-4-yl][1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]methanone(racemate) starting from1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylicacid (50.0 mg, 115 μmol) and 3,3-difluoroazetidine hydrochloride (1:1)(29.7 mg, 230 μmol) to yield 44.8 mg (100% purity, 76% yield) of thedesired product.

LC-MS (method 11): R_(t)=1.94 min; MS (ESIpos): m/z=511 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (1.02), 0.008 (0.78), 0.871(3.50), 0.890 (7.96), 0.908 (3.57), 1.073 (0.63), 1.091 (1.27), 1.109(0.65), 2.261 (14.32), 2.288 (0.87), 2.306 (2.35), 2.325 (2.35), 2.344(0.75), 2.524 (0.50), 2.697 (15.46), 3.375 (0.63), 3.392 (0.63), 3.650(16.00), 4.430 (3.42), 4.462 (7.04), 4.493 (3.12), 7.359 (2.03), 7.364(0.90), 7.381 (5.93), 7.398 (1.06), 7.403 (2.73), 7.500 (2.58), 7.506(1.15), 7.513 (2.89), 7.522 (2.25), 7.530 (0.91), 7.535 (1.90), 8.499(2.69), 9.480 (1.75).

Example 1252-[1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3-methyl-1H-pyrazol-5-yl]propan-2-ol

ethyl1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate(100 mg, 222 μmol) was dissolved in THF, under argon. At 0° C.bromo(methyl)magnesium (780 μl, 1.0 M, 780 μmol) was added dropwise. Thereaction mixture was stirred at 0° C. for 2 h. Additional 3.5 eq ofmethylmagnesium bromide were added and the reaction mixture was stirredfor 2 h. Then ammonium chloride solution was used to dilute thereaction. Then, ethyl acetate was added. The aqueous layer was extractedtwice with ethyl acetate. The organic layers were combined, dried overmagnesium sulfate and concentrated under vacuum. The crude product waspurified by preparative HPLC (method: column: Reprosil C18; 10 μm;125×30 mm/flow: 45 ml/min/eluent: A=water (0.1% formic acid),B=acetonitrile/gradient: 0.00-4.25 min=20% B, 4.50 min=70% B, 15.50min=85% B, 16.00-23.00min=100% B, 23.00-27.00min=20% B) to afford 65.9mg (100% purity, 68% yield) of the desired product.

LC-MS (method 11): R_(t)=1.40 min; MS (ESIneg): m/z=434 [M−H]⁻

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.878 (2.40), 0.897 (5.40), 0.916(2.50), 1.091 (0.49), 1.478 (16.00), 2.204 (9.48), 2.297 (0.54), 2.315(1.51), 2.334 (1.51), 2.352 (0.50), 3.656 (10.93), 6.281 (3.81), 7.361(1.31), 7.383 (2.92), 7.405 (1.75), 7.441 (0.72), 7.506 (1.76), 7.520(1.99), 7.527 (1.59), 7.541 (1.29), 7.753 (3.67), 8.538 (2.05), 9.662(0.77).

Example 126[1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl](3-fluoroazetidin-1-yl)methanone

The described product was prepared in a manner analogous to thatdescribed in the preparation of(±)-[syn-2,6-dimethylmorpholin-4-yl][1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]methanone(racemate) starting from1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylicacid (50.0 mg, 115 μmol) and 3-fluoroazetidine hydrochloride (1:1) (25.6mg, 230 μmol) to yield 40.9 mg (100% purity, 72% yield) of the desiredproduct.

LC-MS (method 10): R_(t)=1.79 min; MS (ESIpos): m/z=493 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.89 (t, 3H), 2.24 (s, 3H), 2.28-2.39(m, 2H), 2.67 (s, 3H), 3.65 (s, 3H), 3.90-4.17 (m, 2H), 4.33 (br s, 2H),5.29-5.58 (m, 1H), 7.24-7.42 (m, 3H), 7.46-7.60 (m, 2H), 8.49 (s, 1H),9.46 (s, 1H).

Example 1271-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-N,N,3,5-tetramethyl-1H-pyrazole-4-carboxamide

The described product was prepared in a manner analogous to thatdescribed in the preparation of(±)-[syn-2,6-dimethylmorpholin-4-yl][1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]methanone(racemate) starting from1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylicacid (50.0 mg, 115 μmol) and N-methylmethanamine (230 μl, 2.0 M, 460μmol) to yield 40.3 mg (100% purity, 76% yield) of the desired product.

LC-MS (method 10): R_(t)=1.75 min; MS (ESIpos): m/z=463 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.89 (t, 3H), 2.16 (s, 3H), 2.31 (q,2H), 2.58 (s, 3H), 2.78-3.07 (m, 6H), 3.65 (s, 3H), 7.30-7.43 (m, 3H),7.47-7.55 (m, 2H), 8.47 (s, 1H), 9.43 (s, 1H).

Example 128[3-(difluoromethyl)pyrrolidin-1-yl][1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]methanone

The described product was prepared in a manner analogous to thatdescribed in the preparation of(±)-[syn-2,6-dimethylmorpholin-4-yl][1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]methanone(racemate) starting from1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylicacid (50.0 mg, 115 μmol) and 3-(difluoromethyl)pyrrolidine hydrochloride(1:1) (36.2 mg, 230 μmol) to yield 50.3 mg (100% purity, 81% yield) ofthe desired product.

LC-MS (method 10): R_(t)=1.89 min; MS (ESIpos): m/z=539 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 0.89 (t, 3H), 1.78-2.11 (m, 2H), 2.18(s, 3H), 2.26-2.39 (m, 2H), 2.60 (s, 3H), 2.64-2.89 (m, 1H), 3.33-3.70(m, 7H), 5.88-6.38 (m, 1H), 7.31-7.43 (m, 3H), 7.47-7.58 (m, 2H), 8.48(s, 1H), 9.43 (s, 1H).

Example 129N-[4-chloro-1-(2,2-difluoroethyl)-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation ofN-[4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3-methyl-1H-indazol-1-yl)pyrimidin-4-aminestarting from4-chloro-1-(2,2-difluoroethyl)-3-(4-fluorophenyl)-1H-pyrazol-5-amine(90.0 mg, 326 μmol) and4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (74.9 mg, 359 μmol)to yield 61.8 mg (96% purity, 41% yield) of the desired product afterpreparative HPLC (method: column: Reprosil C18; 10 μm; 125×30 mm/flow:45 ml/min/eluent: A=water (0,1% formic acid), B=acetonitril/gradient:0.00-4.25 min=20% B, 4.50 min=70% B, 15.50 min=85% B, 16.00-23.00min=100% B, 23.00-27.00 min=20% B and subsequently method 4).

LC-MS (method 11): R_(t)=1.52 min; MS (ESIneg): m/z=446 [M−H]⁻

¹H-NMR (600 MHz, DMSO-d₆) δ [ppm]: 2.19 (s, 3H), 2.60-2.66 (m, 3H),4.48-4.69 (m, 2H), 6.16 (s, 1H), 6.27-6.54 (m, 1H), 7.03-7.24 (m, 1H),7.30-7.39 (m, 2H), 7.85-7.97 (m, 2H), 8.50 (s, 1H), 9.73 (s, 1H).

Example 130N-[4-chloro-1-(2,2-difluoroethyl)-5-(4-fluorophenyl)-1H-pyrazol-3-yl]-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation ofN-[4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3-methyl-1H-indazol-1-yl)pyrimidin-4-aminestarting from4-chloro-1-(2,2-difluoroethyl)-5-(4-fluorophenyl)-1H-pyrazol-3-amine(95.0 mg, 345 μmol) and4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (92.2 mg,379 μmol) to yield 78.2 mg (98% purity, 46% yield) of the desiredproduct.

LC-MS (method 11): R_(t)=1.66 min; MS (ESIpos): m/z=482 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: 2.22 (s, 3H), 2.60-2.71 (m, 3H), 4.49(td, 2H), 6.12-6.53 (m, 1H), 7.33-7.49 (m, 3H), 7.53-7.63 (m, 2H), 8.53(s, 1H), 9.80 (s, 1H).

Example 1316-(3,5-dimethyl-1H-pyrazol-1-yl)-N-[4-ethyl-5-(4-fluoro-2-methylphenyl)-1H-pyrazol-3-yl]pyrimidin-4-amine

4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (70.0 mg, 335 μmol)and 4-ethyl-5-(4-fluoro-2-methylphenyl)-1H-pyrazol-3-amine (147 mg, 671μmol) are charged in a flask with NMP (700 μl). At room tempertaure,aqueous hydrochloric acid (84 μl, 12 M, 1.0 mmol) is added, and thereaction mixture is heated in a microwave for 1 h to 200° C. Thereaction mixture was directly purified by preparative HPLC (ChromatorexC18 10μ 125×40 mm gradient A=water +0.5% formic acid, B=acetonitrle, 0min=5% B, 3 min 25% B wash, then injection, 3 min 25% B, 20 min=75% B,20.1 min=95% B, 25 min=95% B, 25.1 min=end, flow 75 mL/min, detection at210 nm) to obtain 29.0 mg (100% purity, 22% yield) as desired product.

LC-MS (method 11): R_(t)=1.42 min; MS (ESIneg): m/z=390 [M−H]⁻

¹H-NMR (400 MHz, DMSO-d₆) δ [ppm]: −0.008 (2.23), 0.007 (2.04), 0.845(3.98), 0.864 (8.90), 0.882 (4.12), 2.172 (16.00), 2.212 (15.63), 2.254(0.97), 2.273 (2.74), 2.292 (2.69), 2.311 (0.89), 2.329 (0.40), 2.627(15.30), 5.754 (0.76), 6.125 (4.08), 7.113 (0.54), 7.133 (1.12), 7.155(0.66), 7.222 (0.99), 7.245 (1.03), 7.295 (1.10), 7.311 (1.31), 7.332(0.92), 7.459 (0.61), 8.461 (3.10), 9.360 (1.06), 12.511 (0.57).

Example 132N-[4-chloro-1-(2,2-difluoroethyl)-5-(4-fluorophenyl)-1H-pyrazol-3-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

The described product was prepared in a manner analogous to thatdescribed in the preparation ofN-[4-cyclopropyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3-methyl-1H-indazol-1-yl)pyrimidin-4-aminestarting from4-chloro-1-(2,2-difluoroethyl)-5-(4-fluorophenyl)-1H-pyrazol-3-amine(95.0 mg, 345 μmol) and4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (79.1 mg, 379 μmol)to yield 74.3 mg (100% purity, 48% yield) of the desired product afterpurification by preparative HPLC (method: column: Reprosil C18; 10 μm;125×30 mm/flow: 45 ml/min/eluent: A=water (0.1% formic acid),B=acetonitril/gradient: 0.00-4.25 min=20% B, 4.50 min=70% B, 15.50min=85% B, 16.00-23.00 min=100% B, 23.00-27.00 min=20% B andsubsequently method 4)

LC-MS (method 11): R_(t)=1.51 min; MS (ESIpos): m/z=448 [M+H]⁺

¹H-NMR (600 MHz, DMSO-d₆) δ [ppm]: 2.19 (s, 3H), 2.63 (s, 3H), 4.49 (td,2H), 6.14 (s, 1H), 6.23-6.53 (m, 1H), 7.38 (s, 1H), 7.44 (t, 2H), 7.59(dd, 2H), 8.49 (s, 1H), 9.71 (s, 1H).

Example 1331-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3-methyl-1,5,6,7-tetrahydro-4H-indazol-4-one

1-(6-chloropyrimidin-4-yl)-3-methyl-1,5,6,7-tetrahydro-4H-indazol-4-one(300 mg, 1.14 mmol) was dissolved in 1,4-dioxane (3.0 mL) in around-bottom flask under an argon atmosphere and sodium phenolate (181mg, 1.56 mmol) was added. The reaction mixture was degassed with Ar for3 min. Tris(dibenzylideneacetone)dipalladium (14.3 mg, 15.6 μmol),XantPhos (18.0 mg, 31.1 μmol) and4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (228 mg, 1.04mmol) were added. The reaction mixture was heated to 90° C. and stirredvigorously overnight. After cooling to ambient temperature, the reactionmixture was filtered and concentrated. The residue was purified bypreparative HPLC (column: Chromatorex C18; 250*30 mm, 10 μM, flow 100mL/min, gradient acetonitrile/water (containing 0.1% trifluoroaceticacid) 10/90 to 95/5) to yield the desired product (148 mg, 32% yield).

LC-MS (method 10): R_(t)=2.06 min; MS (ESIpos): m/z=446 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.89 (t, 3H) 2.04-2.12(m, 2H) 2.27-2.35 (m, 2H) 2.38-2.46 (m, 5H) 3.39-3.47 (m, 2H) 3.66 (s,3H) 7.34-7.42 (m, 2H), 7.43 (s, 1H), 7.46-7.58 (m, 2H) 8.47-8.56 (m, 1H)9.48-9.59 (m, 1H)

Example 134(±)-1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,4-dimethyl-4,5,6,7-tetrahydro-1H-indazol-4-ol(racemate)

1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3-methyl-1,5,6,7-tetrahydro-4H-indazol-4-one(34.5 mg, 77.4 μmol) was dissolved in tetrahydrofuran (0.73 mL), cooledto 0° C. and MeMgBr in tetrahydrofuran (1.0 m, 310 μL, 310 μmol) wasadded dropwise. The reaction mixture was allowed to stir at ambienttemperature for 20 minutes. It was then recooled to 0° C., and further150 μL MeMgBr (1.0 m, 150 μL, 150 μmol) were added. The icebath wasremoved and the reaction mixture allowed to stir at ambient temperaturefor 20 minutes. It was then quenched by addition of saturated aqueousammonium chloride solution and extracted with ethyl acetate (3×). Thecombined organic phase layers were dried over sodium sulfate,concentrated and the residue purified by flash column chromatography(KP-Sil 10 g, cyclohexane/ethyl acetate gradient (12-100%, 10 CV) andethyl acetate (100%, 7 CV) to yield the desired product (19 mg, 53%yield).

LC-MS (method 9): R_(t)=1.03 min; MS (ESIpos): m/z=462 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (1.20), −0.008(10.10), 0.008 (8.65), 0.146 (1.12), 0.862 (3.46), 0.881 (7.96), 0.900(3.56), 1.157 (3.69), 1.175 (7.58), 1.193 (3.82), 1.398 (2.77), 1.408(11.45), 1.701 (3.76), 1.919 (0.61), 1.988 (13.89), 2.274 (0.86), 2.292(2.59), 2.313 (15.92), 2.328 (1.58), 2.366 (0.48), 2.524 (2.03), 2.670(0.76), 2.710 (0.48), 3.061 (2.34), 3.075 (1.25), 3.650 (16.00), 4.003(1.07), 4.021 (3.28), 4.039 (3.26), 4.056 (1.04), 4.686 (5.42), 5.754(1.04), 7.293 (2.70), 7.358 (1.98), 7.380 (4.50), 7.402 (2.72), 7.498(2.57), 7.512 (2.85), 7.520 (2.31), 7.534 (1.96), 8.398 (3.46), 9.279(2.70).

Example 1354-(3-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-4-methyl-1H-pyrazol-5-yl)benzonitrile

A microwave vial was charged with4-(3-amino-4-methyl-1H-pyrazol-5-yl)benzonitrile (100 mg, 504 μmol),4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (95.7 mg, 459 μmol)and sodium phenolate (79.9 mg, 688 μmol) and the contents were suspendedin 1,4-dioxane (1.1 mL). The reaction mixture was degassed with Ar for 3min. Tris(dibenzylideneacetone)dipalladium (5.46 mg, 5.96 μmol) andXantPhos (7.96 mg, 13.8 μmol) were added and the reaction mixturedegassed again for 1 min. The vial was sealed and heated at 85° C.overnight while vigorously shaking. After cooling to ambienttemperature, the reaction mixture was filtered, diluted withdimethylsulfoxide and purified by preparative HPLC (method 7) to yieldthe desired product (26 mg, 13% yield) along with its regioisomericcoupling product (6.3 mg, 3% yield)

LC-MS (method 11): R_(t)=1.27 min; MS (ESIneg): m/z=369 [M−H]⁻

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.66), 0.008(1.32), 2.115 (14.73), 2.173 (15.69), 2.228 (0.83), 2.243 (0.69), 2.524(0.77), 2.628 (16.00), 2.664 (0.73), 2.678 (0.94), 6.131 (2.87), 7.455(0.77), 7.803 (1.42), 7.822 (1.81), 7.899 (0.69), 7.972 (1.91), 7.991(1.52), 8.467 (1.59), 9.445 (1.27), 13.107 (1.30).

Example 136 ethyl1-(6-{[5-(4-cyanophenyl)-4-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

A microwave vial was charged with (100 mg, 504 μmol), ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (156mg, 555 μmol) and sodium phenolate (87.8 mg, 757 μmol) and the contentswere suspended in 1,4-dioxane (1.2 mL). The reaction mixture wasdegassed with argon for 3 min. Tris(dibenzylideneacetone)dipalladium(6.01 mg, 6.56 μmol) and XantPhos (8.76 mg, 15.1 μmol) were added andthe reaction mixture degassed again for 1 min. The vial was sealed andheated at 85° C. overnight while vigorously shaking. After cooling toambient temperature, the reaction mixture was filtered, diluted withdimethylsulfoxide and purified by preparative HPLC (method 7) to yieldthe desired product (30.3 mg, 13% yield) along with the regioisomericcoupling product (6.2 mg, 3% yield).

LC-MS (Method 10): R_(t)=1.96 min; MS (ESIpos): m/z=443 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.47), −0.008(4.24), 0.008 (3.91), 0.146 (0.47), 1.288 (6.31), 1.306 (13.40), 1.324(6.60), 1.647 (1.03), 2.119 (13.50), 2.372 (16.00), 2.898 (15.22), 4.228(1.81), 4.245 (5.69), 4.263 (5.66), 4.281 (1.80), 7.368 (0.79), 7.385(0.81), 7.398 (0.99), 7.488 (0.58), 7.821 (1.73), 7.856 (0.68), 7.872(0.47), 7.969 (1.96), 8.550 (2.08), 9.666 (0.94), 13.129 (0.98).

Example 1374-(3-{[6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-4-methyl-1H-pyrazol-5-yl)benzonitrile

A microwave vial was charged with4-(3-amino-4-methyl-1H-pyrazol-5-yl)benzonitrile (100 mg, 504 μmol),4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (135 mg,555 μmol) and sodium phenolate (87.8 mg, 757 μmol) and the contents weresuspended in 1,4-dioxane (1.2 mL). The reaction mixture was degassedwith Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (6.01 mg, 6.56μmol) and XantPhos (8.76 mg, 15.1 μmol) were added and the reactionmixture was degassed again for 1 min. The vial was sealed and heated at85° C. overnight while vigorously shaking. After cooling to ambienttemperature, the reaction mixture was filtered, diluted withdimethylsulfoxide and purified by preparative HPLC (method 7) to yieldthe desired product (26.8 mg, 13% yield) along with its regioisomericcoupling product (5.8 mg, 3% yield).

LC-MS (method 10): R_(t)=2.10 min; MS (ESIpos): m/z=405 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.150 (0.73), −0.008(6.39), 0.008 (5.90), 0.146 (0.70), 2.115 (13.04), 2.211 (13.77), 2.328(0.51), 2.366 (0.48), 2.646 (16.00), 2.710 (0.46), 7.341 (0.53), 7.381(0.64), 7.465 (1.13), 7.478 (1.16), 7.780 (0.67), 7.798 (2.87), 7.819(3.60), 7.905 (1.13), 7.973 (3.35), 7.993 (2.66), 8.501 (2.25), 9.572(2.12), 13.122 (1.99).

Example 1381-[1-(6-{[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]cyclopropanol

In a flame-dried schlenk tube, ethyl1-(6-{[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(30.0 mg, 66.7 μmol) was dissolved in tetrahydrofuran (630 μL, 7.7 mmol)and the resulting solution cooled to 0° C. Titanium tetraisopropoxide(22 μl, 73 μmol) was added slowly via syringe. After 5 min, a solutionof ethylmagnesium bromide (1.0 M in tetrahydrofuran, 230 μl, 230 μmol)was added dropwise and the reaction mixture stirred for 3 h at 0° C. Theice-bath was then removed and the reaction mixture allowed to stirovernight at ambient temperature. It was quenched by addition ofsaturated aqueous ammonium chloride solution and extracted with ethylacetate (3×). The combined organic phase extracts washed with brine,dried over sodium sulfate and concentrated. The residue was purified bypreparative HPLC (column: Chromatorex C18; 125*40 mm, 10 μM, flow 100mL/min, gradient acetonitrile/water (containing 0.1% trifluoroaceticacid) 10/90 to 95/5) to yield the desired product (4.4 mg, 15% yield)after lyophilisation.

LC-MS (method 10): R_(t)=1,77 min; MS (ESIpos): m/z=434 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.006 (2.48), 0.645(1.48), 0.654 (4.27), 0.658 (3.94), 0.667 (1.54), 0.932 (1.65), 0.940(4.25), 0.944 (3.82), 0.954 (1.33), 1.848 (14.25), 2.276 (15.49), 2.362(0.78), 2.635 (0.51), 2.702 (16.00), 3.928 (1.77), 7.361 (3.65), 7.379(5.00), 7.397 (2.75), 7.512 (2.82), 7.523 (3.14), 7.529 (2.55), 7.540(2.09), 8.452 (4.04), 9.396 (2.97).

Example 1396-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]-N-[3-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-5-yl]pyrimidin-4-amine

A microwave vial was charged with3-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-5-amine (80.0 mg, 390 μmol),4-chloro-6-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine(120 mg, 429 μmol) and sodium phenolate (67.9 mg, 585 μmol) and thecontents were suspended in 1,4-dioxane (1.0 mL). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium(4.64 mg, 5.07 μmol) and XantPhos (6.77 mg, 11.7 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously shaking. After coolingto ambient temperature, the reaction mixture was filtered, diluted withdimethylsulfoxide and purified by preparative HPLC (method 4) to yieldthe desired product (57 mg, 32% yield) as a white powder.

LC-MS (method 10): R_(t)=2.31 min; MS (ESIpos): m/z=448 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.017 (16.00), 2.073(1.20), 2.280 (2.24), 2.328 (0.43), 2.680 (1.03), 3.664 (7.81), 7.247(1.79), 7.269 (3.60), 7.291 (2.03), 7.698 (1.37), 7.713 (1.96), 7.730(1.32), 7.901 (1.10), 8.032 (2.19), 8.163 (1.02), 8.528 (0.43), 9.677(0.67).

Example 1406-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]-N-[5-(4-fluorophenyl)-4-methyl-1H-pyrazol-3-yl]pyrimidin-4-amine

A microwave vial was charged with5-(4-fluorophenyl)-4-methyl-1H-pyrazol-3-amine (100 mg, 523 μmol),4-chloro-6-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine(161 mg, 575 μmol) and sodium phenolate (91.1 mg, 784 μmol) and thecontents were suspended in 1,4-dioxane (1.0 mL). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium(6.23 mg, 6.80 μmol) and XantPhos (9.08 mg, 15.7 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously shaking. After coolingto ambient temperature, the reaction mixture was filtered, diluted withdimethylsulfoxide and purified by preparative HPLC (method 5) to yieldthe desired product (11.8 mg, 4% yield) as a white powder along with theregioisomeric coupling product (26.0 mg, 11% yield).

LC-MS (method 10): R_(t)=2.21 min; MS (ESIpos): m/z=434 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.08 (s, 3H), 2.27 (s,3H), 7.32-7.39 (m, 2H), 7.44-7.61 (m, 1H), 7.60-7.66 (m, 2H), 8.04 (t,J=51.4 Hz, 1H), 8.52 (s, 1H), 9.72 (br s, 1H), 12.88 (br s, 1H).

Example 1414-[1-(cyclopropylmethyl)-5-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-4-methyl-1H-pyrazol-3-yl]benzonitrile

A solution of 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (1.50g, 7.21 mmol) in 1,4-dioxane (34 ml) was degassed with argon and heatedto an internal temperature of 85° C. To the heated solution was added4-[5-amino-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(2.00 g, 7.93 mmol), tris(dibenzylidenaceton)dipalladium (198 mg, 216μmol), Xantphos (229 mg, 432 μmol) and finally sodium phenolate (920 mg,7.93 mmol) before heating at 85° C. for an additional 30 minutes. Thereaction mixture was added to a saturated solution of sodium hydrogencarbonate (11 mL), and the solution extracted three times with ethylacetate. The combined organic phase s were washed with a saturatedsolution of sodium carbonate, dried with sodium sulfate and concentratedin vacuo. The crude product was purified by flash-chromatography onsilica gel (gradient 10% to 80% ethylacetate in cyclohexane, column:Biotage SNAP Ultra 100 g) and the residue washed with pentane to yield2.04 g (100% purity, 67% yield) of the desired product.

LC-MS (Method 9): R_(t)=1.14 min; MS (ESIpos): m/z=425 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.306 (2.74), 0.318(3.02), 0.433 (2.68), 0.453 (2.86), 1.177 (0.42), 1.191 (0.78), 1.198(0.71), 1.209 (1.08), 1.222 (0.68), 1.229 (0.72), 2.063 (16.00), 2.171(3.52), 2.629 (15.52), 3.861 (2.69), 3.878 (2.64), 5.754 (0.46), 6.145(3.06), 7.886 (1.12), 7.907 (11.00), 7.934 (1.02), 8.461 (0.80), 9.420(0.95).

Example 1424-[1-(cyclopropylmethyl)-5-({6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-yl}amino)-4-methyl-1H-pyrazol-3-yl]benzonitrile

A microwave vial was charged with4-[5-amino-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(100 mg, 396 μmol),4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (107mg, 436 μmol) and sodium phenolate (69.0 mg, 594 μmol) and the contentswere suspended in 1,4-dioxane (1.0 mL). The reaction mixture wasdegassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (4.72mg, 5.15 μmol) and XantPhos (6.88 mg, 11.9 μmol) were added and thereaction mixture was degassed again for 1 min. The vial was sealed andheated at 85° C. overnight while vigorously shaking. After cooling toambient temperature, the reaction mixture was filtered, diluted withdimethylsulfoxide and purified by preparative HPLC (method 4) to yieldthe desired product (31 mg, 15% yield).

LC-MS (method 9): R_(t)=1.18 min; MS (ESIpos): m/z=461 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.26-0.35 (m, 2H),0.40-0.49 (m, 2H), 1.14-1.27 (m, 1H), 2.03-2.10 (m, 3H), 2.19-2.38 (m,3H), 3.80-3.94 (m, 2H), 6.79 (s, 1H), 7.64-7.99 (m, 5H), 8.27-8.71 (m,1H), 9.37-9.90 (m, 1H).

Example 143N-[1-(cyclopropylmethyl)-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (79.0 mg, 379 μmol),1-(cyclopropylmethyl)-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-amine (120mg, 90% purity, 416 μmol) and sodium phenolate (65.9 mg, 568 μmol) andthe contents were suspended in 1,4-dioxane (2.7 ml, 32 mmol). Thereaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (4.51 mg, 4.92 μmol) and Xantphos(6.57 mg, 11.4 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with saturated sodium bicarbonate solutionand extracted with ethyl acetate (2×). The combined organic phases weredried over sodium sulfate and concentrated under reduced pressure. Thecrude product was purified by preparative HPLC (method 4) to yield thedesired product (84.0 mg, 51%).

LC-MS (method 10): R_(t)=2.44 min; MS (ESIpos): m/z=432 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.90), 0.008(0.76), 0.184 (0.66), 0.196 (2.68), 0.210 (2.82), 0.222 (0.79), 0.420(0.93), 0.431 (2.52), 0.435 (2.59), 0.440 (1.38), 0.451 (2.68), 0.454(2.54), 0.466 (0.78), 0.869 (3.83), 0.888 (8.83), 0.907 (3.96), 1.033(0.63), 1.040 (0.63), 1.052 (0.99), 1.064 (0.59), 1.070 (0.60), 2.168(16.00), 2.285 (0.93), 2.303 (2.74), 2.322 (2.75), 2.341 (0.87), 2.524(0.40), 2.628 (14.84), 3.759 (4.68), 3.776 (4.61), 6.125 (3.96), 7.354(2.04), 7.377 (4.90), 7.399 (3.06), 7.469 (2.92), 7.475 (1.31), 7.483(3.30), 7.491 (2.54), 7.500 (0.99), 7.505 (2.08), 7.595 (0.68), 8.456(3.32), 9.399 (3.28).

Example 1446-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-[1-(cyclopropylmethyl)-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (92.0 mg,379 μmol),1-(cyclopropylmethyl)-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-amine (120mg, 90% purity, 416 μmol) and sodium phenolate (65.9 mg, 568 μmol) andthe contents were suspended in 1,4-dioxane (2.7 ml, 32 mmol). Thereaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (4.51 mg, 4.92 μmol) and Xantphos(6.57 mg, 11.4 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with saturated sodium bicarbonate solutionand extracted with ethyl acetate (2×). The combined organic phases weredried over sodium sulfate and concentrated under reduced pressure. Thecrude product was purified by preparative HPLC (method 5) to yield thedesired product (72.0 mg, 41%).

LC-MS (method 10): R_(t)=2.72 min; MS (ESIpos): m/z=466 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.02), 0.008(0.94), 0.204 (2.11), 0.215 (2.23), 0.423 (0.76), 0.433 (2.11), 0.437(2.18), 0.453 (2.25), 0.468 (0.65), 0.868 (3.19), 0.887 (7.26), 0.905(3.27), 1.030 (0.57), 1.037 (0.56), 1.049 (0.85), 1.061 (0.52), 1.067(0.52), 2.206 (14.04), 2.289 (0.76), 2.307 (2.14), 2.326 (2.20), 2.345(0.69), 2.649 (16.00), 3.758 (3.91), 3.776 (3.85), 7.355 (1.78), 7.377(4.33), 7.399 (2.75), 7.469 (2.53), 7.475 (1.19), 7.483 (2.87), 7.491(2.22), 7.505 (1.78), 8.493 (3.22), 9.531 (2.05).

Example 145 ethyl1-(6-{[1-(cyclopropylmethyl)-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

A microwave vial was charged ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (106mg, 379 μmol),1-(cyclopropylmethyl)-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-amine (120mg, 90% purity, 416 μmol) and sodium phenolate (65.9 mg, 568 μmol) andthe contents were suspended in 1,4-dioxane (2.7 ml, 32 mmol). Thereaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (4.51 mg, 4.92 μmol) and Xantphos(6.57 mg, 11.4 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with saturated sodium bicarbonate solutionand extracted with ethyl acetate (2×). The combined organic phases weredried over sodium sulfate and concentrated under reduced pressure. Thecrude product was purified by preparative HPLC (method 5) to yield thedesired product (82.0 mg, 43%).

LC-MS (method 10): R_(t)=2.58 min; MS (ESIpos): m/z=504 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.008 (0.50), 0.192(2.20), 0.204 (2.31), 0.412 (0.79), 0.423 (2.28), 0.426 (2.27), 0.443(2.39), 0.458 (0.65), 0.873 (3.22), 0.892 (7.18), 0.910 (3.31), 1.028(0.60), 1.035 (0.59), 1.047 (0.92), 1.058 (0.54), 1.065 (0.57), 1.289(4.41), 1.307 (9.29), 1.324 (4.50), 2.296 (0.76), 2.314 (2.05), 2.333(2.10), 2.367 (13.94), 2.905 (16.00), 3.756 (3.98), 3.773 (3.91), 4.228(1.32), 4.246 (4.14), 4.264 (4.09), 4.281 (1.28), 7.355 (1.79), 7.377(4.26), 7.399 (2.67), 7.469 (2.57), 7.483 (2.94), 7.491 (2.20), 7.505(1.77), 8.539 (3.05), 9.625 (1.56).

Example 146(rac)-1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,4-dimethyl-1,4,5,6-tetrahydrocyclopenta[c]pyrazol-4-ol

1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3-methyl-5,6-dihydrocyclopenta[c]pyrazol-4(1H)-one(46.0 mg, 107 μmol) was dissolved in tetrahydrofuran and cooled with awaterbath of 20° C. A solution of methylmagnesium bromide (1.0 M intetrahydrofuran, 430 μl, 430 μmol) was added dropwise. After 30 minutesstirring at 20° C., a second aliquot of methylmagnesium bromide (1.0 Min tetrahydrofuran, 250 μl, 250 μmol) was added. The reaction mixturewas stirred for 20 minutes at ambient temperature before being quenchedby addition of saturated aqueous ammonium chloride solution. It wasextracted with ethyl acetate (3×), the combined organic phase extractswere washed with brine, dried over sodium sulfate and concentrated. Theresidue was purified by flash column chromatography (KP Sil 10 g,cyclohexane/ethyl acetate gradient 70/30 to 0/100 10CV, 0/100 5 CV,flow: 36 mL/min). The product-containing fractions were combined,concentrated and dried under vacuum to yield the desired product (34 mg,66% yield).

LC-MS (method 11): R_(t)=1.29 min; MS (ESIneg): m/z=446 [M−H]⁻

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.21 (s, 3H), 2.24-2.38(m, 2H), 2.40-2.48 (m, 1H), 2.90-3.22 (m, 2H), 3.66 (s, 3H), 4.95 (s,1H), 7.22 (s, 1H), 7.31-7.60 (m, 4H), 8.39 (s, 1H), 9.31 (s, 1H).

Example 147 ethyl1-(6-{[1-(cyclopropylmethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

A microwave vial was charged ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (88.6mg, 315 μmol),1-(cyclopropylmethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-amine (120mg, 75% purity, 347 μmol) and sodium phenolate (54.9 mg, 473 μmol) andthe contents were suspended in 1,4-dioxane (2.2 ml, 26 mmol). Thereaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (3.76 mg, 4.10 μmol) and Xantphos(5.48 mg, 9.46 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with saturated sodium bicarbonate solutionand extracted with ethyl acetate (2×). The combined organic phases weredried over sodium sulfate and concentrated under reduced pressure. Thecrude product was purified by preparative HPLC (method 4) to yield thedesired product (75.0 mg, 47%).

LC-MS (method 10): R_(t)=2.55 min; MS (ESIpos): m/z=504 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.297 (3.93), 0.307(3.97), 0.436 (4.33), 0.456 (4.33), 0.974 (5.80), 0.993 (11.75), 1.012(5.63), 1.091 (0.53), 1.174 (0.73), 1.187 (1.25), 1.194 (1.23), 1.205(1.69), 1.217 (1.14), 1.223 (1.14), 1.235 (0.67), 1.287 (4.85), 1.304(8.86), 1.322 (4.54), 2.369 (2.80), 2.461 (3.89), 2.479 (4.21), 2.912(16.00), 3.798 (3.41), 3.813 (3.27), 4.227 (1.72), 4.245 (4.29), 4.262(4.15), 4.280 (1.49), 7.254 (3.49), 7.276 (6.81), 7.298 (3.80), 7.671(2.52), 7.686 (3.35), 7.703 (2.22), 8.523 (0.59), 9.483 (0.54).

Example 1486-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]-N-[1-(cyclopropylmethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]pyrimidin-4-amine

A microwave vial was charged4-chloro-6-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine(88.0 mg, 315 μmol),1-(cyclopropylmethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-amine (120mg, 75% purity, 347 μmol) and sodium phenolate (54.9 mg, 473 μmol) andthe contents were suspended in 1,4-dioxane (2.2 ml, 26 mmol). Thereaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (3.76 mg, 4.10 μmol) and Xantphos(5.48 mg, 9.46 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with saturated sodium bicarbonate solutionand extracted with ethyl acetate (2×). The combined organic phases weredried over sodium sulfate and concentrated under reduced pressure. Thecrude product was purified by preparative HPLC (method 5) to yield thedesired product (62.0 mg, 39%).

LC-MS (method 10): R_(t)=2.60 min; MS (ESIpos): m/z=502 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.300 (4.54), 0.434(5.29), 0.453 (5.45), 0.969 (7.46), 0.988 (16.00), 1.007 (7.69), 1.091(0.40), 1.195 (2.11), 2.288 (2.75), 2.367 (0.84), 2.456 (3.77), 2.476(4.00), 2.670 (0.66), 2.711 (0.54), 3.806 (3.68), 7.256 (4.08), 7.278(8.28), 7.300 (4.79), 7.688 (3.57), 7.904 (2.41), 8.036 (4.82), 8.167(2.16), 8.494 (0.70), 9.547 (0.63).

Example 149 ethyl1-(6-{[3-(4-cyanophenyl)-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

A round-bottom flask was charged with4-[5-amino-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(1.00 g, 3.96 mmol), ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (1.22g, 4.36 mmol) and sodium phenolate (506 mg, 4.36 mmol) and the contentswere suspended in 1,4-dioxane (1.0 mL). The reaction mixture wasdegassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (47.2mg, 51.5 μmol) and XantPhos (68.8 mg, 119 μmol) were added and thereaction mixture was degassed again for 1 min. The reaction mixture washeated at 85° C. overnight while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with water andextracted with ethyl acetate. The organic phase extract was dried oversodium sulfate and concentrated. The residue was purified by flashcolumn chromatography (SNAP Ultra 50 g, gradient cyclohexane/ethylacetate 88/12 to 0/100) to yield the desired product (917 mg, 47%yield).

LC-MS (method 11): R_(t)=1.54 min; MS (ESIpos): m/z=497 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.42), −0.008(3.61), 0.008 (3.11), 0.146 (0.42), 0.307 (2.56), 0.320 (2.84), 0.436(2.57), 0.456 (2.76), 1.157 (0.91), 1.175 (1.98), 1.193 (1.58), 1.199(0.74), 1.211 (1.11), 1.231 (0.71), 1.288 (3.61), 1.306 (7.36), 1.323(3.69), 1.398 (2.60), 1.988 (3.20), 2.064 (16.00), 2.328 (0.77), 2.376(2.12), 2.670 (0.52), 2.911 (12.61), 3.568 (2.16), 3.865 (2.23), 3.882(2.21), 4.021 (0.75), 4.039 (0.77), 4.229 (1.08), 4.247 (3.23), 4.265(3.23), 4.282 (1.07), 7.885 (0.77), 7.907 (13.79), 7.931 (0.82), 8.534(0.44), 9.582 (0.41).

Example 1504-[5-{[6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile

A microwave vial was charged with4-[5-amino-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(100 mg, 396 μmol),4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (106 mg,436 μmol) and sodium phenolate (69.0 mg, 594 μmol) and the contents weresuspended in 1,4-dioxane (1.1 mL). The reaction mixture was degassedwith Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (4.72 mg, 5.15μmol) and XantPhos (6.88 mg, 11.9 μmol) were added and the reactionmixture was degassed again for 1 min. The vial was sealed and heated at85° C. overnight while vigorously shaking. After cooling to ambienttemperature, the reaction mixture was filtered, diluted withdimethylsulfoxide and purified by preparative HPLC (method 4) to yieldan impure product fraction (102 mg). Upon attempted dissolution indimethylsulfoxide, a white solid remains and was filtered off. Thefiltrate was further purified by preparative HPLC (method 8) to yieldthe desired product (51 mg, 27% yield).

LC-MS (method 10): R_(t)=2.54 min; MS (ESIpos): m/z=459 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (2.32), 0.008(2.05), 0.303 (2.08), 0.315 (2.29), 0.431 (2.13), 0.451 (2.29), 1.187(0.59), 1.194 (0.56), 1.206 (0.89), 1.218 (0.53), 1.224 (0.55), 2.061(14.73), 2.211 (2.16), 2.523 (0.98), 2.648 (16.00), 2.670 (0.55), 3.860(1.98), 3.878 (1.93), 7.887 (0.74), 7.907 (10.23), 7.932 (0.67), 8.495(0.46), 9.518 (0.44).

Example 151 ethyl1-(6-{[1-(cyclopropylmethyl)-5-(4-fluorophenyl)-4-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

A microwave vial was charged ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (143mg, 511 μmol),1-(cyclopropylmethyl)-5-(4-fluorophenyl)-4-methyl-1H-pyrazol-3-amine(138 mg, 562 μmol) and sodium phenolate (88.9 mg, 766 μmol) and thecontents were suspended in 1,4-dioxane (2.3 ml, 27 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (6.08 mg, 6.64 μmol) and Xantphos(8.86 mg, 15.3 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with saturated sodium bicarbonate solutionand extracted with ethyl acetate (2×). The combined organic phases weredried over sodium sulfate and concentrated under reduced pressure. Thecrude product was purified by preparative HPLC (method: column: ReprosilC18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent: A=water (0.1% formicacid), B=acetonitrile/gradient: 0.00-4.25 min=20% B, 4.50 min=30% B,19.00-22.50 min=100% B, 22.75-25.00 min=20%) to yield the desiredproduct (34.7 mg, 14%).

LC-MS (method 10): R_(t)=2.61 min; MS (ESIpos): m/z=490 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (3.04), 0.008(1.96), 0.201 (1.87), 0.213 (1.91), 0.407 (0.87), 0.418 (2.07), 0.422(2.16), 0.438 (2.12), 0.453 (0.59), 1.029 (0.54), 1.049 (0.82), 1.289(4.51), 1.307 (9.63), 1.325 (4.58), 1.504 (0.77), 1.860 (8.28), 2.002(0.48), 2.328 (0.55), 2.370 (13.74), 2.523 (1.50), 2.670 (0.54), 2.905(16.00), 3.802 (3.69), 3.819 (3.71), 4.229 (1.29), 4.246 (4.18), 4.264(4.11), 4.282 (1.29), 7.355 (1.79), 7.377 (4.20), 7.400 (2.64), 7.477(2.61), 7.483 (1.24), 7.491 (2.83), 7.499 (2.26), 7.513 (1.84), 8.544(2.66), 9.669 (1.89).

Example 152 ethyl1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

A microwave vial was charged ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (112mg, 399 μmol),1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine(108 mg, 439 μmol) and sodium phenolate (69.4 mg, 598 μmol) and thecontents were suspended in 1,4-dioxane (1.8 ml, 21 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (4.75 mg, 5.18 μmol) and Xantphos(6.92 mg, 12.0 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with saturated sodium bicarbonate solutionand extracted with ethyl acetate (2×). The combined organic phases weredried over sodium sulfate and concentrated under reduced pressure. Thecrude product was purified by preparative HPLC (method: column: ReprosilC18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent: A=water (0.1% formicacid), B=acetonitrile/gradient: 0.00-4.25 min=20% B, 4.50 min=30% B,19.00-22.50 min=100% B, 22.75-25.00 min=20%) to yield the desiredproduct (133 mg, 68%).

LC-MS (method 11): R_(t)=1.59 min; MS (ESIpos): m/z=490 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.294 (2.81), 0.306(3.08), 0.426 (2.83), 0.446 (3.02), 1.073 (0.47), 1.091 (0.94), 1.109(0.47), 1.167 (0.43), 1.180 (0.79), 1.186 (0.75), 1.198 (1.16), 1.216(0.75), 1.230 (0.43), 1.287 (3.77), 1.304 (7.56), 1.322 (3.86), 2.009(16.00), 2.368 (2.59), 2.388 (2.94), 2.910 (13.62), 2.933 (1.71), 3.375(0.51), 3.392 (0.49), 3.830 (2.49), 3.847 (2.46), 4.228 (1.20), 4.245(3.43), 4.263 (3.47), 4.280 (1.24), 7.252 (2.49), 7.274 (5.14), 7.296(2.81), 7.312 (0.56), 7.711 (1.73), 7.726 (2.31), 7.746 (1.59), 8.533(0.51), 10.193 (0.66).

Example 153 ethyl1-(6-{[4-chloro-1-(cyclopropylmethyl)-5-(4-fluorophenyl)-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

A microwave vial was charged ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (121mg, 429 μmol),4-chloro-1-(cyclopropylmethyl)-5-(4-fluorophenyl)-1H-pyrazol-3-amine(126 mg, 472 μmol) and sodium phenolate (74.8 mg, 644 μmol) and thecontents were suspended in 1,4-dioxane (1.9 ml, 22 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (5.11 mg, 5.58 μmol) and Xantphos(7.45 mg, 12.9 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with saturated sodium bicarbonate solutionand extracted with ethyl acetate (2×). The combined organic phases weredried over sodium sulfate and concentrated under reduced pressure. Thecrude product was purified by preparative HPLC (method: column: ReprosilC18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent: A=water (0.1% formicacid), B=acetonitrile/gradient: 0.00-4.25 min=20% B, 4.50 min=30% B,19.00-22.50 min=100% B, 22.75-25.00 min=20%) to yield the desiredproduct (105 mg, 44%).

LC-MS (method 11): R_(t)=1.71 min; MS (ESIpos): m/z=510 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.197 (1.02), 0.209(3.23), 0.221 (3.24), 0.233 (0.90), 0.436 (1.20), 0.447 (2.91), 0.450(2.97), 0.467 (2.96), 0.482 (0.86), 1.054 (0.48), 1.066 (0.80), 1.073(0.83), 1.085 (1.11), 1.092 (0.77), 1.103 (0.70), 1.290 (4.80), 1.308(9.29), 1.326 (4.52), 2.377 (14.64), 2.911 (16.00), 3.893 (4.78), 3.911(4.59), 4.230 (1.56), 4.248 (4.26), 4.266 (4.09), 4.284 (1.30), 7.407(2.23), 7.429 (4.61), 7.451 (2.68), 7.518 (1.20), 7.586 (2.88), 7.600(3.19), 7.608 (2.69), 7.622 (2.14), 8.573 (3.31), 9.806 (3.24).

Example 1544-[5-({6-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-yl}amino)-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile

A microwave vial was charged with4-[5-amino-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(200 mg, 793 μmol),4-chloro-6-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine(243 mg, 872 μmol) and sodium phenolate (101 mg, 872 μmol) and thecontents were suspended in 1,4-dioxane (2.2 mL). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium(9.44 mg, 10.3 μmol) and XantPhos (13.8 mg, 23.8 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously shaking. After coolingto ambient temperature, the reaction mixture was concentrated andpurified by flash column chromatography (KPSil 25 g, gradientcyclohexane/ethyl acetate 90/10 to 40:60) to yield the desired product(110 mg, 26% yield) that was dried overnight under high-vacuum.

LC-MS (method 10): R_(t)=2.40 min; MS (ESIpos): m/z=495 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.26-0.38 (m, 2H),0.41-0.50 (m, 2H), 1.12-1.30 (m, 1H), 2.06 (s, 3H), 2.18-2.38 (br s,3H), 3.79-3.95 (m, 2H), 7.91 (s, 4H), 7.87-8.20 (m, 1H), 8.34-8.84 (m,1H), 9.40-10.06 (m, 1H).

Example 155 ethyl1-(6-{[4-ethyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

A microwave vial was charged ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (200mg, 712 μmol), 4-ethyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-amine(172 mg, 784 μmol) and sodium phenolate (91.0 mg, 784 μmol) and thecontents were suspended in 1,4-dioxane (3.3 ml, 39 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (8.48 mg, 9.26 μmol) and Xantphos(12.4 mg, 21.4 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with saturated sodium bicarbonate solutionand extracted with ethyl acetate (2×). The combined organic phases weredried over sodium sulfate and concentrated under reduced pressure. Thecrude product was purified by preparative HPLC (method: column: ReprosilC18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent: A=water (0.1% formicacid), B=acetonitrile/gradient: 0.00-4.25 min=20% B, 4.50 min=30% B,19.00-22.50 min=100% B, 22.75-25.00 min=20%)) to yield the desiredproduct (194 mg, 54%).

LC-MS (method 10): R_(t)=2.30 min; MS (ESIpos): m/z=464 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.972 (4.73), 0.991(10.20), 1.009 (4.99), 1.289 (4.19), 1.307 (8.39), 1.324 (4.25), 2.378(3.04), 2.448 (1.27), 2.466 (3.16), 2.632 (0.44), 2.915 (16.00), 3.644(12.19), 3.675 (0.53), 4.230 (1.29), 4.247 (3.79), 4.265 (3.77), 4.283(1.31), 7.247 (2.63), 7.269 (5.31), 7.291 (2.96), 7.342 (1.37), 7.382(1.53), 7.465 (2.40), 7.478 (1.55), 7.489 (0.48), 7.649 (2.07), 7.663(2.75), 7.669 (2.67), 7.684 (1.97), 7.782 (1.44), 7.794 (1.37), 7.807(1.10), 7.813 (1.20), 7.821 (1.27), 8.544 (0.78), 9.540 (0.99).

Example 156 ethyl1-(6-{[3-(4-cyanophenyl)-1-(cyclopropylmethyl)-4-ethyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

A microwave vial was charged ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (125mg, 445 μmol),4-[5-amino-1-(cyclopropylmethyl)-4-ethyl-1H-pyrazol-3-yl]benzonitrile(130 mg, 490 μmol) and sodium phenolate (77.5 mg, 668 μmol) and thecontents were suspended in 1,4-dioxane (2.5 ml, 29 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (5.30 mg, 5.79 μmol) and Xantphos(7.73 mg, 13.4 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with water and extracted with ethyl acetate(2×). The combined organic phases were dried over Extrelute NT3 andconcentrated under reduced pressure. The crude product was purified bypreparative HPLC (method 5) to yield the desired product (117 mg, 49%).

LC-MS (method 10): R_(t)=2.37 min; MS (ESIpos): m/z=511 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.312 (3.56), 0.322(3.61), 0.447 (3.88), 0.467 (3.96), 0.982 (0.94), 0.994 (5.34), 1.013(11.32), 1.032 (5.43), 1.158 (0.48), 1.176 (0.96), 1.187 (0.70), 1.199(1.17), 1.206 (1.11), 1.218 (1.65), 1.233 (1.29), 1.249 (0.71), 1.289(4.70), 1.306 (9.22), 1.324 (4.73), 1.990 (1.33), 2.360 (2.77), 2.369(2.45), 2.405 (1.78), 2.915 (16.00), 2.953 (1.28), 3.833 (3.02), 3.848(2.93), 4.229 (1.41), 4.247 (4.01), 4.264 (4.04), 4.282 (1.50), 7.827(0.41), 7.865 (1.87), 7.887 (7.59), 7.898 (12.40), 7.919 (2.82), 7.941(0.83), 8.525 (0.65), 9.539 (0.55).

Example 1574-[5-{[6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-1-(cyclopropylmethyl)-4-ethyl-1H-pyrazol-3-yl]benzonitrile

A microwave vial was charged4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (125 mg,514 μmol),4-[5-amino-1-(cyclopropylmethyl)-4-ethyl-1H-pyrazol-3-yl]benzonitrile(151 mg, 566 μmol) and sodium phenolate (89.5 mg, 771 μmol) and thecontents were suspended in 1,4-dioxane (2.5 ml, 29 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (6.12 mg, 6.68 μmol) and Xantphos(8.93 mg, 15.4 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with water and extracted with ethyl acetate(2×).

The combined organic phases were dried over Extrelut NT3 andconcentrated under reduced pressure. The crude product was purified byflash chromatography on silica gel (dichloromethane/ethyl acetate) toyield the desired product (154 mg, 60%).

LC-MS (method 11): R_(t)=1.66 min; MS (ESIpos): m/z=473 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.310 (3.07), 0.319(3.06), 0.446 (3.43), 0.465 (3.34), 0.993 (4.36), 1.012 (8.85), 1.030(4.44), 1.092 (0.60), 1.185 (0.61), 1.197 (0.99), 1.205 (0.98), 1.216(1.31), 1.227 (0.95), 1.234 (0.95), 2.213 (2.52), 2.647 (16.00), 3.832(2.79), 3.847 (2.61), 5.756 (2.06), 7.869 (1.77), 7.890 (6.58), 7.899(9.32), 7.919 (1.99), 8.489 (0.65), 9.480 (0.56).

Example 158 ethyl1-(6-{[4-chloro-1-(cyclopropylmethyl)-3-(4-fluorophenyl)-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

A microwave vial was charged ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (81.4mg, 290 μmol),4-chloro-1-(cyclopropylmethyl)-3-(4-fluorophenyl)-1H-pyrazol-5-amine(84.8 mg, 319 μmol) and sodium phenolate (50.5 mg, 435 μmol) and thecontents were suspended in 1,4-dioxane (1.3 ml, 15 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (3.45 mg, 3.77 μmol) and Xantphos(5.04 mg, 8.70 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was purified by preparative HPLC (method: column:Reprosil C18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent: A=water (0.1%formic acid), B=acetonitrile/gradient: 0.00-4.25 min=20% B, 4.50 min=30%B, 19.00-22.50 min=100% B, 22.75-25.00 min=20%) to yield the desiredproduct (67.0 mg, 45%).

LC-MS (method 10): R_(t)=2.50 min; MS (ESIpos): m/z=510 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.318 (0.67), 0.330(2.81), 0.343 (3.10), 0.355 (0.96), 0.453 (0.84), 0.463 (2.49), 0.466(2.41), 0.483 (2.66), 0.498 (0.59), 1.158 (1.45), 1.176 (2.94), 1.194(1.59), 1.203 (0.40), 1.216 (0.69), 1.223 (0.68), 1.234 (1.09), 1.246(0.66), 1.254 (0.68), 1.292 (4.37), 1.309 (9.05), 1.327 (4.48), 1.989(5.37), 2.385 (6.60), 2.920 (16.00), 2.959 (0.50), 3.900 (3.00), 3.918(2.99), 4.004 (0.45), 4.021 (1.31), 4.039 (1.31), 4.057 (0.45), 4.234(1.31), 4.251 (3.99), 4.269 (3.96), 4.287 (1.26), 7.309 (2.28), 7.331(4.62), 7.353 (2.49), 7.896 (2.15), 7.910 (2.49), 7.918 (2.40), 7.932(2.04), 8.570 (1.50), 9.807 (1.22).

Example 1592-[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]propan-2-ol

Ethyl1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(5.00 g, 95% purity, 9.70 mmol) was dissolved in tetrahydrofuran (200mL) under an argon atmosphere and the resulting solution was cooled to0° C. A solution of bromo(methyl)magnesium (3.0 M, 16 ml, 49 mmol) wasadded dropwise and the reaction mixture was allowed to slowly reachambient temperature and was stirred overnight. The reaction was quenchedwith aqueous Na₂EDTA solution (10%, 50 mL) and stirring was continuedfor 30 min. After further dilution with water (200 mL), it was extractedwith ethyl acetate (200 mL). The organic phase extract was dried oversodium sulfate and concentrated. The residue was purified by flashcolumn chromatography (340 g silica gel, cyclohexane/ethyl acetate 1:1)to yield the desired product as a white solid (2.95 g, 64% yield).

LC-MS (method 11): R_(t)=1.38 min; MS (ESIneg): m/z=474 [M−H]⁻

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.67), 0.008(0.83), 0.280 (0.45), 0.293 (1.95), 0.305 (2.17), 0.316 (0.65), 0.424(1.88), 0.443 (2.02), 1.158 (2.16), 1.175 (4.48), 1.186 (0.60), 1.193(2.57), 1.209 (0.50), 1.217 (0.50), 1.465 (16.00), 1.989 (7.83), 2.005(11.66), 2.265 (2.42), 2.743 (11.95), 3.826 (1.94), 3.844 (1.91), 4.003(0.64), 4.021 (1.85), 4.039 (1.84), 4.057 (0.61), 4.855 (3.26), 7.249(1.70), 7.271 (3.50), 7.293 (1.90), 7.709 (1.39), 7.723 (1.71), 7.730(1.67), 7.744 (1.30), 8.461 (0.53), 9.361 (0.65).

Example 1602-[1-(6-{[4-chloro-1-(cyclopropylmethyl)-5-(4-fluorophenyl)-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]propan-2-ol

A sloution of ethyl1-(6-{[4-chloro-1-(cyclopropylmethyl)-5-(4-fluorophenyl)-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(93.0 mg, 182 μmol) in tetrahydrofuran (3.0 ml, 37 mmol) was treatedwith bromo(methyl)magnesium (210 3.0 M, 640 μmol) at 0° C. The mixturewas stirred at ambient temperature overnight. The mixture was dilutedwith water and purified by preparative HPLC (method: column: ReprosilC18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent: A=water (0.01% formicacid), B=acetonitrile/gradient: 0.00-5.00 min=10% B, 6.50 min=20% B,17.0-19.75 min=100% B, 19.75-23.00 min=90% B) to yield 44.4 mg (49%) ofthe desired product.

LC-MS (method 11): R_(t)=1.49 min; MS (ESIpos): m/z=496 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.202 (1.55), 0.215(1.68), 0.227 (0.48), 0.431 (0.44), 0.445 (1.36), 0.462 (1.40), 0.477(0.41), 1.080 (0.51), 1.091 (0.47), 1.472 (16.00), 2.274 (8.04), 2.742(8.49), 3.886 (2.30), 3.904 (2.27), 4.851 (3.25), 7.404 (1.12), 7.426(3.19), 7.448 (1.43), 7.580 (1.34), 7.594 (1.52), 7.602 (1.33), 7.615(1.07), 8.492 (2.10), 9.586 (2.06).

Example 1614-[1-(cyclopropylmethyl)-5-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-4-ethyl-1H-pyrazol-3-yl]benzonitrile

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (125 mg, 599 μmol),4-[5-amino-1-(cyclopropylmethyl)-4-ethyl-1H-pyrazol-3-yl]benzonitrile(176 mg, 659 μmol) and sodium phenolate (104 mg, 899 μmol) and thecontents were suspended in 1,4-dioxane (2.5 ml, 29 mmol).

The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (7.13 mg, 7.79 μmol) and Xantphos(10.4 mg, 18.0 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with saturated sodium bicarbonate solutionand extracted with ethyl acetate (2×). The combined organic phases weredried over sodium sulfate and concentrated under reduced pressure. Thecrude product was purified by preparative HPLC (method: column: ReprosilC18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent: A=water (0.01% formicacid), B=acetonitrile/gradient: 0.00-5.00 min=10% B, 6.50 min=20% B,17.0-19.75 min=100% B, 19.75-23.00 min=90% B) and additionally by flashchromatography on silica gel (dichloromethane/ethyl acetate) to yieldthe desired product (139 mg, 53%).

LC-MS (method 10): R_(t)=2.25 min; MS (ESIpos): m/z=439 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.01), 0.008(1.04), 0.309 (2.41), 0.321 (2.64), 0.443 (2.59), 0.463 (2.78), 0.994(3.93), 1.012 (8.83), 1.031 (4.12), 1.157 (0.73), 1.175 (1.53), 1.186(0.43), 1.193 (1.03), 1.205 (0.70), 1.216 (1.11), 1.228 (0.69), 1.235(0.73), 1.989 (2.71), 2.172 (2.35), 2.630 (16.00), 3.828 (2.17), 3.845(2.14), 4.021 (0.63), 4.039 (0.64), 6.144 (2.60), 7.868 (1.18), 7.889(5.74), 7.898 (9.64), 7.919 (1.68), 8.456 (0.67), 9.384 (0.69).

Example 162N-[1-(2,2-difluoroethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (70.4 mg, 338 μmol),1-(2,2-difluoroethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-amine (100mg, 371 μmol) and potassium phosphate (107 mg, 506 μmol) and thecontents were suspended in 1,4-dioxane (3.8 ml, 45 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (4.02 mg, 4.39 μmol) and Xantphos(5.86 mg, 10.1 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was purified by preparative HPLC (method: column:Reprosil C18; 10 μm; 125×40 mm/flow: 75 mL/min/solvent: A=water (0.1%formic acid), B=acetonitril/gradient: 0.00-5.50 min=10% B, 17.65-19.48min=95% B, 19.66 min=10% B) to yield the desired product (37.0 mg, 22%).

LC-MS (method 10): R_(t)=2.23 min; MS (ESIpos): m/z=442 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.70), 0.961(4.01), 0.979 (9.11), 0.998 (4.23), 1.356 (0.73), 2.181 (5.22), 2.450(0.95), 2.468 (2.96), 2.634 (16.00), 4.396 (0.76), 4.431 (1.33), 4.465(0.74), 6.151 (3.53), 6.206 (0.41), 6.216 (0.79), 6.344 (0.73), 6.353(1.56), 6.363 (0.75), 6.491 (0.73), 7.272 (2.55), 7.294 (5.18), 7.316(2.81), 7.342 (0.83), 7.382 (0.83), 7.461 (1.13), 7.465 (1.20), 7.478(0.73), 7.674 (2.03), 7.688 (2.48), 7.695 (2.32), 7.709 (1.82), 7.781(0.71), 7.790 (0.56), 7.794 (0.64), 7.807 (0.48), 7.814 (0.55), 7.821(0.59), 8.465 (1.62), 9.394 (2.57).

Example 1636-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-[1-(2,2-difluoroethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (82.1 mg,338 μmol),1-(2,2-difluoroethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-amine (100mg, 371 μmol) and potassium phosphate (107 mg, 506 μmol) and thecontents were suspended in 1,4-dioxane (2.4 ml, 28 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (4.02 mg, 4.39 μmol) and Xantphos(5.86 mg, 10.1 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was purified by preparative HPLC (method: column:Reprosil C18; 10 μm; 125×40 mm/flow: 75 mL/min/solvent: A=water (0.1%formic acid), B=acetonitril/gradient: 0.00-5.50 min=10% B, 17.65-19.48min=95% B, 19.66 min=10% B) to yield the desired product (33.0 mg, 21%).

LC-MS (method 10): R_(t)=2.49 min; MS (ESIpos): m/z=476 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.957 (3.55), 0.976(7.83), 0.995 (3.65), 1.141 (0.50), 1.234 (0.73), 2.220 (3.64), 2.447(0.86), 2.465 (2.45), 2.485 (3.08), 2.652 (16.00), 4.399 (0.63), 4.434(1.14), 4.469 (0.64), 6.214 (0.65), 6.342 (0.62), 6.352 (1.31), 6.361(0.65), 6.489 (0.62), 7.272 (2.06), 7.294 (4.19), 7.316 (2.31), 7.673(1.60), 7.687 (2.04), 7.694 (1.96), 7.708 (1.50), 8.501 (0.91), 9.493(1.33).

Example 1644-[5-({6-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-yl}amino)-1-(cyclopropylmethyl)-4-ethyl-1H-pyrazol-3-yl]benzonitrile

A microwave vial was charged4-chloro-6-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine(125 mg, 448 μmol),4-[5-amino-1-(cyclopropylmethyl)-4-ethyl-1H-pyrazol-3-yl]benzonitrile(131 mg, 493 μmol) and sodium phenolate (78.0 mg, 672 μmol) and thecontents were suspended in 1,4-dioxane (2.5 ml, 29 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (5.33 mg, 5.82 μmol) and Xantphos(7.77 mg, 13.4 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with water and extracted with ethyl acetate(2×). The combined organic phases were dried over Extrelut NT3 andconcentrated under reduced pressure. The crude product was purified byflash chromatography (dichloromethane/ethyl acetate, Biotage SNAP KP-Sil10 g) and subsequent preparative HPLC (method: column: Reprosil C18; 10μm; 125×30 mm/flow: 50 mL/min/solvent: A=water (0.01% formic acid),B=acetonitrile/gradient: 0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75min=100% B, 19.75-23.00 min=90% B) to yield the desired product (37.5mg, 30%).

LC-MS (method 10): R_(t)=2.43 min; MS (ESIpos): m/z=509 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.319 (4.87), 0.449(5.54), 0.468 (5.75), 0.994 (7.41), 1.013 (15.85), 1.032 (7.82), 1.075(1.90), 1.093 (3.76), 1.110 (1.93), 1.184 (0.86), 1.196 (1.56), 1.203(1.56), 1.215 (2.19), 1.232 (1.68), 1.245 (0.84), 2.295 (3.02), 2.372(0.50), 2.684 (0.44), 3.358 (0.69), 3.376 (1.85), 3.393 (1.82), 3.411(0.62), 3.836 (3.89), 3.848 (3.96), 7.318 (0.55), 7.901 (16.00), 7.921(3.86), 8.039 (4.59), 8.170 (2.13), 8.500 (0.79), 9.608 (0.70).

Example 1654-[1-(cyclopropylmethyl)-5-({6-[4-(2-hydroxypropan-2-yl)-3,5-dimethyl-1H-pyrazol-1-yl]pyrimidin-4-yl}amino)-4-methyl-1H-pyrazol-3-yl]benzonitrile

Ethyl1-(6-{[3-(4-cyanophenyl)-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimi-din-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(610 mg, 1.23 mmol) was dissolved in tetrahydrofuran under an argonatmosphere and the resulting solution cooled to 0° C. A solution ofmethylmagnesium bromide (4.9 ml, 1.0 M, 4.9 mmol) was added dropwise andthe reaction mixture allowed to warm to ambient temperature. After 1.5h, another aliquot of methylmagnesium bromide (4.9 ml, 1.0 M, 4.9 mmol)was added and the reaction mixture stirred for another hour. It was thenquenched with cold saturated aqueous ammonium chloride solution andextracted with ethyl acetate (2×). The combined organic phase extractswere dried over sodium sulfate and concentrated. The residue waspurified by flash column chromatography (50 g Snap Ultra,methanol/dichloromethane gradient 1/99 to 5/95) to yield the desiredproduct (278 mg, 47% yield) after concentration of allproduct-containing fractions.

LC-MS (method 11): R_(f)=1.32 min; MS (ESIpos): m/z=483 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.14), 0.008(1.29), 0.306 (1.89), 0.317 (2.10), 0.433 (1.86), 0.453 (1.97), 1.190(0.49), 1.196 (0.48), 1.209 (0.77), 1.220 (0.46), 1.228 (0.47), 1.465(16.00), 2.059 (12.66), 2.073 (0.53), 2.267 (2.33), 2.742 (12.26), 3.859(1.86), 3.876 (1.83), 4.856 (3.35), 7.881 (0.56), 7.904 (10.49), 7.928(0.56), 8.459 (0.57), 9.410 (0.67).

Example 166tert-butyl5-(difluoromethyl)-1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3-methyl-1H-pyrazole-4-carboxylate

A round-bottom flask was charged with4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (1.19 g, 5.42mmol) and sodium phenolate (859 mg, 7.40 mmol) and the contents weresuspended in 1,4-dioxane (12 mL). The reaction mixture was degassed withAr for 3 min. Tris(dibenzylideneacetone)dipalladium (58.7 mg, 64.1μmol), XantPhos (85.6 mg, 148 μmol) and tert-butyl1-(6-chloropyrimidin-4-yl)-5-(difluoromethyl)-3-methyl-1H-pyrazole-4-carboxylate(1.70 g, 4.93 mmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 90° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was filtered, concentrated and purified by flash columnchromatography (Snap Ultra 50 g, gradient cyclohexane/ethyl acetate 95/5to 50:50) to yield the desired product (490 mg, 19% yield).

LC-MS (method 10): R_(t)=2.52 min; MS (ESIpos): m/z=528 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.31), 0.008(0.31), 0.875 (1.16), 0.894 (2.65), 0.913 (1.21), 1.398 (0.46), 1.503(0.18), 1.539 (16.00), 1.560 (0.45), 2.298 (0.25), 2.316 (0.69), 2.334(0.70), 2.353 (0.23), 2.524 (0.26), 2.874 (5.17), 3.639 (5.51), 7.099(0.39), 7.233 (0.83), 7.355 (0.71), 7.360 (0.35), 7.367 (0.47), 7.377(1.56), 7.399 (0.98), 7.421 (0.24), 7.501 (0.89), 7.506 (0.42), 7.514(1.00), 7.522 (0.81), 7.531 (0.33), 7.536 (0.67), 8.579 (0.73), 9.701(0.24).

Example 167N-[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3-methyl-2H-pyrazolo[3,4-b]pyridin-2-yl)pyrimidin-4-amine

A microwave vial was charged with the mixture of1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazolo[3,4-b]pyridine and2-(6-chloropyrimidin-4-yl)-3-methyl-pyrazolo[3,4-b]pyridine (70:30, 185mg, 753 μmol) and sodium phenolate (119 mg, 1.03 mmol) and the contentswere suspended in 1,4-dioxane (2.0 mL). The reaction mixture was degassed with Ar for 3 min.

Tris(dibenzylideneacetone)dipalladium (9.40 mg, 10.3 μmol), XantPhos(11.9 mg, 20.5 μmol) and4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (150 mg, 684μmol) were added and the reaction mixture was degassed again for 1 min.The vial was sealed and heated at 90° C. overnight while vigorouslyshaking. After cooling to ambient temperature, the reaction mixture wasfiltered, diluted with dimethylsulfoxide and purified by preparativeHPLC (column: Chromatorex C18; 125*30 mm, 10 μM, flow 75 mL/min,gradient acetonitrile/water (containing 0.1% trifluoroacetic acid) 10/90to 90/10) and further repurified by preparative HPLC (method 1) to yieldthe desired product (20 mg, 6% yield) along with the regioisomer (56 mg,18% yield).

LC-MS (method 10): R_(t)=2.05 min; MS (ESIpos): m/z=429 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.77), 0.008(0.66), 0.896 (3.29), 0.906 (1.22), 0.914 (7.58), 0.933 (3.37), 2.320(0.86), 2.338 (2.37), 2.357 (2.25), 2.375 (0.73), 2.524 (0.61), 2.608(1.35), 3.019 (15.78), 3.675 (16.00), 7.088 (1.56), 7.099 (1.53), 7.110(1.57), 7.120 (1.65), 7.360 (1.91), 7.366 (0.76), 7.383 (4.27), 7.394(0.73), 7.399 (0.93), 7.405 (2.64), 7.413 (0.48), 7.524 (0.57), 7.531(2.48), 7.536 (1.13), 7.544 (2.70), 7.553 (2.18), 7.561 (0.89), 7.566(1.86), 7.623 (2.10), 8.306 (1.76), 8.311 (1.83), 8.328 (1.73), 8.332(1.72), 8.635 (2.32), 8.679 (1.81), 8.684 (1.76), 8.689 (1.85), 8.694(1.62), 9.693 (1.71).

Example 168N-[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3-methyl-1H-pyrazolo[3,4-c]pyridin-1-yl)pyrimidin-4-amine

A round bottom flask was charged with1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazolo[3,4-c]pyridine (123 mg,502 μmol) and sodium phenolate (79.4 mg, 684 μmol) and the contents weresuspended in 1,4-dioxane (1.3 mL). The reaction mixture was de gassedwith Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (6.26 mg, 6.84μmol), XantPhos (7.92 mg, 13.7 μmol) and4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (100 mg, 456μmol) was added and the reaction mixture was degassed again for 1 min.The vial was sealed and heated at 90° C. overnight while vigorouslystirring. After cooling to ambient temperature, the reaction mixture wasfiltered, diluted with dimethylsulfoxide and purified by preparativeHPLC (method 7) to yield the desired product (38 mg, 17% yield).

LC-MS (method 10): R_(t)=2.09 min; MS (ESIpos): m/z=429 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.91 (t, J=7.4 Hz, 3H),2.35 (q, J=7.4 Hz, 2H), 2.63 (s, 3H), 3.69 (s, 3H), 7.34-7.46 (m, 2H),7.46-7.60 (m, 3H), 7.90 (dd, J=5.36, 1.26 Hz, 1H), 8.47 (d, J=5.36 Hz,1H), 8.61 (s, 1H), 9.48 (s, 1H), 10.08 (s, 1H).

Example 169N-[1-(cyclopropylmethyl)-5-(4-fluorophenyl)-4-methyl-1H-pyrazol-3-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (75.9 mg, 364 μmol),1-(cyclopropylmethyl)-5-(4-fluorophenyl)-4-methyl-1H-pyrazol-3-amine(98.1 mg, 400 μmol) and sodium phenolate (63.3 mg, 545 μmol) and thecontents were suspended in 1,4-dioxane (2.0 ml, 23 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (4.33 mg, 4.73 μmol) and Xantphos(6.31 mg, 10.9 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with saturated sodium bicarbonate solutionand extracted with ethyl acetate (2×). The combined organic phases weredried over Extrelut NT3 and concentrated under reduced pressure. Thecrude product was purified by preparative HPLC (method 8) to yield thedesired product (551. mg, 36%).

LC-MS (method 10): R_(t)=2.58 min; MS (ESIpos): m/z=418 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.213 (3.62), 0.224(3.79), 0.432 (3.59), 0.452 (3.63), 0.464 (0.83), 1.028 (0.45), 1.046(0.87), 1.058 (1.19), 1.070 (0.82), 1.076 (0.82), 1.856 (14.80), 2.173(15.76), 2.631 (16.00), 3.166 (0.41), 3.179 (0.42), 3.807 (5.14), 3.824(5.07), 6.127 (4.26), 7.356 (1.96), 7.378 (4.75), 7.400 (3.07), 7.480(2.87), 7.497 (3.45), 7.514 (2.21), 7.665 (0.71), 8.464 (4.15), 9.453(4.70).

Example 1706-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-[1-(cyclopropylmethyl)-5-(4-fluorophenyl)-4-methyl-1H-pyrazol-3-yl]pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (88.4 mg,364 μmol),1-(cyclopropylmethyl)-5-(4-fluorophenyl)-4-methyl-1H-pyrazol-3-amine(98.1 mg, 400 μmol) and sodium phenolate (63.3 mg, 545 μmol) and thecontents were suspended in 1,4-dioxane (2.0 ml, 23 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (4.33 mg, 4.73 μmol) and Xantphos(6.31 mg, 10.9 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with saturated sodium bicarbonate solutionand extracted with ethyl acetate (2×). The combined organic phases weredried over Extrelut NT3 and concentrated under reduced pressure. Thecrude product was purified by preparative HPLC (method 8) to yield thedesired product (44.7 mg, 27%).

LC-MS (method 9): R_(t)=1.38 min; MS (ESIpos): m/z=452 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.216 (2.25), 0.228(2.38), 0.420 (0.82), 0.434 (2.41), 0.450 (2.43), 0.466 (0.69), 1.036(0.62), 1.042 (0.59), 1.054 (0.92), 1.074 (1.51), 1.091 (2.14), 1.109(1.00), 1.856 (10.75), 2.210 (14.48), 2.229 (0.53), 2.650 (16.00), 2.671(0.69), 3.375 (1.02), 3.392 (0.97), 3.805 (4.22), 3.822 (4.18), 7.356(1.91), 7.378 (4.46), 7.400 (2.89), 7.478 (2.78), 7.492 (3.03), 7.500(2.54), 7.513 (1.96), 8.499 (3.75), 9.580 (2.82).

Example 171N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (75.0 mg, 359 μmol),1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine(97.0 mg, 395 μmol) and sodium phenolate (62.6 mg, 539 μmol) and thecontents were suspended in 1,4-dioxane (1.5 ml, 18 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (4.28 mg, 4.67 μmol) and Xantphos(6.24 mg, 10.8 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with saturated sodium bicarbonate solutionand extracted with ethyl acetate (2×). The combined organic phases weredried over Extrelut NT3 and concentrated under reduced pressure. Thecrude product was purified by preparative HPLC (method 8) to yield thedesired product (33.0 mg, 20%).

LC-MS (method 10): R_(t)=2.26 min; MS (ESIpos): m/z=418 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.41), 0.008(1.27), 0.293 (2.60), 0.305 (2.86), 0.422 (2.63), 0.442 (2.79), 1.178(0.71), 1.185 (0.70), 1.197 (1.08), 1.209 (0.66), 1.216 (0.67), 2.009(16.00), 2.168 (3.50), 2.188 (2.00), 2.629 (15.78), 2.654 (1.04), 3.826(2.61), 3.844 (2.58), 6.141 (3.06), 7.252 (2.74), 7.274 (5.22), 7.297(2.76), 7.383 (0.45), 7.716 (1.62), 7.731 (2.15), 7.736 (2.10), 7.751(1.58), 8.462 (0.78), 9.371 (0.79).

Example 1726-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]-N-[1-(2,2-difluoroethyl)-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]pyrimidin-4-amine

A microwave vial was charged4-chloro-6-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine(94.2 mg, 338 μmol),1-(2,2-difluoroethyl)-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-amine (100mg, 371 μmol) and sodium phenolate (58.8 mg, 506 μmol) and the contentswere suspended in 1,4-dioxane (2.4 ml, 28 mmol). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylidenaceton)dipalladium(4.02 mg, 4.39 μmol) and Xantphos (5.86 mg, 10.1 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously stirring. After coolingto ambient temperature, the reaction mixture was diluted with saturatedsodium bicarbonate solution and extracted with ethyl acetate (2×). Thecombined organic phases were dried over sodium sulfate and concentratedunder reduced pressure. The crude product was purified by preparativeHPLC (method 5) to yield the desired product (82.0 mg, 43%).

LC-MS (method 9): R_(t)=1.30 min; MS (ESIpos): m/z=512 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.66), 0.008(1.10), 0.864 (4.01), 0.883 (8.88), 0.902 (3.94), 2.277 (16.00), 2.308(2.57), 2.327 (2.66), 2.345 (0.88), 2.367 (0.41), 2.519 (1.71), 2.524(1.63), 4.306 (1.11), 4.316 (1.20), 4.343 (2.25), 4.352 (2.20), 4.379(1.11), 4.389 (0.99), 6.150 (0.75), 6.278 (0.74), 6.287 (1.57), 6.296(0.71), 6.424 (0.69), 7.375 (2.15), 7.380 (0.95), 7.397 (5.20), 7.414(1.15), 7.419 (3.34), 7.466 (3.28), 7.472 (1.53), 7.480 (3.63), 7.488(2.50), 7.496 (1.08), 7.502 (2.02), 7.548 (0.54), 7.907 (1.41), 8.038(3.12), 8.170 (1.26), 8.525 (2.96), 9.803 (1.70).

Example 173N-[1-(2,2-difluoroethyl)-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (70.4 mg, 338 μmol),1-(2,2-difluoroethyl)-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-amine (100mg, 371 μmol) and sodium phenolate (58.8 mg, 506 μmol) and the contentswere suspended in 1,4-dioxane (3.8 ml, 45 mmol). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylidenaceton)dipalladium(4.02 mg, 4.39 μmol) and Xantphos (5.86 mg, 10.1 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously stirring. After coolingto ambient temperature, the reaction mixture was diluted with saturatedsodium bicarbonate solution and extracted with ethyl acetate (2×). Thecombined organic phases were dried over sodium sulfate and concentratedunder reduced pressure. The crude product was purified by preparativeHPLC (method 4) to yield the desired product (40.0 mg, 27%).

LC-MS (method 9): R_(t)=1.18 min; MS (ESIpos): m/z=442 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.865 (4.13), 0.884(8.87), 0.902 (4.25), 2.178 (15.81), 2.283 (1.23), 2.301 (3.58), 2.320(3.55), 2.338 (1.22), 2.625 (16.00), 4.296 (1.30), 4.305 (1.38), 4.333(2.65), 4.342 (2.63), 4.369 (1.37), 4.378 (1.25), 6.132 (4.28), 6.147(0.48), 6.157 (0.82), 6.285 (0.80), 6.294 (1.60), 6.303 (0.79), 6.432(0.76), 7.373 (1.81), 7.395 (4.43), 7.417 (2.85), 7.462 (3.30), 7.477(5.09), 7.482 (5.10), 7.496 (2.28), 8.463 (4.38), 9.484 (4.34).

Example 1746-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-[1-(2,2-difluoroethyl)-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (82.1 mg,338 μmol),1-(2,2-difluoroethyl)-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-amine (100mg, 371 μmol) and sodium phenolate (58.8 mg, 506 μmol) and the contentswere suspended in 1,4-dioxane (2.4 ml, 28 mmol). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylidenaceton)dipalladium(4.02 mg, 4.39 μmol) and Xantphos (5.86 mg, 10.1 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously stirring. After coolingto ambient temperature, the reaction mixture was diluted with saturatedsodium bicarbonate solution and extracted with ethyl acetate (2×). Thecombined organic phases were dried over sodium sulfate and concentratedunder reduced pressure. The crude product was purified by preparativeHPLC (method 5) to yield the desired product (57.0 mg, 32%).

LC-MS (method 9): R_(t)=1.32 min; MS (ESIpos): m/z=476 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.865 (3.58), 0.884(8.04), 0.902 (3.74), 2.074 (0.91), 2.215 (15.14), 2.229 (1.33), 2.288(0.97), 2.306 (2.78), 2.325 (2.80), 2.343 (0.89), 2.644 (16.00), 2.670(1.17), 4.299 (1.06), 4.308 (1.14), 4.336 (2.16), 4.345 (2.19), 4.372(1.10), 4.381 (1.01), 6.153 (0.70), 6.281 (0.67), 6.290 (1.41), 6.299(0.68), 6.428 (0.66), 7.374 (1.75), 7.396 (4.45), 7.418 (2.89), 7.463(2.91), 7.477 (3.37), 7.484 (2.68), 7.499 (2.20), 7.513 (1.28), 8.502(4.11), 9.609 (2.90).

Example 1756-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (100 mg,411 μmol),1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine(111 mg, 452 μmol) and sodium phenolate (71.6 mg, 617 μmol) and thecontents were suspended in 1,4-dioxane (2.0 ml, 23 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (4.90 mg, 5.35 μmol) and Xantphos(7.14 mg, 12.3 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with saturated sodium bicarbonate solutionand extracted with ethyl acetate (2×). The combined organic phases weredried over sodium sulfate and concentrated under reduced pressure. Thecrude product was purified by preparative HPLC (method 8) andsubsequently by flash chromatography on silica gel(dichloromethane/ethyl acetate, Biotage, SNAP KP-Sil 10 g) to yield thedesired product (66.3 mg, 35%).

LC-MS (method 10): R_(t)=2.76 min; MS (ESIpos): m/z=452 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.291 (2.59), 0.302(2.80), 0.422 (2.64), 0.442 (2.80), 1.175 (0.72), 1.182 (0.68), 1.194(1.05), 1.205 (0.65), 1.212 (0.68), 2.007 (15.14), 2.207 (2.73), 2.646(16.00), 3.164 (5.16), 3.177 (5.32), 3.827 (2.48), 3.844 (2.43), 4.064(0.60), 4.077 (1.73), 4.090 (1.69), 4.104 (0.56), 7.252 (2.09), 7.274(4.21), 7.296 (2.29), 7.715 (1.54), 7.729 (2.07), 7.749 (1.43), 8.498(0.53), 9.470 (0.46).

Example 1766-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]-N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]pyrimidin-4-amine

A microwave vial was charged4-chloro-6-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine(100 mg, 358 μmol),1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine(96.7 mg, 394 μmol) and sodium phenolate (62.4 mg, 537 μmol) and thecontents were suspended in 1,4-dioxane (2.0 ml, 23 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (4.27 mg, 4.66 μmol) and Xantphos(6.22 mg, 10.7 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with saturated sodium bicarbonate solutionand extracted with ethyl acetate (2×). The combined organic phases weredried over Extrelut NT3 and concentrated under reduced pressure. Thecrude product was purified by preparative HPLC (method 8) to yield thedesired product (20.0 mg, 10%).

LC-MS (method 10): R_(t)=2.46 min; MS (ESIpos): m/z=488 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.290 (2.86), 0.301(3.02), 0.425 (3.09), 0.445 (3.21), 1.161 (0.46), 1.173 (0.86), 1.180(0.83), 1.192 (1.23), 1.204 (0.77), 1.211 (0.81), 1.223 (0.43), 2.010(16.00), 2.279 (1.95), 2.296 (5.48), 3.832 (2.23), 3.847 (2.21), 7.255(2.20), 7.277 (4.56), 7.298 (3.73), 7.327 (0.43), 7.346 (0.70), 7.366(0.53), 7.493 (0.79), 7.512 (1.14), 7.532 (0.55), 7.733 (2.11), 7.863(0.40), 7.904 (1.38), 7.994 (0.76), 8.036 (2.76), 8.167 (1.27), 8.749(1.16).

Example 177 ethyl1-(6-{[1-(2,2-difluoroethyl)-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

A microwave vial was charged ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (94.8mg, 338 μmol),1-(2,2-difluoroethyl)-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-amine (100mg, 371 μmol) and sodium phenolate (58.8 mg, 506 μmol) and the contentswere suspended in 1,4-dioxane (2.4 ml, 28 mmol). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylidenaceton)dipalladium(4.02 mg, 4.39 μmol) and Xantphos (5.86 mg, 10.1 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously stirring. After coolingto ambient temperature, the reaction mixture was diluted with saturatedsodium bicarbonate solution and extracted with ethyl acetate (2×). Thecombined organic phases were dried over sodium sulfate and concentratedunder reduced pressure. The crude product was purified by preparativeHPLC (method 8) and subsequent flash chromatography on silica gel(cyclohexane/ethyl acetate 3:1) to yield the desired product (25.0 mg,14%).

LC-MS (method 10): R_(t)=2.43 min; MS (ESIpos): m/z=514 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.870 (3.77), 0.888(8.24), 0.907 (3.93), 1.074 (0.69), 1.091 (1.39), 1.109 (0.71), 1.290(4.26), 1.308 (8.80), 1.326 (4.37), 2.295 (1.01), 2.313 (2.86), 2.332(2.92), 2.351 (1.02), 2.376 (15.00), 2.899 (16.00), 3.375 (0.70), 3.392(0.70), 4.230 (1.33), 4.248 (4.06), 4.266 (4.03), 4.284 (1.37), 4.297(1.18), 4.307 (1.24), 4.334 (2.32), 4.343 (2.34), 4.370 (1.19), 4.379(1.09), 6.150 (0.73), 6.279 (0.71), 6.288 (1.48), 6.297 (0.73), 6.425(0.69), 7.374 (1.74), 7.396 (4.42), 7.418 (2.89), 7.464 (2.93), 7.477(3.40), 7.484 (2.58), 7.499 (1.91), 7.543 (0.96), 8.550 (3.71), 9.701(2.49).

Example 178 ethyl4-chloro-1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate

A microwave vial was charged ethyl4-chloro-1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate(340 mg, 1.13 mmol),4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (272 mg, 1.24mmol) and sodium phenolate (197 mg, 1.69 mmol) and the contents weresuspended in 1,4-dioxane (10 ml, 120 mmol). The reaction mixture wasdegassed with Ar for 3 min.

Tris(dibenzylidenaceton)dipalladium (13.4 mg, 14.7 μmol) and Xantphos(19.6 mg, 33.9 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with saturated sodium bicarbonate solutionand extracted with ethyl acetate (2×). The combined organic phases weredried over sodium sulfate and concentrated under reduced pressure. Thecrude product was purified by preparative HPLC (method 4) andsubsequently by flash chromatography on silica gel (cyclohexane/ethylacetate 2:1) to yield the desired product (90.0 mg, 16%).

LC-MS (method 10): R_(t)=2.39 min; MS (ESIpos): m/z=484 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.870 (3.65), 0.888(7.93), 0.907 (3.60), 1.227 (4.94), 1.245 (10.13), 1.263 (4.88), 2.258(0.69), 2.278 (15.19), 2.294 (1.12), 2.312 (2.42), 2.331 (2.48), 2.350(0.76), 2.524 (1.25), 3.658 (16.00), 4.322 (1.60), 4.339 (4.83), 4.357(4.76), 4.375 (1.47), 7.313 (1.11), 7.359 (2.08), 7.381 (4.59), 7.403(2.72), 7.505 (2.74), 7.519 (3.04), 7.526 (2.51), 7.540 (2.01), 8.420(2.91), 9.670 (1.25).

Example 1796-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]-N-[1-(2,2-difluoroethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]pyrimidin-4-amine

A microwave vial was charged4-chloro-6-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine(94.2 mg, 338 μmol),1-(2,2-difluoroethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-amine (100mg, 371 μmol) and sodium phenolate (58.8 mg, 506 μmol) and the contentswere suspended in 1,4-dioxane (2.4 ml, 28 mmol). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylidenaceton)dipalladium(4.02 mg, 4.39 μmol) and Xantphos (5.86 mg, 10.1 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously stirring. After coolingto ambient temperature, the reaction mixture was diluted with saturatedsodium bicarbonate solution and extracted with ethyl acetate (2×). Thecombined organic phases were dried over sodium sulfate and concentratedunder reduced pressure. The crude product was purified by preparativeHPLC (method: column: Reprosil C18; 10 μm; 125×40 mm/flow: 75mL/min/solvent: A=water (0.1% formic acid), B=acetonitrile/gradient:0.00-5.50 min=10% B, 17.65-19.48 min=95% B, 19.66 min=10% B) to yieldthe desired product (35.0 mg, 20%).

LC-MS (method 10): R_(t)=2.44 min; MS (ESIpos): m/z=512 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (5.69), 0.008(3.54), 0.146 (0.42), 0.956 (7.47), 0.975 (16.00), 0.994 (7.34), 1.073(1.02), 1.091 (1.97), 1.108 (1.02), 1.234 (0.64), 1.356 (1.66), 2.284(4.46), 2.327 (1.17), 2.366 (0.87), 2.448 (2.06), 2.466 (7.00), 2.524(4.29), 2.670 (0.76), 2.686 (0.42), 2.710 (0.76), 3.357 (0.53), 3.375(1.08), 3.392 (1.04), 4.437 (1.89), 6.205 (0.64), 6.215 (1.21), 6.343(1.25), 6.353 (2.44), 6.362 (1.17), 6.490 (1.17), 6.499 (0.64), 7.274(4.01), 7.296 (7.81), 7.318 (4.24), 7.675 (2.72), 7.689 (3.54), 7.709(2.31), 7.910 (2.53), 8.041 (4.99), 8.173 (2.23), 8.521 (1.08), 9.654(1.15).

Example 180 ethyl1-(6-{[1-(2,2-difluoroethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

A microwave vial was charged ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (94.8mg, 338 μmol),1-(2,2-difluoroethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-amine (100mg, 371 μmol) and sodium phenolate (58.8 mg, 506 μmol) and the contentswere suspended in 1,4-dioxane (2.4 ml, 28 mmol). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylidenaceton)dipalladium(4.02 mg, 4.39 μmol) and Xantphos (5.86 mg, 10.1 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously stirring. After coolingto ambient temperature, the reaction mixture was diluted with saturatedsodium bicarbonate solution and extracted with ethyl acetate (2×). Thecombined organic phases were dried over sodium sulfate and concentratedunder reduced pressure. The crude product was purified by preparativeHPLC (method: column: Reprosil C18; 10 μm; 125×40 mm/flow: 75mL/min/solvent: A=water (0.1% formic acid), B=acetonitrile/gradient:0.00-5.50 min=10% B, 17.65-19.48 min=95% B, 19.66 min=10% B) to yieldthe desired product (85.0 mg, 49%).

LC-MS (method 10): R_(t)=2.38 min; MS (ESIpos): m/z=514 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (3.10), 0.008(2.60), 0.961 (4.24), 0.979 (9.40), 0.998 (4.37), 1.291 (4.40), 1.308(9.07), 1.326 (4.46), 2.073 (1.71), 2.328 (0.71), 2.382 (3.51), 2.450(1.11), 2.469 (3.01), 2.524 (1.73), 2.670 (0.55), 2.710 (0.46), 2.917(16.00), 4.232 (1.28), 4.250 (4.00), 4.268 (3.96), 4.285 (1.30), 4.404(0.70), 4.437 (1.31), 4.471 (0.71), 6.215 (0.79), 6.343 (0.73), 6.353(1.57), 6.362 (0.74), 6.490 (0.74), 7.271 (2.56), 7.293 (5.29), 7.316(2.93), 7.672 (1.91), 7.686 (2.39), 7.693 (2.31), 7.707 (1.79), 8.539(0.93), 9.562 (1.16).

Example 1812-[1-(6-{[4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]propan-2-ol

A solution of ethyl1-(6-{[4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(187 mg, 416 μmol) in tetrahydrofuran (5.6 ml) was treated withbromo(methyl)magnesium (1.9 ml, 1.0 M in tetrahydrofurane, 1.9 mmol) at0° C. The mixture was stirred for 2 h at 0° C. No conversion wasobserved. The mixture was allowed to warm to ambient temperature andadditional 4.5 eq of bromo(methyl)magnesium (1.87 mL, 1.87 mmol, 1.0 Min tetrahydrofuran) were added. The mixture was stirred 2 days atambient temperature. Additional 4.5 eq bromo(methyl)magnesium (0.62 mL,1.87 mmol, 3 M in diethyl ether) were added and stirring was extendedfor 4 days. The mixture was diluted with saturated ammonium chloridesolution and extracted with ethyl acetate. The combined organic phaseswere dried over magnesium sulfate and the solvent was removed underreduced pressure. The crude product was purified by preparative HPLC(method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 20 mL/min/solvent:A=water (0.1% formic acid), B=acetonitrile) to obtain 26.7 mg of thedesired product (14%).

LC-MS (method 10): R_(t)=1.76 min; MS (ESIpos): m/z=436 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.36), 0.008(1.23), 0.995 (1.54), 1.013 (3.40), 1.032 (1.59), 1.466 (16.00), 2.073(1.62), 2.259 (5.60), 2.562 (0.55), 2.722 (4.32), 4.837 (1.85), 7.334(0.66), 7.356 (0.91), 7.378 (0.52), 7.604 (0.78), 8.454 (0.76), 9.325(0.62), 12.792 (0.76).

Example 182N-[1-(cyclobutylmethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (31.2 mg, 150 μmol),1-(cyclobutylmethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-amine (50.0mg, 90% purity, 165 μmol) and sodium phenolate (26.1 mg, 224 μmol) andthe contents were suspended in 1,4-dioxane (1.5 ml, 18 mmol). Thereaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (1.78 mg, 1.95 ttmol) and Xantphos(2.60 mg, 4.49 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with saturated sodium bicarbonate solutionand extracted with ethyl acetate (2×). The combined organic phases werefiltered over an Extrelut column, the solution was concentrated underreduced pressure and the crude product was purified by flashchromatography (method: column: Biotage KP-Sil 10 g; solvent A:dichloromethane (91%) solvent B: ethyl acetate (9%)) to yield thedesired product (19.7 mg, 28%).

LC-MS (method 11): R_(t)=1.63 min; MS (ESIpos): m/z=446 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (1.58), −0.008(13.80), 0.008 (11.10), 0.146 (1.52), 0.859 (0.45), 0.958 (4.11), 0.977(8.90), 0.995 (4.23), 1.766 (4.23), 1.791 (1.63), 1.953 (1.80), 2.167(2.59), 2.210 (2.03), 2.327 (1.52), 2.332 (1.13), 2.366 (2.08), 2.446(2.14), 2.465 (2.37), 2.519 (6.31), 2.524 (5.35), 2.559 (1.35), 2.561(1.13), 2.567 (1.01), 2.575 (0.73), 2.632 (16.00), 2.665 (1.35), 2.670(1.63), 2.674 (1.41), 2.695 (1.92), 2.710 (2.31), 2.724 (0.96), 2.743(1.13), 2.761 (0.90), 3.939 (1.92), 3.955 (1.86), 6.144 (2.48), 7.245(2.42), 7.267 (5.01), 7.289 (2.70), 7.670 (2.03), 7.758 (0.56), 8.458(0.73), 8.881 (0.45), 9.330 (0.62).

Example 183N-[4-chloro-1-(cyclopropylmethyl)-5-(4-fluorophenyl)-1H-pyrazol-3-yl]-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (62.4 mg,257 μmol),4-chloro-1-(cyclopropylmethyl)-5-(4-fluorophenyl)-1H-pyrazol-3-amine(75.0 mg, 282 μmol) and sodium phenolate (44.7 mg, 385 μmol) and thecontents were suspended in 1,4-dioxane (1.5 ml, 18 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (3.05 mg, 3.34 μmol) and Xantphos(4.45 mg, 7.70 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture purified by preparative HPLC (method: column: ReprosilC18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent: A=water (0.01% formicacid), B=acetonitrile/gradient: 0.00-5.00 min=10% B, 6.50 min=20% B,17.0-19.75min=100% B, 19.75-23.00 min=90% B) to yield the desiredproduct (31.1 mg, 26%).

LC-MS (method 10): R_(t)=2.83 min; MS (ESIpos): m/z=472 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.205 (0.70), 0.218(3.02), 0.230 (3.29), 0.242 (0.92), 0.444 (0.88), 0.458 (2.81), 0.477(2.87), 0.490 (0.81), 1.067 (0.71), 1.073 (0.67), 1.086 (1.04), 1.097(0.66), 1.105 (0.69), 2.217 (15.17), 2.652 (16.00), 3.163 (0.58), 3.176(0.60), 3.893 (4.82), 3.911 (4.78), 7.407 (2.10), 7.429 (4.68), 7.451(2.75), 7.504 (1.47), 7.586 (2.68), 7.599 (3.00), 7.607 (2.75), 7.621(2.22), 8.527 (4.17), 9.719 (3.86).

Example 184N-[4-chloro-1-(cyclopropylmethyl)-5-(4-fluorophenyl)-1H-pyrazol-3-yl]-6-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-amine

A microwave vial was charged4-chloro-6-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine(101 mg, 364 μmol),4-chloro-1-(cyclopropylmethyl)-5-(4-fluorophenyl)-1H-pyrazol-3-amine(106 mg, 400 μmol) and sodium phenolate (63.3 mg, 545 μmol) and thecontents were suspended in 1,4-dioxane (2.0 ml, 23 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (4.33 mg, 4.73 μmol) and Xantphos(6.31 mg, 10.9 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with saturated sodium bicarbonate solutionand extracted with ethyl acetate (2×). The combined organic phases weredried over Extrelut NT3 and concentrated under reduced pressure. Thecrude product was purified by preparative HPLC (method 8) to yield thedesired product (22.2 mg, 12%).

LC-MS (method 10): R_(t)=2.74 min; MS (ESIpos): m/z=508 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.88), −0.008(11.34), 0.008 (6.94), 0.146 (0.85), 0.220 (2.48), 0.231 (2.54), 0.449(0.95), 0.459 (2.48), 0.463 (2.48), 0.479 (2.51), 0.495 (0.72), 1.087(1.11), 1.646 (0.42), 2.280 (16.00), 2.327 (1.24), 2.366 (1.14), 2.523(5.83), 2.670 (1.40), 2.710 (1.24), 3.898 (4.76), 3.916 (4.56), 7.409(2.54), 7.431 (5.38), 7.453 (3.10), 7.525 (0.72), 7.589 (3.00), 7.603(3.29), 7.611 (2.77), 7.625 (2.38), 7.911 (1.40), 8.043 (3.13), 8.174(1.27), 8.552 (3.19), 9.924 (2.12).

Example 185

N-[4-chloro-1-(cyclopropylmethyl)-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (62.4 mg,257 μmol),4-chloro-1-(cyclopropylmethyl)-3-(4-fluorophenyl)-1H-pyrazol-5-amine(75.0 mg, 282 μmol) and sodium phenolate (44.7 mg, 385 μmol) and thecontents were suspended in 1,4-dioxane (1.5 ml, 18 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (3.05 mg, 3.34 μmol) and Xantphos(4.45 mg, 7.70 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with saturated sodium bicarbonate solutionand extracted with ethyl acetate (2×). The combined organic phases weredried over Extrelut NT3 and concentrated under reduced pressure. Thecrude product was purified by preparative HPLC (method 8) to yield thedesired product (25.8 mg, 21%).

LC-MS (method 10): R_(t)=2.71 min; MS (ESIpos): m/z=472 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.59), −0.008(5.23), 0.008 (4.70), 0.146 (0.53), 0.310 (0.59), 0.322 (2.49), 0.335(2.68), 0.347 (0.81), 0.455 (2.19), 0.475 (2.34), 1.225 (0.91), 2.091(1.17), 2.222 (7.10), 2.328 (0.85), 2.366 (0.89), 2.523 (2.63), 2.651(16.00), 2.670 (1.10), 2.710 (0.93), 3.891 (2.89), 3.908 (2.80), 7.307(2.12), 7.329 (4.40), 7.351 (2.36), 7.896 (1.91), 7.909 (2.19), 7.918(2.21), 7.931 (1.89), 8.513 (1.44).

Example 186

N-[4-chloro-1-(cyclopropylmethyl)-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-6-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-amine

A microwave vial was charged4-chloro-6-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine(71.6 mg, 257 μmol),4-chloro-1-(cyclopropylmethyl)-3-(4-fluorophenyl)-1H-pyrazol-5-amine(75.0 mg, 282 μmol) and sodium phenolate (44.7 mg, 385 μmol) and thecontents were suspended in 1,4-dioxane (1.5 ml, 18 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (3.05 mg, 3.34 μmol) and Xantphos(4.45 mg, 7.70 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with saturated sodium bicarbonate solutionand extracted with ethyl acetate (2×). The combined organic phases weredried over Extrelut NT3 and concentrated under reduced pressure. Thecrude product was purified by preparative HPLC (method 8) to yield thedesired product (10.7 mg, 7%).

LC-MS (method 9): R_(t)=1.38 min; MS (ESIpos): m/z=508 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.150 (0.81), −0.008(7.88), 0.008 (6.26), 0.146 (0.87), 0.310 (1.99), 0.323 (8.19), 0.335(9.40), 0.347 (3.21), 0.460 (7.78), 0.480 (8.25), 1.194 (1.12), 1.207(2.09), 1.214 (1.99), 1.226 (3.18), 1.237 (2.43), 1.244 (2.15), 1.647(2.52), 2.184 (0.50), 2.288 (16.00), 2.295 (15.84), 2.327 (1.68), 2.366(1.49), 2.636 (0.50), 2.670 (1.21), 2.688 (0.65), 2.710 (1.28), 2.994(0.47), 3.900 (7.60), 3.917 (7.50), 3.938 (1.34), 3.955 (1.00), 5.754(0.65), 6.833 (1.43), 7.193 (1.12), 7.219 (1.40), 7.241 (1.87), 7.267(2.65), 7.286 (2.99), 7.296 (3.18), 7.311 (7.25), 7.333 (14.13), 7.355(8.00), 7.365 (3.49), 7.384 (2.86), 7.396 (2.96), 7.437 (1.28), 7.492(2.27), 7.511 (2.43), 7.531 (1.49), 7.823 (0.62), 7.861 (1.31), 7.898(9.31), 7.911 (7.04), 7.919 (6.69), 7.933 (5.45), 7.993 (1.74), 8.030(7.88), 8.044 (0.81), 8.124 (0.81), 8.161 (3.55), 8.553 (3.30), 8.591(0.96), 8.749 (1.93), 9.827 (0.65), 9.902 (1.96).

Example 187N-[4-chloro-1-(cyclopropylmethyl)-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (58.0 mg, 278 μmol),4-chloro-1-(cyclopropylmethyl)-3-(4-fluorophenyl)-1H-pyrazol-5-amine(81.2 mg, 306 μmol) and sodium phenolate (48.4 mg, 417 μmol) and thecontents were suspended in 1,4-dioxane (1.2 ml, 14 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (3.31 mg, 3.61 μmol) and Xantphos(4.82 mg, 8.34 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with saturated sodium bicarbonate solutionand extracted with ethyl acetate (2×). The combined organic phases weredried over Extrelut NT3 and concentrated under reduced pressure. Thecrude product was purified by preparative HPLC (method 8) to yield thedesired product (12.5 mg, 10%).

LC-MS (method 10): R_(t)=2.46 min; MS (ESIpos): m/z=438 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.68), −0.008(6.01), 0.146 (0.66), 0.324 (2.94), 0.339 (3.35), 0.350 (1.01), 0.447(0.91), 0.457 (2.59), 0.477 (2.81), 1.030 (0.58), 1.045 (0.51), 1.229(1.22), 1.647 (0.58), 2.081 (1.06), 2.183 (9.69), 2.327 (0.91), 2.366(0.91), 2.634 (16.00), 2.670 (1.09), 2.710 (1.01), 3.892 (3.58), 3.910(3.63), 6.157 (4.21), 7.307 (2.71), 7.330 (5.55), 7.352 (2.92), 7.398(0.58), 7.898 (2.48), 7.912 (2.87), 7.920 (2.79), 7.934 (2.38), 8.483(2.54).

Example 1882-[1-(6-{[1-(cyclopropylmethyl)-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]propan-2-ol

A solution of ethyl1-(6-{[1-(cyclopropylmethyl)-4-ethyl-5-(4-fluorophenyl)-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(69.0 mg, 137 μmol) in tetrahydrofuran (2.8 ml, 35 mmol) was treatedwith methyllithium (300 μl, 1.6 M in diethyl ether, 480 μmol) at 0° C.The mixture was stirred for 30 minutes at 0° C. The mixture was dilutedwith aqueous saturated ammonium chloride solution and extracted withethyl acetate (3×). The combined organic phases were dried overmagnesium sulfate and concentrated under reduced pressure. The crudeproduct was purified using preparative HPLC (method 3) to yield 20.0 mg(28%) of the desired product.

LC-MS (method 10): R_(t)=2.19 min; MS (ESIpos): m/z=490 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.11), 0.008(0.71), 0.181 (1.34), 0.195 (1.41), 0.207 (0.47), 0.406 (0.52), 0.417(1.25), 0.420 (1.29), 0.426 (0.73), 0.437 (1.37), 0.440 (1.23), 0.452(0.50), 0.870 (2.05), 0.888 (4.44), 0.907 (1.98), 1.044 (0.55), 1.470(16.00), 1.982 (0.57), 2.167 (0.74), 2.263 (7.01), 2.287 (0.58), 2.305(1.36), 2.324 (1.39), 2.343 (0.43), 2.524 (0.62), 2.592 (0.78), 2.732(7.92), 3.094 (0.73), 3.751 (2.13), 3.768 (2.07), 7.352 (1.07), 7.374(2.51), 7.396 (1.55), 7.463 (1.50), 7.469 (0.86), 7.477 (1.70), 7.484(1.36), 7.493 (0.58), 7.499 (1.08), 8.461 (1.95), 9.405 (1.33).

Example 1893-(3-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-1,4-dimethyl-1H-pyrazol-5-yl)benzonitrile

N-(1,4-dimethyl-1H-pyrazol-3-yl)-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine(100 mg, 353 μmol), 3-bromobenzonitrile (106 mg, 582 μmol) and potassiumacetate (72.7 mg, 741 μmol) were suspended in DMA and degassed withargon for 3 min. 1,4-bis(diphenylphosphino)butane-η3-allyl-palladium(II)chloride was then added and the reaction mixture was degassed again for1 min. The vial was sealed and heated at 150° C. overnight whilevigorously shaking. The mixture was diluted with dimethylsulfoxide,filtered and purified by preparative HPLC (method 7) to yield an impureproduct fraction that was further purified by preparative HPLC (Luna 5μC18 100×21.2 mm, flow: 25 mL/min, water(containing 0.1% formicacid)/acetonitrile gradient 0-1 min 98/2; 1-10 min 98/2 to 40/60; 10-12min 40/60 to 5/95; 12-18 min 5/95) to yield the desired product (1.6 mg,1% yield).

LC-MS (method 10): R_(t)=1.95 min; MS (ESIpos): m/z=385 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.875 (13.21), 2.187(15.08), 2.521 (0.40), 2.525 (0.40), 2.624 (13.74), 2.995 (2.11), 3.724(16.00), 6.134 (3.95), 7.387 (1.56), 7.738 (1.13), 7.753 (2.77), 7.769(1.87), 7.823 (1.98), 7.839 (1.33), 7.947 (1.86), 7.963 (1.61), 8.016(3.12), 8.452 (3.77), 9.419 (2.80).

Example 1902-[5-(difluoromethyl)-1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3-methyl-1H-pyrazol-4-yl]propan-2-ol

Tert-butyl5-(difluoromethyl)-1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3-methyl-1H-pyrazole-4-carboxylate(200 mg, 379 μmol) was dissolved in diethylether (4.6 mL) and theresulting solution cooled to 0° C. A solution of methyllithium (1.6 M indiethylether, 950 μl, 1.5 mmol) added dropwise and the reaction mixturestirred at 0° C. for 3 h and overnight at ambient temperature. Thereaction mixture was quenched by addition of water and extracted withethyl acetate (3×). The combined organic phase extracts were dried overmagnesium sulfate and concentrated. The residue was purified bypreparative HPLC (column: Chromatorex C18; 250*30 mm, 10 μM, flow 100mL/min, gradient acetonitrile/water (containing 0.1% trifluoroaceticacid) 10/90 to 95/5) to yield an impure product fraction that wasrepurified on preparative HPLC (method 3) to yield the desired product(5 mg, 2% yield).

LC-MS (method 9): R_(t)=1.07 min; MS (ESIpos): m/z=486 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (2.07), 0.008(1.75), 0.876 (2.69), 0.895 (5.58), 0.914 (2.57), 1.430 (0.86), 1.497(1.75), 1.509 (16.00), 1.545 (0.68), 1.555 (1.03), 2.295 (0.64), 2.314(1.62), 2.332 (1.86), 2.388 (0.40), 2.524 (1.10), 2.601 (2.81), 2.665(8.83), 2.822 (0.69), 3.633 (10.31), 3.642 (3.50), 3.649 (1.33), 3.661(0.98), 5.081 (0.46), 5.096 (0.47), 5.268 (2.90), 7.178 (0.58), 7.262(0.42), 7.314 (1.38), 7.353 (1.77), 7.358 (1.34), 7.375 (3.20), 7.380(2.03), 7.397 (2.16), 7.451 (0.67), 7.499 (1.87), 7.512 (2.16), 7.520(1.90), 7.534 (1.56), 8.534 (1.69), 9.577 (0.65).

Example 1916-(4-bromo-3,5-dimethyl-1H-pyrazol-1-yl)-N-[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]pyrimidin-4-amine

A microwave vial was charged with4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (178 mg, 814μmol), 4-(4-bromo-3,5-dimethyl-1H-pyrazol-1-yl)-6-chloropyrimidine (213mg, 740 μmol) and sodium phenolate (112 mg, 962 μmol) the contents weresuspended in 1,4-dioxane (2.1 mL). The reaction mixture was degassedwith Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (8.81 mg, 9.62μmol) and XantPhos (12.8 mg, 22.2 μmol) were added and the reactionmixture was degassed again for 1 min. The vial was sealed and heated at85° C. overnight while vigorously shaking. After cooling to ambienttemperature, the reaction mixture was diluted with water and extractedwith ethyl acetate. The organic phase extract was dried over sodiumsulfate and concentrated. The residue was purified by flash columnchromatography (SNAP Ultra 10 g, cyclohexane/ethyl acetate gradient88/12 to 0/100) to yield the desired product (193 mg, 50% yield).

LC-MS (method 10): R_(t)=2.50 min; MS (ESIpos): m/z=470 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.90 (s, 3H), 1.51 (s,3H), 2.28-2.38 (m, 2H), 2.67 (s, 3H), 3.63 (s, 3H), 7.26-7.45 (m, 3H),7.45-7.60 (m, 2H), 8.53 (s, 1H), 9.47-9.66 (br s, 1H).

Example 192 tert-butyl1-(6-{[3-(4-cyanophenyl)-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-5-(difluoromethyl)-3-methyl-1H-pyrazole-4-carboxylate

A microwave vial was charged with4-[5-amino-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(200 mg, 793 μmol) and sodium phenolate (125 mg, 1.08 mmol) and thecontents were suspended in 1,4-dioxane (2.0 mL). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium(8.58 mg, 9.37 μmol), XantPhos (12.5 mg, 21.6 μmol) and tert-butyl1-(6-chloropyrimidin-4-yl)-5-(difluoromethyl)-3-methyl-1H-pyrazole-4-carboxylate (248 mg, 721 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously shaking. After cooling to ambient temperature, thereaction mixture was filtered and concentrated. The residue wasredissolved in dimethylsulfoxide and purified by preparative HPLC(method 5) to yield the desired product (34 mg,70% purity, 6% yield).

LC-MS (method 10): R_(t)=2.54 min; MS (ESIpos): m/z=561 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.72), 0.008(0.73), 1.543 (16.00), 2.065 (2.17), 2.911 (5.09), 7.237 (0.81), 7.281(0.90), 7.300 (1.07), 7.303 (0.93), 7.343 (0.63), 7.362 (0.45), 7.371(1.46), 7.491 (0.78), 7.511 (1.04), 7.530 (0.53), 7.903 (2.87), 8.827(0.94).

Example 193 tert-butyl1-(6-{[1-(cyclopropylmethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-5-(difluoromethyl)-3-methyl-1H-pyrazole-4-carboxylate

A microwave vial was charged with1-(cyclopropylmethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-amine (200mg, 771 μmol) and sodium phenolate (122 mg, 1.05 mmol) and the contentswere suspended in 1,4-dioxane (2.0 mL). The reaction mixture wasdegassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (8.35mg, 9.11 μmol), XantPhos (12.2 mg, 21.0 μmol) and tert-butyl1-(6-chloropyrimidin-4-yl)-5-(difluoromethyl)-3-methyl-1H-pyrazole-4-carboxylate(242 mg, 701 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 90° C. overnightwhile vigorously shaking. After cooling to ambient temperature, thereaction mixture was filtered and concentrated. The residue wasredissolved in dimethylsulfoxide and purified by preparative HPLC(method 5) to yield the desired product (40 mg, 10% yield).

LC-MS (method 9): R_(t)=1.38 min; MS (ESIpos): m/z=567 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.25), −0.008(2.00), 0.008 (1.74), 0.146 (0.24), 0.299 (1.57), 0.310 (1.71), 0.439(1.71), 0.458 (1.82), 0.972 (3.02), 0.991 (6.75), 1.009 (3.15), 1.061(0.18), 1.209 (0.74), 1.538 (16.00), 2.328 (0.32), 2.367 (0.41), 2.440(0.66), 2.459 (1.72), 2.477 (1.85), 2.524 (0.85), 2.670 (0.33), 2.710(0.37), 2.905 (2.64), 3.799 (1.27), 3.814 (1.26), 7.251 (2.05), 7.274(4.04), 7.296 (2.25), 7.371 (0.27), 7.662 (1.25), 7.676 (1.55), 7.697(1.09), 8.548 (0.28), 9.569 (0.25).

Example 1946-(3,5-dimethyl-1H-pyrazol-1-yl)-N-[5-(4-fluorophenyl)-1-methyl-4-(pyrrolidin-1-ylmethyl)-1H-pyrazol-3-yl]pyrimidin-4-amine

3-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-5-(4-fluorophenyl)-1-methyl-1H-pyrazole-4-carbaldehyde(50.0 mg, 128 μmol) and pyrrolidine (13 μl, 150 μmol) were dissolved intetrahydrofuran (2.0 mL) and acetic acid (22 μl, 380 μmol) and sodiumtriacetoxyborohydride (32.5 mg, 153 μmol) were added. The reactionmixture was allowed to stirred overnight at ambient temperature. It wasthen quenched with water and extracted with ethyl acetate (3X). Thecombined organic phase extracts were dried over sodium sulfate andconcentrated. The residue was purified by preparative HPLC ( ) to yieldthe desired product (5 mg, 8% yield) after lyophilisation ofproduct-containing fractions.

LC-MS (method 10): R_(t)=1.27 min; MS (ESIpos): m/z=447 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (2.41), 0.008(2.16), 1.753 (3.85), 1.891 (0.75), 2.192 (1.25), 2.208 (16.00), 2.252(1.23), 2.260 (1.13), 2.328 (0.40), 2.367 (0.51), 2.460 (0.93), 2.643(13.78), 2.670 (1.43), 2.710 (0.59), 3.271 (1.16), 3.283 (1.15), 3.735(1.00), 4.204 (3.06), 4.216 (3.02), 4.464 (0.62), 4.727 (0.82), 4.783(0.56), 4.794 (0.55), 6.168 (3.90), 7.422 (2.04), 7.444 (4.33), 7.466(2.44), 7.617 (2.40), 7.631 (2.74), 7.639 (2.41), 7.652 (2.02), 7.890(1.15), 8.550 (4.35), 9.675 (0.46), 9.886 (3.36).

Example 1952-[4-chloro-1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3-methyl-1H-pyrazol-5-yl]propan-2-ol

A solution of ethyl4-chloro-1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate(77.0 mg, 159 μmol) in tetrahydrofuran (3.0 ml, 37 mmol) was treatedwith bromo(methyl)magnesium (560 μl, 1.0 M in tetrahydrofuran, 560 μmol)at 0° C. The mixture was stirred 30 minutes at 0° C. and one hour atambient temperature. Another 2 equivalents of bromo(methyl)magnesium(0.32 mL, 0.32 mmol, 1.0 M in tetrahydrofuran) were added at 0° C. andit was stirred for 30 minutes at 0° C. The mixture was diluted withsaturated ammonia chloride solution and extracted with ethyl acetate(3×). The combined organic phases were dried over magnesium sulfate andconcentrated under reduced pressure. The crude product was purifiedusing flash chromatography (cyclohexane/ethyl acetate) yielding 24.7 mg(30%) of the desired product.

LC-MS (method 9): R_(t)=1.21 min; MS (ESIpos): m/z=470 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.16), 0.008(1.02), 0.875 (2.13), 0.894 (4.95), 0.912 (2.18), 1.356 (1.29), 1.596(16.00), 2.185 (9.41), 2.300 (0.43), 2.318 (1.32), 2.337 (1.29), 2.356(0.41), 2.519 (0.82), 2.524 (0.62), 3.637 (10.54), 6.810 (0.43), 7.275(0.41), 7.355 (1.23), 7.360 (0.48), 7.377 (2.84), 7.394 (0.55), 7.399(1.71), 7.494 (1.63), 7.499 (0.70), 7.507 (1.83), 7.515 (1.45), 7.524(0.59), 7.529 (1.24), 8.535 (1.63), 9.717 (0.55).

Example 1964-(3-{[6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-1,4-dimethyl-1H-pyrazol-5-yl)benzonitrile

A microwave vial was charged with4-(3-amino-1,4-dimethyl-1H-pyrazol-5-yl)benzonitrile (60.0 mg, 283μmol), 4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine(75.6 mg, 311 μmol) and sodium phenolate (36.1 mg, 311 μmol) and thecontents were suspended in 1,4-dioxane (0.9 mL). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium(3.88 mg, 4.24 μmol) and XantPhos (4.91 mg, 8.48 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously shaking. After coolingto ambient temperature, the reaction mixture was filtered andconcentrated. The residue was redissolved in dimethylsulfoxide andpurified by preparative HPLC (method 6) to yield the desired product (31mg, 26% yield).

LC-MS(method 10): R_(t)=2.23 min; MS (ESIpos): m/z=419 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (2.52), 1.647(0.86), 1.887 (13.10), 2.224 (14.65), 2.641 (15.76), 2.679 (0.41), 3.736(16.00), 7.368 (0.65), 7.384 (0.76), 7.398 (1.04), 7.412 (1.31), 7.698(4.17), 7.719 (4.86), 8.004 (4.63), 8.025 (4.11), 8.488 (2.85), 9.550(2.26).

Example 1974-(5-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-1,4-dimethyl-1H-pyrazol-3-yl)benzonitrile

A microwave vial was charged with4-(5-amino-1,4-dimethyl-1H-pyrazol-3-yl)benzonitrile (80.0 mg, 377μmol), 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (86.5 mg, 415μmol) and sodium phenolate (48.1 mg, 415 μmol) and the contents weresuspended in 1,4-dioxane (1.2 mL). The reaction mixture was degassedwith Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (5.18 mg, 5.65μmol) and XantPhos (6.54 mg, 11.3 μmol) were added and the reactionmixture was degassed again for 1 min. The vial was sealed and heated at85° C. overnight while vigorously shaking. After cooling to ambienttemperature, the reaction mixture was filtered and concentrated. Theresidue was redissolved in dimethylsulfoxide and purified by preparativeHPLC (method 1) to yield the desired product (32 mg, 21% yield).

LC-MS (method 11): R_(t)=1.33 min; MS (ESIneg): m/z=383 [M−H]⁻

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (2.46), 0.008(2.56), 2.073 (14.45), 2.177 (3.63), 2.228 (0.43), 2.523 (0.74), 2.631(11.90), 2.665 (0.48), 3.695 (9.97), 6.150 (2.50), 7.897 (16.00), 8.471(0.77), 9.457 (1.59).

Example 1984-[1-(2-cyclopropylethyl)-5-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-4-methyl-1H-pyrazol-3-yl]benzonitrile

A microwave vial was charged with4-[5-amino-1-(2-cyclopropylethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(51.5 mg, 193 μmol), 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine(44.4 mg, 213 μmol) and sodium phenolate (24.7 mg, 213 μmol) and thecontents were suspended in 1,4-dioxane (0.6 mL). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium(2.66 mg, 2.90 μmol) and XantPhos (3.36 mg, 5.80 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously shaking. After coolingto ambient temperature, the reaction mixture was filtered andconcentrated. The residue was redissolved in dimethylsulfoxide andpurified by preparative HPLC (method 6) to yield the desired product(5.9 mg, 7% yield).

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.063 (2.98), −0.054(3.01), −0.051 (2.85), −0.008 (2.13), 0.008 (2.08), 0.309 (1.97), 0.327(2.14), 0.608 (0.62), 0.626 (0.88), 0.645 (0.56), 1.633 (0.94), 1.651(2.67), 1.668 (2.68), 1.686 (0.96), 2.062 (16.00), 2.168 (2.74), 2.524(0.73), 2.630 (14.20), 2.675 (0.41), 4.021 (1.18), 4.038 (2.06), 4.055(1.15), 6.146 (2.73), 7.875 (0.89), 7.897 (11.21), 7.923 (0.83), 8.465(0.75), 9.413 (0.84).

Example 1994-(4-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-3,5-dimethyl-1H-pyrazol-1-yl)benzonitrile

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (89.4 mg, 428 μmol),4-(4-amino-3,5-dimethyl-1H-pyrazol-1-yl)benzonitrile (100 mg, 471 μmol)and sodium phenolate (74.6 mg, 642 μmol) and the contents were suspendedin 1,4-dioxane (3.1 ml, 36 mmol). The reaction mixture was degassed withAr for 3 min. Tris(dibenzylidenaceton)dipalladium (5.10 mg, 5.57 μmol)and Xantphos (7.43 mg, 12.8 μmol) were added and the reaction mixturewas degassed again for 1 min. The vial was sealed and heated at 85° C.overnight while vigorously shaking. After cooling to ambienttemperature, the reaction mixture was purified by preparative HPLC(method: column: Reprosil C18; 10 μm; 125×40 mm/flow: 75 mL/min/solvent:A=water (0.1% formic acid), B=acetonitrile/gradient: 0.00-5.50 min=10%B, 17.65-19.48 min=95% B, 19.66 min=10% B) to yield the desired product(47.0 mg, 28%).

LC-MS (method 10): R_(t)=1.86 min; MS (ESIpos): m/z=385 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.073 (2.04), 2.104(16.00), 2.168 (2.41), 2.294 (11.75), 2.328 (0.44), 2.367 (0.41), 2.616(13.94), 2.670 (0.42), 6.122 (2.44), 7.811 (2.06), 7.832 (2.58), 7.979(4.02), 8.000 (3.21), 8.403 (0.55), 8.931 (3.32).

Example 2004-[4-({6-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-yl}amino)-3,5-dimethyl-1H-pyrazol-1-yl]benzonitrile

A microwave vial was charged4-chloro-6-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine(120 mg, 428 μmol), 4-(4-amino-3,5-dimethyl-1H-pyrazol-1-yl)benzonitrile(100 mg, 471 μmol) and sodium phenolate (54.7 mg, 471 μmol) and thecontents were suspended in 1,4-dioxane (3.1 ml, 36 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (5.10 mg, 5.57 μmol) and Xantphos(7.43 mg, 12.8 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was purified by preparative HPLC (method: column:Reprosil C18; 10 μm; 125×40 mm/flow: 75 mL/min/solvent: A=water (0.1%formic acid), B=acetonitrile/gradient: 0.00-5.50 min=10% B, 17.65-19.48min=95% B, 19.66 min=10% B) to yield the desired product (90.0 mg, 44%).

LC-MS (method 10): R_(t)=2.17 min; MS (ESIpos): m/z=455 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (3.25), 0.008(2.00), 2.073 (13.13), 2.086 (0.74), 2.106 (16.00), 2.292 (10.62), 2.327(1.09), 2.367 (0.45), 2.524 (1.66), 2.670 (0.44), 7.827 (1.54), 7.901(0.73), 7.983 (2.69), 8.004 (2.19), 8.033 (1.49), 8.165 (0.66), 9.208(0.60).

Example 2014-(5-{[6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-1,4-dimethyl-1H-pyrazol-3-yl)benzonitrile

A microwave vial was charged with4-(5-amino-1,4-dimethyl-1H-pyrazol-3-yl)benzonitrile (80.0 mg, 377μmol), 4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (101mg, 415 μmol) and sodium phenolate (48.1 mg, 415 μmol) and the contentswere suspended in 1,4-dioxane (1.2 mL). The reaction mixture wasdegassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (5.18mg, 5.65 μmol) and XantPhos (6.54 mg, 11.3 μmol) were added and thereaction mixture was degassed again for 1 min. The vial was sealed andheated at 85° C. overnight while vigorously shaking. After cooling toambient temperature, the reaction mixture was filtered and concentrated.The residue was redissolved in dimethylsulfoxide and purified bypreparative HPLC (method 6) to yield the desired product (52.8 mg, 33%yield).

LC-MS (method 10): R_(t)=2.27 min; MS (ESIpos): m/z=419 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (3.02), 0.008(1.55), 2.071 (14.95), 2.216 (3.05), 2.266 (0.57), 2.649 (14.46), 2.679(0.58), 3.696 (8.98), 7.896 (16.00), 8.505 (0.65), 9.555 (0.69).

Example 2024-[5-{[6-(4-acetyl-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-1-(cyclopropylmethyl)-4-ethyl-1H-pyrazol-3-yl]benzonitrile

A solution of ethyl1-(6-{[3-(4-cyanophenyl)-1-(cyclopropylmethyl)-4-ethyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(108 mg, 212 μmol) in tetrahydrofuran (2.5 ml, 31 mmol) was treated at0° C. with bromo(methyl)magnesium (250 μl, 3.0 M in diethyl ether, 740μmol). The mixture was stirred overnight at ambient temperature. Twofurther equivalents of bromo(methyl)magnesium (141 μL, 0.42 mmol, 3.0 Min diethyl ether) were added and it was stirred overnight. The mixturewas diluted with water and purified by preparative HPLC (method: column:Reprosil C18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent: A=water (0.01%formic acid), B=acetonitrile/gradient: 0.00-5.00 min=10% B, 6.50 min=20%B, 17.0-19.75 min=100% B, 19.75-23.00 min=90% B) to yield 12.4 mg (12%)of the desired product.

LC-MS (method 11): R_(t)=1.41 min; MS (ESIpos): m/z=481 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.93), −0.008(7.98), 0.008 (7.34), 0.146 (0.88), 0.308 (4.99), 0.446 (5.28), 0.465(5.09), 0.960 (2.69), 0.979 (6.07), 0.993 (7.34), 1.012 (14.73), 1.030(7.73), 1.199 (1.76), 1.217 (2.06), 1.234 (1.86), 2.328 (1.81), 2.366(2.30), 2.466 (13.60), 2.670 (2.06), 2.710 (2.20), 2.893 (16.00), 3.793(2.01), 3.811 (2.25), 3.833 (3.72), 3.850 (3.67), 7.178 (1.22), 7.197(1.42), 7.267 (1.37), 7.286 (0.93), 7.428 (1.17), 7.448 (1.81), 7.467(0.93), 7.830 (2.06), 7.851 (4.94), 7.864 (2.45), 7.885 (12.92), 7.898(15.12), 7.919 (3.47), 8.151 (0.93), 8.245 (1.17), 8.535 (0.73), 9.266(0.54), 9.550 (0.69).

Example 2034-[1-(cyclopropylmethyl)-4-ethyl-5-{[6-(3-methyl-1H-pyrazolo[3,4-c]pyridin-1-yl)pyrimidin-4-yl]amino}-1H-pyrazol-3-yl]benzonitrile

A microwave vial was charged1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazolo[3,4-c]pyridine (100 mg,407 μmol),4-[5-amino-1-(cyclopropylmethyl)-4-ethyl-1H-pyrazol-3-yl]benzonitrile(119 mg, 448 μmol) and sodium phenolate (61.4 mg, 529 μmol) and thecontents were suspended in 1,4-dioxane (2.5 ml, 29 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (4.85 mg, 5.29 μmol) and Xantphos(7.07 mg, 12.2 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was purified by preparative HPLC (method: column:Reprosil C18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent: A=water (0.01%formic acid), B=acetonitrile/gradient: 0.00-5.00 min=10% B, 6.50 min=20%B, 17.0-19.75 min=100% B, 19.75-23.00 min=90% B) and subsequently byflash-chromatography on silica gel (column: SNAP KP-Sil 10 g,dichloromethane/ethyl acetate) to yield the desired product (30.2 mg,16%).

LC-MS (method 10): R_(t)=2.03 min; MS (ESIpos): m/z=476 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (2.92), 0.008(2.70), 0.324 (3.25), 0.334 (3.42), 0.451 (3.52), 0.471 (3.66), 1.016(5.28), 1.035 (11.35), 1.053 (5.44), 1.158 (1.12), 1.176 (2.26), 1.194(1.24), 1.208 (0.59), 1.220 (1.08), 1.238 (1.68), 1.257 (1.03), 1.990(4.08), 2.568 (3.24), 2.587 (2.08), 2.618 (2.89), 2.712 (0.48), 3.863(2.82), 3.878 (2.82), 4.022 (0.99), 4.039 (0.96), 7.911 (16.00), 8.475(4.31), 8.488 (4.14), 8.625 (0.67), 9.509 (0.59), 10.037 (5.68).

Example 204N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-(3-methyl-1H-pyrazolo[3,4-c]pyridin-1-yl)pyrimidin-4-amine

A microwave vial was charged1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazolo[3,4-c]pyridine (100 mg,407 μmol),1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine(110 mg, 448 μmol) and sodium phenolate (61.4 mg, 529 μmol) and thecontents were suspended in 1,4-dioxane (2.5 ml, 29 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (4.85 mg, 5.29 μmol) and Xantphos(7.07 mg, 12.2 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was purified by preparative HPLC (method: column:Reprosil C18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent: A=water (0.01%formic acid), B=acetonitrile/gradient: 0.00-5.00 min=10% B, 6.50 min=20%B, 17.0-19.75 min=100% B, 19.75-23.00 min=90% B) and subsequently byflash-chromatography on silica gel (column: SNAP KP-Sil 10 g, SCM/ethylacetate) to yield the desired product (31.3 mg, 17%).

LC-MS (method 10): R_(t)=2.05 min; MS (ESIpos): m/z=455 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.307 (2.86), 0.319(3.14), 0.430 (2.85), 0.450 (3.06), 0.822 (0.50), 1.176 (0.62), 1.188(0.47), 1.194 (0.59), 1.200 (0.83), 1.207 (0.80), 1.219 (1.27), 1.231(1.12), 1.237 (1.00), 1.249 (0.59), 1.286 (0.49), 1.301 (0.45), 1.990(1.01), 2.042 (16.00), 2.565 (0.48), 2.615 (3.22), 2.672 (0.47), 3.860(2.66), 3.877 (2.62), 5.756 (0.97), 7.265 (2.23), 7.288 (4.50), 7.310(2.53), 7.755 (2.10), 7.892 (1.82), 7.905 (2.06), 8.473 (3.37), 8.486(3.29), 8.633 (0.57), 9.499 (0.59), 10.042 (4.09).

Example 205N-[1-(cyclopropylmethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-6-(3-methyl-1H-pyrazolo[3,4-c]pyridin-1-yl)pyrimidin-4-amine

A microwave vial was charged1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazolo[3,4-c]pyridine (100 mg,407 μmol),1-(cyclopropylmethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-amine (116mg, 448 μmol) and sodium phenolate (61.4 mg, 529 μmol) and the contentswere suspended in 1,4-dioxane (2.5 ml, 29 mmol). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylidenaceton)dipalladium(4.85 mg, 5.29 μmol) and Xantphos (7.07 mg, 12.2 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously stirring. After coolingto ambient temperature, the reaction mixture was diluted with water andextracted with ethyl acetate (2×). The combined organic phases weredried over Extrelut NT3 and concentrated under reduced pressure. Thecrude product was purified by preparative HPLC (method 6) to yield thedesired product (91.0 mg, 48%).

LC-MS (method 10): R_(t)=2.14 min; MS (ESIpos): m/z=469 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.63), 0.309(4.77), 0.320 (6.56), 0.331 (3.82), 0.345 (1.21), 0.441 (4.83), 0.460(5.07), 0.531 (0.65), 0.542 (1.57), 0.546 (1.70), 0.551 (0.81), 0.562(1.69), 0.566 (1.63), 0.577 (0.52), 0.997 (7.29), 1.016 (16.00), 1.035(7.63), 1.147 (0.46), 1.154 (0.42), 1.166 (0.68), 1.177 (0.57), 1.186(0.67), 1.196 (0.93), 1.207 (1.45), 1.214 (1.42), 1.226 (2.15), 1.238(1.39), 1.244 (1.39), 1.257 (0.71), 1.647 (2.30), 1.757 (1.24), 2.613(3.77), 2.672 (0.81), 2.713 (0.45), 3.829 (3.94), 3.845 (3.87), 4.068(4.03), 4.086 (3.97), 6.550 (0.41), 6.582 (0.43), 6.924 (0.40), 7.267(3.93), 7.289 (7.79), 7.311 (4.34), 7.342 (2.13), 7.358 (0.68), 7.370(1.98), 7.383 (3.15), 7.399 (2.25), 7.417 (0.64), 7.422 (0.59), 7.462(2.88), 7.466 (3.09), 7.479 (2.05), 7.490 (0.84), 7.501 (0.44), 7.630(0.52), 7.667 (1.06), 7.676 (1.44), 7.682 (1.66), 7.690 (3.16), 7.700(2.94), 7.713 (3.42), 7.728 (3.76), 7.736 (2.27), 7.742 (1.67), 7.751(1.08), 7.782 (1.81), 7.791 (1.46), 7.795 (1.64), 7.808 (1.23), 7.815(1.39), 7.822 (1.48), 7.854 (0.43), 7.890 (2.68), 7.902 (2.77), 8.472(6.57), 8.485 (6.26), 8.624 (0.74), 9.459 (0.68), 10.038 (7.04), 10.196(5.04).

Example 206N-[4-ethyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]-6-(3-methyl-1H-pyrazolo[3,4-c]pyridin-1-yl)pyrimidin-4-amine

A microwave vial was charged1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazolo [3,4-c]pyridine (100 mg,407 μmol), 4-ethyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-amine (98.2mg, 448 μmol) and sodium phenolate (61.4 mg, 529 μmol) and the contentswere suspended in 1,4-dioxane (2.5 ml, 29 mmol). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylidenaceton)dipalladium(4.85 mg, 5.29 μmol) and Xantphos (7.07 mg, 12.2 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously stirring. After coolingto ambient temperature, the reaction mixture was diluted with water andextracted with ethyl acetate (2×). The combined organic phases weredried Extrelut NT3 and concentrated under reduced pressure. The crudeproduct was purified by preparative HPLC (method 1) to yield the desiredproduct (85.4 mg, 49%).

LC-MS (method 10): R_(t)=1.91 min; MS (ESIpos): m/z=429 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.09), 0.008(0.89), 0.993 (6.14), 1.012 (13.66), 1.031 (6.52), 1.047 (0.45), 1.676(1.18), 1.758 (3.87), 2.064 (4.78), 2.476 (1.42), 2.620 (4.42), 2.631(5.03), 2.673 (0.51), 2.712 (2.33), 3.674 (16.00), 5.756 (2.22), 7.260(3.46), 7.282 (6.54), 7.304 (3.70), 7.315 (1.05), 7.355 (0.46), 7.506(0.47), 7.526 (0.57), 7.673 (2.11), 7.688 (2.92), 7.707 (2.04), 7.893(2.54), 7.906 (2.74), 8.474 (5.37), 8.487 (5.19), 8.521 (0.47), 8.535(0.46), 8.554 (0.42), 8.567 (0.42), 8.633 (0.97), 8.832 (0.49), 9.407(0.41), 10.039 (5.58), 10.106 (0.43).

Example 207N-[4-chloro-1-(cyclopropylmethyl)-5-(4-fluorophenyl)-1H-pyrazol-3-yl]-6-(3-methyl-1H-pyrazolo[3,4-c]pyridin-1-yl)pyrimidin-4-amine

A microwave vial was charged1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazolo[3,4-c]pyridine (75.0 mg,305 μmol),4-chloro-1-(cyclopropylmethyl)-5-(4-fluorophenyl)-1H-pyrazol-3-amine(89.2 mg, 336 μmol) and sodium phenolate (46.1 mg, 397 μmol) and thecontents were suspended in 1,4-dioxane (1.9 ml, 22 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (3.63 mg, 3.97 μmol) and Xantphos(5.30 mg, 9.16 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted water and extracted with ethyl acetate(2×). The combined organic phases were dried over Extrelut NT3 andconcentrated under reduced pressure. The crude product was purified bypreparative HPLC (method 8) to yield the desired product (14.2 mg, 9%).

LC-MS (method 9): R_(t)=1.17 min; MS (ESIpos): m/z=475 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.008 (1.98), 0.265(2.59), 0.278 (2.73), 0.490 (0.85), 0.501 (2.34), 0.504 (2.40), 0.520(2.50), 0.536 (0.70), 0.814 (0.43), 1.105 (0.63), 1.112 (0.62), 1.124(0.96), 1.136 (0.59), 1.143 (0.59), 1.234 (0.41), 1.648 (1.05), 2.328(0.42), 2.627 (16.00), 2.670 (0.52), 2.710 (0.44), 3.924 (4.52), 3.942(4.45), 5.754 (0.87), 7.366 (0.68), 7.382 (0.86), 7.394 (0.82), 7.419(2.26), 7.441 (4.94), 7.463 (2.97), 7.607 (3.03), 7.613 (1.86), 7.621(4.07), 7.629 (3.50), 7.637 (1.43), 7.643 (2.44), 7.897 (2.26), 7.911(2.41), 8.472 (3.30), 8.486 (3.19), 8.656 (3.51), 9.737 (3.72), 10.060(3.55).

Example 2084-(4-{[6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-3,5-dimethyl-1H-pyrazol-1-yl)benzonitrile

A microwave vial was charged4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (104 mg,428 μmol), 4-(4-amino-3,5-dimethyl-1H-pyrazol-1-yl)benzonitrile (100 mg,471 μmol) and sodium phenolate (54.7 mg, 471 μmol) and the contents weresuspended in 1,4-dioxane (3.1 ml, 36 mmol). The reaction mixture wasdegassed with Ar for 3 min. Tris(dibenzylidenaceton)dipalladium (5.10mg, 5.57 μmol) and Xantphos (7.43 mg, 12.8 μmol) were added and thereaction mixture was degassed again for 1 min. The vial was sealed andheated at 85° C. overnight while vigorously stirring. After cooling toambient temperature, the reaction mixture was purified by preparativeHPLC (method: column: Reprosil C18; 10 μm; 125×40 mm/flow: 75mL/min/solvent: A=water (0.1% formic acid), B=acetonitrile/gradient:0.00-5.50 min=10% B, 17.65-19.48 min=95% B, 19.66 min=10% B) to yieldthe desired product (102 mg, 54%).

LC-MS (method 9): R_(t)=1.12 min; MS (ESIpos): m/z=419 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.006 (1.09), 0.006(0.58), 2.074 (1.33), 2.104 (16.00), 2.211 (1.03), 2.292 (8.87), 2.633(13.19), 7.462 (0.41), 7.811 (1.50), 7.827 (1.47), 7.981 (2.77), 7.998(2.28), 9.039 (1.09).

Example 2094-(5-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-4-ethyl-1-methyl-1H-pyrazol-3-yl)benzonitrile

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (125 mg, 599 μmol),4-(5-amino-4-ethyl-1-methyl-1H-pyrazol-3-yl)benzonitrile (190 mg, 839μmol) and sodium phenolate (104 mg, 899 μmol) and the contents weresuspended in 1,4-dioxane (2.5 ml, 29 mmol). The reaction mixture wasdegassed with Ar for 3 min. Tris(dibenzylidenaceton)dipalladium (7.13mg, 7.79 μmol) and Xantphos (10.4 mg, 18.0 μmol) were added and thereaction mixture was degassed again for 1 min. The vial was sealed andheated at 85° C. overnight while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with water andextracted with ethyl acetate (2×). The combined organic phases weredried over Extrelut NT3 and concentrated under reduced pressure. Thecrude product was purified by preparative HPLC (method 1) to yield thedesired product (88.8 mg, 37%).

LC-MS (method 9): R_(t)=1.06 min; MS (ESIpos): m/z=399 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.71), 0.991(3.93), 1.010 (8.75), 1.028 (4.11), 2.178 (3.93), 2.524 (2.90), 2.561(0.97), 2.633 (16.00), 3.675 (13.09), 5.755 (0.70), 6.150 (3.36), 7.848(2.00), 7.869 (5.81), 7.890 (7.92), 7.911 (2.56), 8.469 (1.15), 9.415(1.88).

Example 2104-(3-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-4-ethyl-1-methyl-1H-pyrazol-5-yl)benzonitrile

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (95.0 mg, 455 μmol),4-(3-amino-4-ethyl-1-methyl-1H-pyrazol-5-yl)benzonitrile (124 mg, 546μmol) and sodium phenolate (79.3 mg, 683 μmol) and the contents weresuspended in 1,4-dioxane (1.9 ml, 22 mmol). The reaction mixture wasdegassed with Ar for 3 min. Tris(dibenzylidenaceton)dipalladium (5.42mg, 5.92 μmol) and Xantphos (7.90 mg, 13.7 μmol) were added and thereaction mixture was degassed again for 1 min. The vial was sealed andheated at 85° C. overnight while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with water andextracted with ethyl acetate (2×). The combined organic phases weredried over Extrelut NT3 and concentrated under reduced pressure. Thecrude product was purified by preparative HPLC (method 6) to yield thedesired product (30.1 mg, 15%).

LC-MS (method 9): R_(t)=1.03 min; MS (ESIpos): m/z=399 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.96), 0.008(0.82), 0.874 (3.47), 0.893 (7.92), 0.911 (3.58), 2.181 (14.36), 2.319(0.93), 2.337 (2.73), 2.356 (2.56), 2.367 (0.54), 2.375 (0.84), 2.524(0.45), 2.623 (12.99), 3.697 (16.00), 6.132 (3.44), 7.338 (2.77), 7.689(4.16), 7.710 (4.86), 8.007 (4.61), 8.027 (4.13), 8.445 (2.99), 9.371(2.84).

Example 2114-(1,4-dimethyl-5-{[6-(3-methyl-4-oxo-5,6-dihydrocyclopenta[c]pyrazol-1(4H)-yl)pyrimidin-4-yl]amino}-1H-pyrazol-3-yl)benzonitrile

A microwave vial was charged with4-(5-amino-1,4-dimethyl-1H-pyrazol-3-yl)benzonitrile (93.9 mg, 442μmol),1-(6-chloropyrimidin-4-yl)-3-methyl-5,6-dihydrocyclopenta[c]pyrazol-4(1H)-one(100 mg, 402 μmol) and sodium phenolate (51.4 mg, 442 μmol) and thecontents were suspended in 1,4-dioxane (1.2 mL). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium(5.52 mg, 6.03 μmol) and XantPhos (6.98 mg, 12.1 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously shaking. After coolingto ambient temperature, the reaction mixture was filtered andconcentrated. The residue was redissolved in dimethylsulfoxide andpurified by preparative HPLC (X-Bridge C18 5 μm 100×30 mm, solvent A:water, solvent B: acetonitrile, flow: 65 mL/min plus 5 mL/min 2% NH3 inwater, gradient: 0-2 min 10% solvent B, 2-2.2 min to 30% solvent B,2.2-7 min to 70% solvent B, 7-7.5 min to 92% solvent B, 7.5-9 min at 92%B) to yield the desired product (17.5 mg, 9% yield).

LC-MS (method 10): R_(t)=1.71 min; MS (ESIpos): m/z=425 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (2.37), 0.008(2.19), 2.079 (16.00), 2.308 (1.90), 2.365 (1.30), 2.670 (0.43), 2.861(0.45), 2.941 (1.71), 2.947 (1.71), 2.953 (1.96), 2.960 (1.79), 2.966(1.84), 3.340 (2.11), 3.347 (1.93), 3.353 (2.06), 3.358 (1.85), 3.365(1.79), 3.704 (6.45), 7.902 (11.30), 8.531 (0.42).

Example 2124-[1-(2-cyclopropylethyl)-3-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-4-methyl-1H-pyrazol-5-yl]benzonitrile

A microwave vial was charged with4-[3-amino-1-(2-cyclopropylethyl)-4-methyl-1H-pyrazol-5-yl]benzonitrile(50.0 mg, 188 μmol), 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine(43.1 mg, 206 μmol) and sodium phenolate (24.0 mg, 206 μmol) and thecontents were suspended in 1,4-dioxane (0.6 mL). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium(3.26 mg, 5.63 μmol) and XantPhos (2.58 mg, 2.82 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously stirring. After coolingto ambient temperature, the reaction mixture was filtered andconcentrated. The residue was redissolved in dimethylsulfoxide andpurified by preparative HPLC (method 6) to yield the desired product(17.5 mg, 21% yield).

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.60), −0.135(0.83), −0.124 (3.18), −0.112 (3.34), −0.098 (0.89), −0.008 (5.08),0.008 (3.84), 0.146 (0.50), 0.275 (0.85), 0.289 (2.57), 0.295 (1.41),0.305 (2.86), 0.309 (2.72), 0.319 (0.89), 0.472 (0.68), 0.491 (0.89),1.564 (1.06), 1.581 (3.05), 1.598 (3.03), 1.615 (1.06), 1.878 (14.15),2.168 (16.00), 2.328 (0.73), 2.366 (0.75), 2.624 (14.71), 2.670 (0.77),2.710 (0.79), 4.023 (2.03), 4.039 (4.09), 4.057 (1.97), 6.126 (4.13),7.562 (0.83), 7.662 (4.88), 7.684 (5.52), 8.003 (5.42), 8.024 (4.75),8.461 (3.74), 9.475 (3.44).

Example 213 ethyl1-(6-{[3-(4-cyanophenyl)-1,4-dimethyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

A microwave vial was charged ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (250mg, 891 μmol), 4-(5-amino-1,4-dimethyl-1H-pyrazol-3-yl)benzonitrile (208mg, 980 μmol) and sodium phenolate (155 mg, 1.34 mmol) and the contentswere suspended in 1,4-dioxane (4.0 ml, 46 mmol). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylidenaceton)dipalladium(10.6 mg, 11.6 μmol) and Xantphos (15.5 mg, 26.7 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously stirring. After coolingto ambient temperature, the reaction mixture was diluted with saturatedsodium bicarbonate solution and extracted with ethyl acetate (2×). Thecombined organic phases were washed with brine, dried over sodiumsulfate and concentrated under reduced pressure. The crude product wastriturated with diethyl ether, the precipitate was collected byfiltration, dreid and purified by preparative HPLC (method: column:Reprosil C18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent: A=water (0.1%formic acid), B=acetonitrile/gradient: 0.00-4.25 min=20% B, 4.50 min=30%B, 19.00-22.50 min=100% B, 22.75-25.00min=20%) to yield the desiredproduct (141 mg, 35%).

LC-MS (method 10): R_(t)=2.07 min; MS (ESIpos): m/z=457 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.290 (3.11), 1.307(6.43), 1.325 (3.17), 2.076 (14.85), 2.379 (2.45), 2.911 (11.63), 3.702(8.12), 4.230 (0.92), 4.248 (2.80), 4.266 (2.77), 4.284 (0.90), 7.896(16.00), 8.546 (0.48), 9.635 (0.96).

Example 2144-(4-methoxy-3-{[6-(3-methyl-1H-pyrazolo[3,4-c]pyridin-1-yl)pyrimidin-4-yl]amino}-1H-pyrazol-5-yl)benzonitrile

A microwave vial was charged1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazolo[3,4-c]pyridine (104 mg,424 μmol), 4-(3-amino-4-methoxy-1H-pyrazol-5-yl)benzonitrile (100 mg,467 μmol) and sodium phenolate (54.2 mg, 467 μmol) and the contents weresuspended in 1,4-dioxane (3.0 ml, 35 mmol). The reaction mixture wasdegassed with Ar for 3 min. Tris(dibenzylidenaceton)dipalladium (5.05mg, 5.52 μmol) and Xantphos (7.37 mg, 12.7 μmol) were added and thereaction mixture was degassed again for 1 min. The vial was sealed andheated at 85° C. overnight while vigorously stirring. After cooling toambient temperature, the reaction mixture was purified by preparativeHPLC (method: column: Reprosil C18; 10 μm; 125×40 mm/flow: 75mL/min/solvent: A=water (0.1% formic acid), B=acetonitrile/gradient:0.00-5.50 min=10% B, 17.65-19.48 min=95% B, 19.66 min=10% B) andsubsequently by flash-chromatography (column: Biotage KP-Sil 10 g;solvent A: dichloromethane 98% , solvent B: methanol 2%) to yield thedesired product (3.7 mg, 2%).

LC-MS (method 10): R_(t)=2.16 min; MS (ESIpos): m/z=424 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (1.05), −0.008(14.55), 0.008 (9.18), 0.146 (1.05), 1.235 (0.41), 1.780 (1.05), 2.031(0.86), 2.214 (1.95), 2.227 (0.95), 2.328 (1.00), 2.366 (1.00), 2.524(4.36), 2.670 (1.27), 2.686 (2.23), 2.711 (15.05), 3.162 (0.64), 3.175(0.59), 3.729 (16.00), 6.975 (3.91), 7.673 (0.59), 7.971 (5.55), 7.983(2.64), 7.986 (2.73), 7.993 (4.73), 8.158 (4.73), 8.179 (3.55), 8.268(3.73), 8.552 (2.86), 8.565 (2.64), 8.837 (0.55), 9.063 (3.82), 9.065(3.45), 10.095 (3.00).

Example 2151-[1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]cyclobutanol

Under an argon atmosphere,6-(4-bromo-3,5-dimethyl-1H-pyrazol-1-yl)-N-[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]pyrimidin-4-amine(24.2 mg, 51.5 μmol) was dissolved in tetrahydrofuran (0.5 mL) andcooled to −15° C. A solution of i-PrMgCl*LiCl (99 μl, 1.3 M, 130 μmol)was added slowly and stirred for 20 min at −15° C. and 50 min at 0° C.cyclobutanone (7.7 μl, 100 μmol) was then added at 0° C. and thereaction mixture was strirred for 15 min. A second aliquot ofcyclobutanone (7.7 μl, 100 μmol) was added and the reaction mixturestirred for further 40 min. It was then quenched by careful addition ofsat. aqueous ammonium chloride solution, diluted with water andextracted with ethyl acetate. The organic phase extract was washed withbrine, dried over sodium sulfate and concentrated. The residue waspurified by flash column chromatography (KP Sil 10 g, cyclohexane/ethylacetate gradient 88/12 to 0/100) to yield the desired product (4.0 mg,17% yield).

LC-MS (method 10): R_(t)=2.01 min; MS (ESIpos): m/z=462 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (1.37), 0.006(0.92), 0.872 (3.36), 0.887 (7.33), 0.902 (3.32), 1.161 (2.11), 1.175(4.27), 1.189 (2.15), 1.734 (0.54), 1.744 (0.45), 1.754 (0.67), 1.988(8.05), 2.118 (0.79), 2.163 (0.87), 2.181 (13.77), 2.201 (0.53), 2.215(0.53), 2.228 (1.09), 2.234 (0.79), 2.245 (1.34), 2.252 (1.12), 2.261(1.01), 2.286 (0.78), 2.301 (2.22), 2.316 (2.13), 2.327 (1.08), 2.519(1.70), 2.523 (1.48), 2.579 (14.13), 2.613 (0.53), 2.706 (0.79), 3.643(16.00), 4.008 (0.62), 4.023 (1.85), 4.037 (1.84), 4.051 (0.60), 5.149(5.43), 5.754 (1.53), 7.304 (1.66), 7.360 (2.06), 7.364 (0.79), 7.378(4.43), 7.391 (0.87), 7.395 (2.53), 7.499 (2.49), 7.504 (1.14), 7.510(2.76), 7.517 (2.26), 7.523 (0.92), 7.528 (1.93), 8.440 (2.94), 9.324(1.76).

Example 2164-[5-({6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-yl}amino)-4-ethyl-1-methyl-1H-pyrazol-3-yl]benzonitrile

A microwave vial was charged4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (125mg, 511 μmol), 4-(5-amino-4-ethyl-1-methyl-1H-pyrazol-3-yl)benzonitrile(162 mg, 715 μmol) and sodium phenolate (89.0 mg, 766 μmol) and thecontents were suspended in 1,4-dioxane (2.1 ml, 25 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (6.08 mg, 6.64 μmol) and Xantphos(8.87 mg, 15.3 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with water and extracted with ethyl acetate(2×). The combined organic phases were dried over Extrelut NT3 andconcentrated under reduced pressure. The crude product was purified bypreparative HPLC (method 6) to yield the desired product (89.0 mg, 38%).

LC-MS (method 10): R_(t)=2.13 min; MS (ESIpos): m/z=435 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.990 (6.46), 1.009(13.80), 1.027 (6.69), 1.567 (0.92), 2.087 (0.41), 2.292 (4.45), 2.368(0.40), 2.563 (1.57), 2.705 (0.61), 3.682 (16.00), 6.791 (4.58), 7.684(2.18), 7.820 (4.47), 7.851 (3.15), 7.871 (7.37), 7.892 (10.37), 7.912(3.55), 7.956 (1.94), 8.499 (1.17), 9.597 (1.60).

Example 2174-[3-({6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-yl}amino)-4-ethyl-1-methyl-1H-pyrazol-5-yl]benzonitrile

A microwave vial was charged4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (110mg, 450 μmol), 4-(3-amino-4-ethyl-1-methyl-1H-pyrazol-5-yl)benzonitrile(122 mg, 540 μmol) and sodium phenolate (78.3 mg, 674 μmol) and thecontents were suspended in 1,4-dioxane (1.9 ml, 22 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (5.35 mg, 5.85 μmol) and Xantphos(7.81 mg, 13.5 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with water and extracted with ethyl acetate(2×). The combined organic phases were dried over Extrelut NT3 andconcentrated under reduced pressure. The crude product was purified bypreparative HPLC (method 6) and subsequently by flash-chromatography(column: Biotage KP-Sil 10 g; dichloromethane/ethyl acetate) to yieldthe desired product (58.4 mg, 28%).

LC-MS (method 10): R_(t)=2.13 min; MS (ESIpos): m/z=435 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (2.53), 0.008(2.42), 0.874 (3.44), 0.893 (7.91), 0.911 (3.56), 1.566 (0.79), 2.293(13.66), 2.324 (0.92), 2.342 (2.31), 2.361 (2.24), 2.380 (0.76), 3.695(0.80), 3.708 (16.00), 6.772 (4.01), 7.392 (1.61), 7.695 (4.64), 7.716(4.99), 7.827 (2.48), 7.963 (1.06), 8.010 (4.98), 8.031 (4.32), 8.477(3.05), 9.585 (1.73).

Example 218N-[4-chloro-1-(cyclopropylmethyl)-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-6-(3-methyl-1H-pyrazolo[3,4-c]pyridin-1-yl)pyrimidin-4-amine

A microwave vial was charged1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazolo[3,4-c]pyridine (75.0 mg,305 μmol),4-chloro-1-(cyclopropylmethyl)-3-(4-fluorophenyl)-1H-pyrazol-5-amine(89.2 mg, 336 μmol) and sodium phenolate (46.1 mg, 397 μmol) and thecontents were suspended in 1,4-dioxane (1.9 ml, 22 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (3.63 mg, 3.97 μmol) and Xantphos(5.30 mg, 9.16 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with water and extracted with ethyl acetate(2×). The combined organic phases were dried over Extrelut NT3 andconcentrated under reduced pressure. The crude product was purified bypreparative HPLC (method 6) and subsequently by flash-chromatography onsilics gel (SNAP KP-Sil 10 g, dichloromethane/ethyl acetate) to yieldthe desired product (22.3 mg, 15%).

LC-MS (method 10): R_(t)=2.19 min; MS (ESIpos): m/z=475 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.008 (1.34), 0.328(1.73), 0.339 (6.54), 0.352 (6.92), 0.364 (1.93), 0.456 (2.04), 0.467(5.77), 0.486 (5.91), 0.501 (1.21), 1.232 (2.13), 1.240 (1.75), 1.252(2.31), 1.263 (1.45), 1.270 (1.48), 1.282 (0.89), 1.300 (0.44), 2.629(16.00), 2.671 (0.59), 3.927 (6.78), 3.944 (6.46), 7.320 (4.71), 7.342(8.97), 7.365 (4.54), 7.902 (4.79), 7.919 (7.54), 7.933 (5.29), 7.940(4.72), 7.954 (3.69), 8.483 (6.13), 8.497 (5.72), 8.654 (3.33), 9.762(3.04), 10.037 (7.37).

Example 219 ethyl1-(6-{[1-(4-cyanophenyl)-3,5-dimethyl-1H-pyrazol-4-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

A microwave vial was charged ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (120mg, 428 μmol), 4-(4-amino-3,5-dimethyl-1H-pyrazol-1-yl)benzonitrile (100mg, 471 μmol) and sodium phenolate (54.7 mg, 471 μmol) and the contentswere suspended in 1,4-dioxane (3.1 ml, 36 mmol). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylidenaceton)dipalladium(5.10 mg, 5.57 μmol) and Xantphos (7.43 mg, 12.8 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously stirring. After coolingto ambient temperature, the reaction mixture was diluted with saturatedsodium bicarbonate solution and extracted with ethyl acetate (2×). Thecombined organic phases were dried over sodium sulfate and concentratedunder reduced pressure. The remaining residue was taken up indichloromethane, an precipitate occurred which was collected byfiltration and dried to yield the desired product (80.0 mg, 39%).

LC-MS (method 10): R_(t)=2.02 min; MS (ESIpos): m/z=457 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.16), 1.287(2.63), 1.304 (5.18), 1.322 (2.69), 2.075 (0.68), 2.111 (16.00), 2.284(2.58), 2.293 (13.09), 2.369 (1.46), 2.387 (1.54), 2.888 (7.26), 4.226(0.83), 4.243 (2.30), 4.261 (2.32), 4.278 (0.86), 7.686 (0.44), 7.807(1.92), 7.828 (2.42), 7.858 (0.53), 7.979 (3.80), 8.001 (3.12), 9.120(0.95).

Example 2203-[1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]oxetan-3-ol

Under an argon atmosphere,6-(4-bromo-3,5-dimethyl-1H-pyrazol-1-yl)-N-[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]pyrimidin-4-amine(45.0 mg, 95.7 μmol) was dissolved in tetrahydrofuran (0.95 mL) andcooled to −15° C. A solution of i-PrMgCl*LiCl (180 μl, 1.3 M, 240 μmol)was added slowly and stirred for 50 min at −15° C. , when a secondaliquot of i-PrMgCl*LiCl (180 μl, 1.3 M, 240 μmol) was added. After 50min stirring at −15° C., (180 μl, 1.3 M, 240 μmol) was added at ambienttemperature. The reaction mixture was strirred for 50 min. It was thenquenched by careful addition of sat. aqueous ammonium chloride solution,diluted with water and extracted with ethyl acetate. The organic phaseextract was washed with brine, dried over sodium sulfate andconcentrated. The residue was purified by flash column chromatography(KP Sil 25 g, dichloromethane/methanol 98/2 to 90/10) to yield thedesired product (5.0 mg, 10% yield).

LC-MS (method 10): R_(t)=1.67 min; MS (ESIpos): m/z=464 [M+H]⁺

¹H-NMR (600 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.692 (0.69), 0.703(0.67), 0.729 (0.72), 0.740 (0.75), 0.811 (0.81), 0.822 (1.32), 0.832(0.88), 0.842 (0.47), 0.854 (0.55), 0.876 (2.99), 0.888 (6.00), 0.901(2.90), 1.237 (1.92), 1.424 (2.88), 1.543 (2.02), 2.065 (0.72), 2.108(10.81), 2.161 (1.05), 2.292 (0.85), 2.305 (2.20), 2.317 (2.12), 2.330(0.76), 2.485 (12.62), 2.612 (0.42), 2.910 (0.57), 3.568 (0.53), 3.643(11.86), 4.411 (0.47), 4.421 (0.42), 4.542 (0.57), 4.658 (3.47), 4.669(3.69), 5.012 (3.52), 5.023 (3.30), 5.396 (0.44), 5.747 (16.00), 5.953(0.50), 5.995 (4.14), 7.329 (1.60), 7.361 (1.53), 7.375 (3.29), 7.390(1.91), 7.499 (1.88), 7.508 (2.38), 7.522 (1.66), 7.901 (0.43), 8.455(2.80), 9.350 (1.74).

Example 2214-[5-{[6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-1-(2-cyclopropylethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile

A microwave vial was charged with4-[5-amino-1-(2-cyclopropylethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(50.0 mg, 188 μmol),4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (50.2 mg,206 μmol) and sodium phenolate (24.0 mg, 206 μmol) and the contents weresuspended in 1,4-dioxane (0.58 mL). The reaction mixture was degassedwith Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (2.58 mg, 2.82μmol) and XantPhos (3.26 mg, 5.63 μmol) were added and the reactionmixture was degassed again for 1 min. The vial was sealed and heated at85° C. overnight while vigorously shaking. After cooling to ambienttemperature, the reaction mixture was filtered and concentrated. Theresidue was redissolved in dimethylsulfoxide and purified by preparativeHPLC (method 8) to yield the desired product (32 mg, 36% yield).

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.82), −0.063(3.04), −0.054 (3.08), −0.008 (7.01), 0.008 (6.29), 0.146 (0.80), 0.306(1.94), 0.323 (2.08), 0.622 (0.78), 1.356 (0.72), 1.629 (0.96), 1.647(2.70), 1.665 (2.64), 1.682 (0.94), 2.058 (15.72), 2.073 (1.14), 2.208(2.14), 2.328 (0.66), 2.366 (0.64), 2.648 (16.00), 2.670 (0.82), 2.710(0.62), 4.036 (1.94), 7.897 (12.34), 7.921 (0.66), 8.498 (0.50), 9.515(0.50).

Example 2224-[3-{[6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-1-(2-cyclopropylethyl)-4-methyl-1H-pyrazol-5-yl]benzonitrile

A microwave vial was charged with4-[3-amino-1-(2-cyclopropylethyl)-4-methyl-1H-pyrazol-5-yl]benzonitrile(44.0 mg, 165 μmol),4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (44.2 mg,182 μmol) and sodium phenolate (21.1 mg, 182 μmol) and the contents weresuspended in 1,4-dioxane (0.5 mL). The reaction mixture was degassedwith Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (2.27 mg, 2.48μmol) and XantPhos (2.87 mg, 4.96 μmol) were added and the reactionmixture was degassed again for 1 min. The vial was sealed and heated at85° C. overnight while vigorously shaking. After cooling to ambienttemperature, the reaction mixture was filtered and concentrated. Theresidue was redissolved in dimethylsulfoxide and purified by preparativeHPLC (method 8) to yield the desired product (25 mg, 33% yield).

LC-MS (method 11): R_(t)=1.67 min; MS (ESIpos): m/z=473 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.47), −0.137(0.67), −0.126 (2.56), −0.114 (2.70), −0.101 (0.78), −0.054 (0.41),−0.008 (3.63), 0.008 (3.13), 0.146 (0.41), 0.274 (0.73), 0.284 (1.96),0.288 (2.12), 0.294 (1.24), 0.304 (2.55), 0.308 (2.37), 0.318 (0.93),0.470 (0.54), 0.489 (0.75), 1.356 (0.89), 1.562 (0.83), 1.579 (2.43),1.596 (2.42), 1.613 (0.84), 1.881 (10.37), 2.059 (1.74), 2.073 (0.95),2.205 (13.73), 2.367 (0.46), 2.524 (0.97), 2.644 (16.00), 2.670 (0.52),2.711 (0.47), 4.023 (1.73), 4.040 (3.51), 4.057 (1.72), 7.662 (4.00),7.683 (4.65), 7.897 (1.35), 8.004 (4.50), 8.025 (4.09), 8.498 (2.89),9.603 (2.32).

Example 223N-[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3-methyl-1H-pyrazolo[4,3-b]pyridin-1-yl)pyrimidin-4-amine

A microwave vial was charged with4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (100 mg, 456μmol), 1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazolo [4,3-b]pyridine(123 mg, 502 μmol) and sodium phenolate (63.5 mg, 547 μmol) and thecontents were suspended in 1,4-dioxane (1.3 mL). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium(6.26 mg, 6.84 μmol) and XantPhos (7.92 mg, 13.7 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 90° C. overnight while vigorously shaking. After coolingto ambient temperature, the reaction mixture was filtered andconcentrated. The residue was redissolved in dimethylsulfoxide andpurified by preparative HPLC (method 3) to yield the desired product(105 mg, 51% yield).

LC-MS (method 9): Rt=1.12 min; MS (ESIpos): m/z=429 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (1.19), 0.007(0.79), 0.892 (3.29), 0.908 (7.42), 0.922 (3.26), 2.321 (0.71), 2.336(2.01), 2.351 (1.95), 2.366 (0.72), 2.633 (16.00), 3.688 (13.85), 7.374(2.05), 7.378 (1.07), 7.388 (1.01), 7.392 (4.22), 7.397 (0.90), 7.406(0.81), 7.410 (2.41), 7.463 (0.53), 7.466 (0.53), 7.478 (0.41), 7.496(1.05), 7.524 (2.46), 7.529 (1.03), 7.535 (2.55), 7.542 (2.08), 7.549(0.83), 7.553 (1.79), 7.579 (1.86), 7.588 (1.79), 7.596 (1.75), 7.605(1.79), 8.560 (2.81), 8.657 (2.04), 8.660 (2.06), 8.666 (1.99), 8.669(1.85), 9.015 (1.97), 9.018 (1.97), 9.033 (1.89), 9.035 (1.73), 9.435(1.86).

Example 224N-[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3-methyl-1H-pyrazolo[4,3-c]pyridin-1-yl)pyrimidin-4-amine

A microwave vial was charged with1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazolo[4,3-c]pyridine (123 mg,502 μmol) and sodium phenolate (63.5 mg, 547 μmol) and the contents weresuspended in 1,4-dioxane (1.3 mL). The reaction mixture was degassedwith Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (7.92 mg, 13.7μmol), XantPhos (6.26 mg, 6.84 μmol) and4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (100 mg, 456μmol) were added and the reaction mixture was degassed again for 1 min.The reaction mixture was stirred at 90° C. bath temperature overnight.After cooling to ambient temperature, the reaction mixture was filteredand concentrated. The residue was redissolved in dimethylsulfoxide andpurified by preparative HPLC (method 7) to yield the desired product (5mg, 2% yield).

LC-MS (method 10): R_(t)=1.63 min; MS (ESIpos): m/z=429 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.120 (0.44), −0.007(4.92), 0.006 (3.32), 0.117 (0.44), 0.887 (3.48), 0.902 (7.95), 0.917(3.58), 0.995 (0.65), 2.316 (0.74), 2.331 (2.09), 2.346 (2.06), 2.362(1.36), 2.519 (1.32), 2.523 (0.94), 2.636 (0.86), 2.670 (16.00), 2.675(3.47), 2.711 (0.68), 3.401 (1.00), 3.682 (14.85), 7.285 (0.67), 7.293(0.47), 7.308 (0.47), 7.372 (2.29), 7.390 (4.58), 7.408 (2.58), 7.494(1.06), 7.505 (0.79), 7.520 (2.85), 7.531 (2.85), 7.538 (2.36), 7.544(0.98), 7.549 (1.98), 8.556 (1.06), 8.568 (4.18), 8.570 (4.27), 8.574(6.62), 8.578 (3.12), 8.586 (1.47), 8.636 (0.48), 8.648 (0.48), 8.814(0.58), 9.191 (4.15), 9.193 (4.05), 9.231 (0.53), 9.469 (1.64).

Example 225N-[1-(cyclopropylmethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]-6-[3,5-dimethyl-4-(5-methyl-1,3,4-oxadiazol-2-yl)-1H-pyrazol-1-yl]pyrimidin-4-amine

A solution ofN′-acetyl-1-(6-{[1-(cyclopropylmethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbohydrazide(95.4 mg, 179 μmol) in tetrahydrofuran (2.5 ml, 31 mmol) was treatedwith Burgess reagent (59.9 mg, 251 μmol) and stirred overnight atambient temperature. The micture was purified by preparative HPLC(method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent:A=water (0.01% formic acid), B=acetonitrile/gradient: 0.00-5.00 min=10%B, 6.50 min=20% B, 17.0-19.75 min=100% B, 19.75-23.00 min=90% B) toyield the desired product (49.1 mg, 53%).

LC-MS (method 10): R_(t)=2.15 min; MS (ESIpos): m/z=514 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.304 (3.03), 0.314(3.14), 0.442 (3.39), 0.462 (3.52), 0.983 (4.25), 1.002 (8.98), 1.020(4.39), 1.181 (0.53), 1.193 (0.96), 1.200 (0.95), 1.212 (1.37), 1.231(1.03), 1.426 (1.76), 2.369 (0.43), 2.469 (4.21), 2.571 (16.00), 2.973(15.38), 3.808 (2.47), 3.822 (2.48), 3.991 (0.85), 7.258 (2.62), 7.280(5.38), 7.302 (3.05), 7.692 (2.55), 8.543 (0.55), 9.489 (0.41).

Example 2266-[3,5-dimethyl-4-(5-methyl-1,3,4-oxadiazol-2-yl)-1H-pyrazol-1-yl]-N-[4-ethyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]pyrimidin-4-amine

A solution ofN′-acetyl-1-(6-{[4-ethyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbohydrazide(65.1 mg, 132 μmol) in tetrahydrofuran (2.5 ml, 31 mmol) was treatedwith Burgess reagent (44.2 mg, 185 μmol) and stirred overnight atambient temperature. The micture was purified by preparative HPLC(method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent:A=water (0.01% formic acid), B=acetonitrile/gradient: 0.00-5.00 min=10%B, 6.50 min=20% B, 17.0-19.75 min=100% B, 19.75-23.00 min=90% B) toyield the desired product (20.0 mg, 29%).

LC-MS (method 10): R_(t)=1.94 min; MS (ESIpos): m/z=474 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.52), 0.146(0.42), 0.978 (4.01), 0.997 (8.45), 1.015 (4.11), 1.234 (0.60), 1.760(0.46), 1.904 (0.83), 2.328 (0.98), 2.366 (0.81), 2.473 (5.09), 2.573(16.00), 2.670 (1.02), 2.710 (0.79), 2.773 (1.00), 2.976 (15.46), 3.602(0.50), 3.652 (10.06), 7.251 (2.32), 7.273 (4.78), 7.295 (2.73), 7.654(1.81), 7.668 (2.50), 7.687 (1.79), 8.560 (0.75), 9.544 (0.94).

Example 2274-[5-({6-[(±)-4-hydroxy-3,4-dimethyl-5,6-dihydrocyclopenta[c]pyrazol-1(4H)-yl]pyrimidin-4-yl}amino)-1,4-dimethyl-1H-pyrazol-3-yl]benzonitrile(racemate)

4-(1,4-dimethyl-5-{[6-(3-methyl-4-oxo-5,6-dihydrocyclopenta[c]pyrazol-1(4H)-yl)pyrimidin-4-yl]amino}-1H-pyrazol-3-yl)benzonitrile(15.5 mg, 36.5 μmol) was dissolved in tetrahydrofuran (0.5 mL) andchilled with a water bath. A solution of methylmagnesium bromide (1501.0 M, 150 μmol) was added. After 30 min stirring, a second aliquot ofmethylmagnesium bromide (80 μL, 1.0 M, 80 μmol) was added and thereaction mixture stirred for another 20 min. It was then quenched bycareful addition of sat. aqueous ammonium chloride solution andextracted with ethyl acetate (3×). The combined organic phase extractswere dried over sodium sulfate and concentrated. The residue waspurified by flash column chromatography (SNAP Ultra 10 g,dichloromethane/methanol gradient 98/2 to 96/4) to yield the desiredproduct (4.8 mg, 27% yield).

LC-MS (method 10): R_(t)=1.66 min; MS (ESIpos): m/z=441 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.120 (0.45), −0.007(5.87), 0.007 (2.99), 1.235 (1.85), 1.451 (7.02), 1.478 (1.26), 2.067(16.00), 2.079 (1.69), 2.201 (2.52), 2.362 (0.72), 2.438 (1.22), 2.448(1.26), 2.456 (1.41), 2.465 (2.24), 2.606 (0.82), 2.635 (0.73), 2.976(0.56), 2.997 (1.78), 3.010 (0.72), 3.020 (0.52), 3.103 (0.68), 3.120(0.80), 3.129 (0.82), 3.147 (0.65), 3.568 (0.42), 3.690 (8.44), 4.966(3.34), 5.754 (2.18), 7.899 (12.87), 8.432 (0.72), 9.453 (1.03).

Example 228 4-(1,4-dimethyl-3-{[6-(3-methyl-1H-pyrazolo[3,4-c]pyridin-1-yl)pyrimidin-4-yl]amino}-1H-pyrazol-5-yl)benzonitrile

Under an argon atmosphere,1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazolo[3,4-c]pyridine (82.8 mg,337 μmol) and sodium phenolate (53.3 mg, 459 μmol) were suspended in1,4-dioxane (0.88 mL). The reaction mixture was degassed with Ar for 3min. Tris(dibenzylideneacetone)dipalladium (4.21 mg, 4.59 μmol),XantPhos (5.32 mg, 9.19 μmol) and4-(3-amino-1,4-dimethyl-1H-pyrazol-5-yl)benzonitrile (65.0 mg, 306 μmol)were added and the reaction mixture was degassed again for 1 min. Thevial was sealed and heated at 90° C. overnight while vigorously shaking.After cooling to ambient temperature, the reaction mixture was dilutedwith dichloromethane and concentrated. It was redissolved indimethylsulfoxide, filtered and purified by preparative HPLC (method 7)to yield the desired product (41 mg, 32% yield).

LC-MS (method 10): R_(t)=1.67 min; MS (ESIpos): m/z=422 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.10), 0.008(1.07), 1.920 (13.57), 2.636 (15.68), 3.771 (16.00), 5.755 (2.88), 7.551(1.05), 7.719 (4.31), 7.740 (4.98), 7.892 (1.98), 7.895 (2.07), 7.905(2.08), 7.908 (2.15), 8.016 (5.06), 8.037 (4.34), 8.465 (3.26), 8.479(3.09), 8.618 (3.47), 9.567 (2.80), 10.063 (3.51).

Example 229N-[4-ethyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]-6-(3-methyl-1H-pyrazolo[4,3-b]pyridin-1-yl)pyrimidin-4-amine

Under an argon atmosphere,1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazolo[4,3-b]pyridine (123 mg,502 μmol) and sodium phenolate (79.4 mg, 684 μmol) were suspended in1,4-dioxane (1.3 mL). The reaction mixture was degassed with Ar for 3min. Tris(dibenzylideneacetone)dipalladium (6.26 mg, 6.84 XantPhos (7.92mg, 13.7 μmol) and4-ethyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-amine (100 mg, 456μmol) were added and the reaction mixture was degassed again for 1 min.The vial was sealed and heated at 90° C. overnight while vigorouslyshaking. After cooling to ambient temperature, the reaction mixture wasdiluted with dichloromethane and concentrated. It was redissolved indimethylsulfoxide, filtered and purified by preparative HPLC (method 3)to yield the desired product (141 mg, 72% yield).

LC-MS (method 10): R_(t)=2.08 min; MS (ESIpos): m/z=429 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.39), 0.008(1.05), 0.993 (6.42), 1.012 (13.68), 1.031 (6.35), 1.567 (0.61), 2.476(2.56), 2.622 (5.06), 2.631 (6.29), 2.673 (0.52), 3.672 (16.00), 5.756(5.27), 7.260 (3.52), 7.269 (1.80), 7.271 (1.81), 7.282 (6.78), 7.295(1.54), 7.304 (3.73), 7.313 (1.26), 7.342 (0.45), 7.354 (0.54), 7.370(0.54), 7.383 (0.54), 7.400 (0.41), 7.462 (0.52), 7.466 (0.53), 7.506(0.60), 7.526 (0.69), 7.545 (0.48), 7.584 (4.03), 7.595 (4.06), 7.605(3.96), 7.616 (4.06), 7.628 (0.54), 7.639 (0.56), 7.649 (0.69), 7.660(1.14), 7.673 (2.43), 7.688 (3.13), 8.587 (1.18), 8.664 (3.82), 8.667(3.89), 8.675 (3.72), 8.678 (3.46), 8.785 (0.56), 8.787 (0.54), 8.993(4.20), 8.997 (4.12), 9.014 (4.07), 9.018 (3.70), 9.467 (2.33).

Example 230

N-[4-ethyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]-6-(3-methyl-1H-pyrazolo[4,3-c]pyridin-1-yl)pyrimidin-4-amine

Under an argon atmosphere,1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazolo[4,3-c]pyridine (123 mg,502 μmol) and sodium phenolate (79.4 mg, 684 μmol) were suspended in1,4-dioxane (1.3 mL). The reaction mixture was degassed with Ar for 3min. Tris(dibenzylideneacetone)dipalladium (6.26 mg, 6.84 μmol),XantPhos (7.92 mg, 13.7 μmol) and4-ethyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-amine (100 mg, 456μmol) were added and the reaction mixture was degassed again for 1 min.The vial was sealed and heated at 90° C. overnight while vigorouslyshaking. After cooling to ambient temperature, the reaction mixture wasdiluted with dichloromethane and concentrated. It was redissolved indimethylsulfoxide, filtered and purified by preparative HPLC (method 7)to yield the desired product (31 mg, 16% yield).

LC-MS (method 10): R_(t)=1.61 min; MS (ESIpos): m/z=429 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (1.19), −0.008(9.97), 0.008 (10.01), 0.146 (1.15), 0.986 (6.24), 1.004 (13.91), 1.023(6.52), 2.328 (1.85), 2.366 (1.48), 2.664 (6.56), 2.675 (9.07), 2.710(1.93), 3.664 (16.00), 5.754 (6.93), 7.257 (3.41), 7.280 (6.77), 7.302(3.86), 7.351 (0.70), 7.502 (0.86), 7.522 (1.15), 7.541 (0.62), 7.683(3.20), 8.542 (2.87), 8.557 (6.03), 8.583 (9.48), 8.598 (5.33), 8.636(1.39), 8.650 (1.03), 8.815 (1.07), 9.198 (4.72), 9.231 (1.15), 9.493(1.72).

Example 2314-[1-(cyclopropylmethyl)-4-methyl-5-{[6-(3-methyl-1H-pyrazolo[3,4-c]pyridin-1-yl)pyrimidin-4-yl]amino}-1H-pyrazol-3-yl]benzonitrile

Under an argon atmosphere,1(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazolo[3,4-c]pyridine (161 mg,654 μmol) and sodium phenolate (104 mg, 892 μmol) were suspended in1,4-dioxane (1.7 mL). The reaction mixture was degassed with Ar for 3min. Tris(dibenzylideneacetone)dipalladium (8.17 mg, 8.92 μmol),XantPhos (10.3 mg, 17.8 μmol) and4-[5-amino-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(150 mg, 594 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 90° C. overnightwhile vigorously shaking. After cooling to ambient temperature, thereaction mixture was diluted with dichloromethane and concentrated. Itwas redissolved in dimethylsulfoxide, filtered and purified bypreparative HPLC (method 7) to yield the desired product (90 mg, 33%yield).

LC-MS (method 10): R_(t)=1.94 min; MS (ESIpos): m/z=462 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.320 (2.95), 0.331(3.20), 0.440 (2.96), 0.460 (3.12), 1.201 (0.45), 1.212 (0.83), 1.220(0.80), 1.231 (1.29), 1.243 (0.77), 1.250 (0.78), 2.096 (16.00), 2.616(2.95), 2.632 (2.05), 2.671 (0.50), 3.894 (2.66), 3.911 (2.60), 5.755(6.76), 7.898 (2.93), 7.906 (2.85), 7.920 (8.28), 7.932 (4.98), 7.953(1.47), 8.474 (3.37), 8.487 (3.27), 8.627 (0.52), 9.543 (0.66), 10.038(4.00).

Example 2324-[1-(cyclopropylmethyl)-4-methyl-5-{[6-(3-methyl-1H-pyrazolo[4,3-b]pyridin-1-yl)pyrimidin-4-yl]amino}-1H-pyrazol-3-yl]benzonitrile

Under an argon atmosphere,1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazolo[4,3-b]pyridine (161 mg,654 μmol) and sodium phenolate (104 mg, 892 μmol) were suspended in1,4-dioxane (1.7 mL). The reaction mixture was degassed with Ar for 3min. Tris(dibenzylideneacetone)dipalladium (8.17 mg, 8.92 μmol),XantPhos (10.3 mg, 17.8 μmol) and4-[5-amino-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(150 mg, 594 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 90° C. overnightwhile vigorously shaking. After cooling to ambient temperature, thereaction mixture was diluted with dichloromethane and concentrated. Itwas redissolved in dimethylsulfoxide, filtered and purified bypreparative HPLC (method 3) to yield the desired product (196 mg, 71%yield).

LC-MS (method 10): R_(t)=2.11 min; MS (ESIpos): m/z=462 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.318 (3.64), 0.329(3.92), 0.439 (3.57), 0.459 (3.74), 1.199 (0.52), 1.212 (0.97), 1.219(0.97), 1.230 (1.41), 1.248 (0.94), 2.094 (16.00), 2.617 (3.89), 2.671(0.62), 3.890 (3.19), 3.907 (3.18), 5.755 (7.17), 7.341 (0.45), 7.382(0.55), 7.462 (0.83), 7.475 (0.51), 7.580 (1.11), 7.585 (1.64), 7.591(1.33), 7.596 (1.75), 7.606 (1.73), 7.612 (1.40), 7.617 (1.66), 7.790(0.43), 7.898 (1.99), 7.919 (8.20), 7.929 (5.66), 7.950 (1.74), 8.581(0.79), 8.664 (2.61), 8.667 (2.48), 8.674 (2.62), 8.994 (2.19), 9.015(2.18), 9.521 (1.07).

Example 2334-[1-(cyclopropylmethyl)-4-methyl-5-{[6-(3-methyl-1H-pyrazolo[4,3-c]pyridin-1-yl)pyrimidin-4-yl]amino}-1H-pyrazol-3-yl]benzonitrile

Under an argon atmosphere,1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazolo[4,3-c]pyridine (161 mg,654 μmol) and sodium phenolate (104 mg, 892 μmol) were suspended in1,4-dioxane (1.7 mL). The reaction mixture was degassed with Ar for 3min. Tris(dibenzylideneacetone)dipalladium (8.17 mg, 8.92 μmol),XantPhos (10.3 mg, 17.8 μmol) and4-[5-amino-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(150 mg, 594 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 90° C. overnightwhile vigorously shaking. After cooling to ambient temperature, thereaction mixture was diluted with dichloromethane and concentrated. Itwas redissolved in dimethylsulfoxide, filtered and purified bypreparative HPLC (method 7) to yield the desired product (31 mg, 11%yield).

LC-MS (method 10): R_(t)=1.66 min; MS (ESIpos): m/z=462 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (2.97), 0.008(1.60), 0.315 (3.09), 0.327 (3.22), 0.437 (3.16), 0.456 (3.20), 1.195(0.52), 1.208 (0.92), 1.214 (0.89), 1.226 (1.36), 1.245 (0.83), 1.257(0.41), 1.435 (0.46), 2.035 (0.56), 2.089 (16.00), 2.525 (1.53), 2.657(3.01), 2.711 (0.70), 3.888 (2.65), 3.904 (2.50), 5.755 (7.43), 7.382(0.43), 7.461 (0.43), 7.466 (0.44), 7.805 (0.41), 7.898 (1.88), 7.919(8.69), 7.927 (5.13), 7.949 (1.39), 8.539 (1.92), 8.541 (1.89), 8.554(3.79), 8.556 (3.79), 8.583 (6.09), 8.597 (3.45), 9.196 (2.73), 9.548(0.65).

Example 2344-[1-(2,2-difluoroethyl)-5-({6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-yl}amino)-4-methyl-1H-pyrazol-3-yl]benzonitrile

A microwave vial was charged4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (84.8mg, 347 μmol),4-[5-amino-1-(2,2-difluoroethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(100 mg, 381 μmol) and sodium phenolate (44.3 mg, 381 μmol) and thecontents were suspended in 1,4-dioxane (2.5 ml, 29 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (4.13 mg, 4.51 μmol) and Xantphos(6.02 mg, 10.4 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was purified by preparative HPLC (method: column:Reprosil C18; 10 μm; 125×40 mm/flow: 75 mL/min/solvent: A=water (0.1%formic acid), B=acetonitrile/gradient: 0.00-5.50 min=10% B, 17.65-19.48min=95% B, 19.66 min=10% B) to yield the desired product (73.0 mg, 43%).

LC-MS (method 9): R_(t)=1.11 min; MS (ESIpos): m/z=471 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (1.00), 0.006(0.74), 1.078 (1.39), 1.092 (2.81), 1.106 (1.40), 1.989 (0.59), 2.069(16.00), 2.294 (2.37), 3.363 (0.48), 3.377 (1.39), 3.391 (1.37), 3.405(0.46), 4.523 (0.82), 6.258 (0.53), 6.360 (0.54), 6.368 (1.07), 6.375(0.56), 6.477 (0.51), 6.794 (2.54), 7.713 (1.09), 7.822 (2.22), 7.924(13.28), 8.503 (0.57), 9.657 (0.74).

Example 2354-[3-({6-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-yl}amino)-1,4-dimethyl-1H-pyrazol-5-yl]benzonitrile

A microwave vial was charged with4-(3-amino-1,4-dimethyl-1H-pyrazol-5-yObenzonitrile (55.0 mg, 259 μmol),4-chloro-6-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine(79.5 mg, 285 μmol) and sodium phenolate (33.1 mg, 285 μmol) and thecontents were suspended in 1,4-dioxane (0.8 mL). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium(3.56 mg, 3.89 μmol) and XantPhos (4.50 mg, 7.77 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously shaking. After coolingto ambient temperature, the reaction mixture was filtered andconcentrated. The residue was redissolved in dimethylsulfoxide andpurified by preparative HPLC (method 6) to yield the desired product(21.7 mg, 18% yield).

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.75), 0.008(0.72), 1.892 (10.29), 2.288 (14.30), 2.328 (0.55), 2.523 (0.67), 3.743(16.00), 7.461 (0.56), 7.702 (4.28), 7.723 (4.91), 7.901 (1.22), 8.007(4.86), 8.028 (4.62), 8.033 (3.42), 8.164 (1.08), 8.510 (2.45), 9.745(1.38).

Example 2364-[3-({6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-yl}amino)-1,4-dimethyl-1H-pyrazol-5-yl]benzonitrile

A microwave vial was charged with4-(3-amino-1,4-dimethyl-1H-pyrazol-5-yl)benzonitrile (55.0 mg, 259μmol),4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (69.7mg, 285 μmol) and sodium phenolate (33.1 mg, 285 μmol) and the contentswere suspended in 1,4-dioxane (0.8 mL). The reaction mixture wasdegassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (3.56mg, 3.89 μmol) and XantPhos (4.50 mg, 7.77 μmol) were added and thereaction mixture was degassed again for 1 min. The vial was sealed andheated at 85° C. overnight while vigorously shaking. After cooling toambient temperature, the reaction mixture was filtered and concentrated.The residue was redissolved in dimethylsulfoxide and purified bypreparative HPLC (method 1) to yield the desired product (29.8 mg, 27%yield).

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.52), 0.008(0.60), 1.890 (11.52), 2.296 (13.68), 3.747 (16.00), 6.774 (3.85), 7.439(0.91), 7.691 (1.24), 7.704 (4.25), 7.725 (4.89), 7.827 (2.44), 7.963(1.06), 8.007 (4.89), 8.028 (4.25), 8.483 (2.84), 9.637 (1.96).

Example 2374-[5-({6-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-yl}amino)-1-(2-cyclopropylethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile

A microwave vial was charged with4-[5-amino-1-(2-cyclopropylethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(50.0 mg, 188 μmol),4-chloro-6-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine(57.6 mg, 206 μmol) and sodium phenolate (24.0 mg, 206 μmol) and thecontents were suspended in 1,4-dioxane (0.6 mL). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium(2.58 mg, 2.82 μmol) and XantPhos (3.26 mg, 5.63 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously shaking. After coolingto ambient temperature, the reaction mixture was filtered andconcentrated. The residue was redissolved in dimethylsulfoxide andpurified by preparative HPLC (method 8) to yield the desired product(7.5 mg, 8% yield).

LC-MS (method 11): R_(t)=1.62 min; MS (ESIpos): m/z=509 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.058 (3.54), −0.049(3.54), −0.008 (1.29), 0.146 (0.17), 0.306 (2.16), 0.326 (2.29), 0.620(0.86), 1.630 (1.06), 1.647 (2.95), 1.665 (2.85), 1.682 (1.04), 2.061(16.00), 2.280 (1.55), 2.323 (0.95), 2.328 (0.91), 2.346 (0.41), 2.367(0.50), 2.670 (0.48), 2.711 (0.39), 4.040 (1.88), 7.298 (0.19), 7.900(13.30), 8.032 (2.16), 8.164 (0.99), 8.519 (0.35), 9.652 (0.32).

Example 2381-[1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]-2-methylpropan-2-ol

A solution of ethyl[1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]acetate(257 mg, 538 μmol) in tetrahydrofuran (10 ml, 130 mmol) was treated at0° C. with bromo(methyl)magnesium (1.9 ml, 1.0 M in tetrahydrofuran, 1.9mmol). The mixture was stirred 30 min at 0° C. and then allowed to warmup to room temperature. It was left overnight. Additionally 3.5equivalents of bromo(methyl)magnesium (0.63 mL, 1.88 mmol, 3.0 M indiethyl ether) were added and it was stirred one hour at ambienttemperature. The mixture was diluted with saturated aqueous ammoniumchloride solution and extracted with ethyl acetate (3×). The combinedorganic phases were dried over sodium sulfate, concentrated underreduced pressure and the crude product was purified byflash-chromatography on silica gel (dichloromethane/methanol 20:1,column: Biotage SNAP Ultra 10 g) to yield the desired product (75.0 mg,30%).

LC-MS (method 10): R_(t)=2.01 min; MS (ESIpos): m/z=464 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.870 (2.60), 0.889(5.71), 0.908 (2.64), 1.073 (1.43), 1.091 (16.00), 1.108 (1.45), 2.171(9.63), 2.282 (0.71), 2.300 (1.97), 2.319 (1.95), 2.338 (0.69), 2.433(4.17), 2.567 (9.32), 3.357 (0.69), 3.375 (1.49), 3.392 (1.66), 3.409(1.28), 3.649 (11.66), 7.328 (1.84), 7.356 (1.28), 7.378 (2.83), 7.400(1.70), 7.498 (1.68), 7.512 (1.95), 7.519 (1.64), 7.533 (1.26), 8.434(2.44), 9.301 (0.78).

Example 2394-[3-({6-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-yl}amino)-1-(2-cyclopropylethyl)-4-methyl-1H-pyrazol-5-yl]benzonitrile

A microwave vial was charged with4-[3-amino-1-(2-cyclopropylethyl)-4-methyl-1H-pyrazol-5-yl]benzonitrile(44.0 mg, 165 μmol),4-chloro-6-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine(50.7 mg, 182 μmol) and sodium phenolate (21.1 mg, 182 μmol) and thecontents were suspended in 1,4-dioxane (0.5 mL). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium(2.27 mg, 2.48 μmol) and XantPhos (2.87 mg, 4.96 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously shaking. After coolingto ambient temperature, the reaction mixture was filtered andconcentrated. The residue was redissolved in dimethylsulfoxide andpurified by preparative HPLC (method 8) to yield the desired product (8mg, 10% yield).

LC-MS (method 11): R_(t)=1.65 min; MS (ESIpos): m/z=509 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.134 (0.86), −0.123(3.42), −0.120 (3.41), −0.111 (3.65), −0.098 (1.03), −0.008 (2.00),0.008 (2.23), 0.278 (0.91), 0.288 (2.56), 0.291 (2.78), 0.298 (1.55),0.308 (3.12), 0.312 (2.98), 0.322 (1.03), 0.474 (0.70), 0.492 (0.97),0.511 (0.60), 1.563 (1.07), 1.581 (3.15), 1.598 (3.15), 1.614 (1.10),1.886 (10.00), 2.268 (16.00), 2.328 (0.42), 2.523 (0.97), 2.670 (0.43),4.031 (2.14), 4.047 (4.44), 4.064 (2.13), 7.667 (5.53), 7.688 (6.25),7.910 (1.54), 8.007 (6.07), 8.028 (5.44), 8.041 (3.54), 8.173 (1.37),8.521 (3.16), 9.805 (1.84).

Example 2404-[5-({6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-yl}amino)-1,4-dimethyl-1H-pyrazol-3-yl]benzonitrile

A microwave vial was charged with4-(5-amino-1,4-dimethyl-1H-pyrazol-3-yl)benzonitrile (65.0 mg, 306μmol),4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (74.9mg, 306 μmol) and sodium phenolate (39.1 mg, 337 μmol) and the contentswere suspended in 1,4-dioxane (0.95 mL). The reaction mixture wasdegassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (4.21mg, 4.59 μmol) and XantPhos (5.32 mg, 9.19 μmol) were added and thereaction mixture was degassed again for 1 min. The vial was sealed andheated at 85° C. overnight while vigorously shaking. After cooling toambient temperature, the reaction mixture was filtered and concentrated.The residue was redissolved in dimethylsulfoxide and purified bypreparative HPLC (method 1) to yield the desired product (20.4 mg, 16%yield).

LC-MS (method 10): R_(t)=2.03 min; MS (ESIpos): m/z=421 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (2.97), 0.008(2.94), 2.076 (16.00), 2.289 (2.27), 2.327 (0.73), 2.367 (0.53), 2.670(0.53), 2.710 (0.54), 3.701 (7.40), 6.792 (2.54), 7.682 (1.13), 7.818(2.36), 7.900 (12.74), 7.954 (1.10), 8.503 (0.53), 9.639 (0.72).

Example 2414-[5-({6-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-yl}amino)-1,4-dimethyl-1H-pyrazol-3-yl]benzonitrile

A microwave vial was charged with4-(5-amino-1,4-dimethyl-1H-pyrazol-3-yl)benzonitrile (65.0 mg, 306μmol),4-chloro-6-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine(85.5 mg, 306 μmol) and sodium phenolate (39.1 mg, 337 μmol) and thecontents were suspended in 1,4-dioxane (0.95 mL). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium(4.21 mg, 4.59 μmol) and XantPhos (5.32 mg, 9.19 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously shaking. After coolingto ambient temperature, the reaction mixture was filtered andconcentrated. The residue was redissolved in dimethylsulfoxide andpurified by preparative HPLC (method 6) to yield the desired product (17mg, 11% yield).

LC-MS (method 10): R_(t)=2.19 min; MS (ESIpos): m/z=455 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (2.24), 0.008(2.35), 2.073 (16.00), 2.284 (1.89), 2.327 (4.16), 3.700 (6.58), 7.817(0.41), 7.898 (14.12), 7.948 (0.72), 8.014 (0.70), 8.016 (0.78), 8.030(2.17), 8.162 (0.96), 8.527 (0.40), 9.002 (0.68), 9.719 (0.56).

Example 242

N-[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3-methyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged with4-chloro-6-(3-methyl-1H-pyrazol-1-yl)pyrimidine (97.6 mg, 502 μmol) andsodium phenolate (63.5 mg, 547 μmol) and the contents were suspended in1,4-dioxane (1.3 mL). The reaction mixture was degassed with Ar for 3min. Tris(dibenzylideneacetone)dipalladium (6.26 mg, 6.84 μmol),XantPhos (7.92 mg, 13.7 μmol) and4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (100 mg, 456μmol) were added and the reaction mixture was degassed again for 1 min.The vial was sealed and heated at 85° C. overnight while vigorouslyshaking. After cooling to ambient temperature, the reaction mixture wasdiluted with dimethylsulfoxide, filtered and purified by preparativeHPLC (method 3) to yield the desired product (65 mg, 37% yield).

LC-MS (method 10): R_(t)=2.03 min; MS (ESIpos): m/z=378 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.44), 0.008(0.44), 0.871 (3.56), 0.889 (8.34), 0.908 (3.72), 1.647 (0.36), 2.075(0.21), 2.274 (13.93), 2.281 (3.25), 2.289 (1.19), 2.308 (2.66), 2.326(2.62), 2.345 (0.86), 2.670 (0.26), 3.652 (0.42), 3.669 (16.00), 6.386(2.94), 6.392 (2.98), 6.466 (0.35), 6.472 (0.36), 7.149 (0.46), 7.151(0.51), 7.270 (0.41), 7.289 (0.58), 7.292 (0.52), 7.308 (2.25), 7.340(0.32), 7.362 (2.12), 7.367 (0.93), 7.379 (1.20), 7.384 (4.76), 7.401(1.17), 7.406 (2.79), 7.413 (0.37), 7.488 (0.45), 7.493 (0.23), 7.510(2.96), 7.515 (1.23), 7.524 (2.98), 7.532 (2.36), 7.540 (0.93), 7.545(1.96), 8.140 (1.47), 8.437 (2.65), 8.459 (2.70), 8.466 (2.70), 8.540(0.32), 8.546 (0.32), 8.674 (0.33), 8.676 (0.35), 9.432 (2.27).

Example 2434-[1-(cyclopropylmethyl)-4-methyl-5-{[6-(3-methyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-1H-pyrazol-3-yl]benzonitrile

A microwave vial was charged with4-chloro-6-(3-methyl-1H-pyrazol-1-yl)pyrimidine (84.8 mg, 436 μmol) andsodium phenolate (55.2 mg, 476 μmol) and the contents were suspended in1,4-dioxane (1.1 mL). The reaction mixture was degassed with Ar for 3min. Tris(dibenzylideneacetone)dipalladium (6.88 mg, 11.9 μmol),XantPhos (5.44 mg, 5.94 μmol) and4-[5-amino-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(100 mg, 396 μmol), were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously shaking. After cooling to ambient temperature, thereaction mixture was filtered, diluted with dimethylsulfoxide andpurified by preparative HPLC (method 2) to yield the desired product (40mg, 24% yield).

LC-MS (method 10): R_(t)=2.04 min; MS (ESIpos): m/z=411 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.008 (1.05), 0.305(2.67), 0.315 (2.89), 0.429 (2.77), 0.449 (2.99), 1.176 (0.40), 1.189(0.77), 1.195 (0.77), 1.207 (1.13), 1.219 (0.78), 1.226 (0.77), 1.238(0.43), 1.647 (0.52), 2.072 (16.00), 2.260 (2.76), 2.281 (1.57), 3.870(2.38), 3.886 (2.43), 6.405 (2.22), 7.368 (0.43), 7.385 (0.45), 7.398(0.52), 7.893 (1.50), 7.913 (8.38), 7.921 (5.38), 7.943 (1.56), 8.467(4.06), 8.473 (4.03), 9.523 (0.54).

Example 2441-[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]cyclopropanol

Under an argon atmosphere a Schlenk tube was charged with titaniumisopropoxide (300 μl, 1.0 mmol) in tetrahydrofuran (2.0 ml, 25 mmol). At−18° C. ethylmagensium bromide 1.0 M solution in tetrahydrofuran (3.1ml, 1.0 M, 3.1 mmol) was added. The mixture was stirred 30 minutes at−18° C., subsequently a solution of ethyl1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(250 mg, 100% purity, 511 μmol) in 1.5 mL tetrahydrofuran was added andthe resulting mixture was stirred at ambient temperature overnight. Themixture was diluted with saturated aqueous ammonium chloride solutionand water and extracted with ethyl acetate (3×). The combined organicphases were washed with water, brine, dried over sodium sulfate andconcentrated under reduced pressure. The crude product was purified bypreparative HPLC (method: column: Reprosil C18; 10 μm; 125×30 mm/flow:50 mL/min/solvent: A=water (0.01% formic acid), B=acetonitrile/gradient:0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75 min=100% B, 19.75-23.00min=90% B) and subsequent flash-chromatography on silica gel to yield44.2 mg (18%) of the desired product along with(±)-1-[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]propan-1-ol(racemic) (41.5 mg, 16%).

LC-MS (method 9): R_(t)=1.03 min; MS (ESIpos): m/z=474 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.289 (2.61), 0.300(2.83), 0.420 (2.56), 0.439 (2.71), 0.648 (3.43), 0.930 (1.45), 0.941(3.86), 0.957 (1.27), 1.158 (1.74), 1.176 (3.65), 1.193 (2.48), 1.211(0.69), 1.989 (5.99), 2.004 (14.99), 2.262 (3.44), 2.714 (16.00), 3.826(2.54), 3.843 (2.51), 4.003 (0.47), 4.021 (1.36), 4.039 (1.35), 4.057(0.45), 5.479 (4.01), 7.252 (2.08), 7.274 (4.26), 7.296 (2.32), 7.714(1.64), 7.728 (2.16), 7.733 (2.12), 7.748 (1.54), 8.467 (0.77), 9.361(0.72).

Example 245N-[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged with4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (80.0 mg, 365μmol), 4-chloro-6-(1H-pyrazol-1-yl)pyrimidine (72.5 mg, 401 μmol) andsodium phenolate (46.6 mg, 401 μmol) and the contents were suspended in1,4-dioxane (1.0 mL). The reaction mixture was degassed with Ar for 3min. Tris(dibenzylideneacetone)dipalladium (4.34 mg, 4.74 μmol) andXantPhos (6.33 mg, 10.9 μmol) were added and the reaction mixture wasdegassed again for 1 min. The vial was sealed and heated at 85° C.overnight while vigorously shaking. After cooling to ambienttemperature, the reaction mixture was concentrated and purified by flashcolumn chromatography (SNAP Ultra 25 g, cyclohexane/ethyl acetategradient 90/10 to 40/60) to yield the desired product (57 mg, 42%yield).

LC-MS (method 10): R_(t)=1.95 min; MS (ESIpos): m/z=364 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.53), −0.008(8.13), 0.008 (4.15), 0.014 (0.56), 0.146 (0.52), 0.869 (3.68), 0.888(8.25), 0.906 (3.57), 2.296 (1.03), 2.314 (2.75), 2.333 (2.92), 2.351(0.81), 2.367 (0.52), 2.524 (2.54), 2.670 (0.61), 2.710 (0.50), 3.665(16.00), 6.578 (2.31), 6.582 (2.49), 6.585 (2.51), 6.589 (2.17), 7.360(2.14), 7.366 (1.03), 7.382 (4.65), 7.405 (2.87), 7.425 (1.79), 7.509(2.69), 7.514 (1.29), 7.522 (2.98), 7.531 (2.32), 7.539 (1.06), 7.545(1.94), 7.856 (2.75), 7.859 (2.66), 8.482 (2.39), 8.587 (2.60), 8.592(2.45), 8.594 (2.37), 9.524 (2.63).

Example 2464-[1-(cyclopropylmethyl)-4-methyl-5-{[6-(1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-1H-pyrazol-3-yl]benzonitrile

A microwave vial was charged with4-[5-amino-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(80.0 mg, 317 μmol), 4-chloro-6-(1H-pyrazol-1-yl)pyrimidine (63.0 mg,349 μmol) and sodium phenolate (40.5 mg, 349 μmol) and the contents weresuspended in 1,4-dioxane (0.9 mL). The reaction mixture was degassedwith Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (3.77 mg, 4.12μmol) and XantPhos (5.50 mg, 9.51 μmol) were added and the reactionmixture was degassed again for 1 min. The vial was sealed and heated at85° C. overnight while vigorously shaking. After cooling to ambienttemperature, the reaction mixture was concentrated and purified by flashcolumn chromatography (SNAP Ultra 25 g, cyclohexane/ethyl acetategradient 90/10 to 40/60) to yield the desired product (27 mg, 21%yield).

LC-MS (method 10): R_(t)=1.95 min; MS (ESIpos): m/z=397 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.28), −0.008(3.77), 0.008 (2.72), 0.146 (0.29), 0.300 (2.23), 0.311 (2.29), 0.422(2.26), 0.442 (2.28), 1.157 (0.26), 1.175 (0.61), 1.193 (0.76), 1.202(0.87), 1.234 (0.44), 1.989 (0.47), 2.036 (0.43), 2.069 (16.00), 2.328(0.29), 2.367 (0.25), 2.524 (1.23), 2.670 (0.31), 2.710 (0.26), 3.875(2.12), 3.892 (2.01), 5.754 (2.21), 6.595 (1.92), 7.855 (0.59), 7.890(1.56), 7.912 (8.79), 7.918 (6.26), 7.940 (1.05), 8.508 (0.38), 8.593(2.77), 8.599 (2.72), 9.616 (0.65).

Example 2474-[1-(cyclopropylmethyl)-4-methyl-5-({6-[4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidin-4-yl}amino)-1H-pyrazol-3-yl]benzonitrile

A microwave vial was charged with4-[5-amino-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(80.0 mg, 317 μmol),4-chloro-6-[4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidine (140 mg, 62%purity, 349 μmol) and sodium phenolate (40.5 mg, 349 μmol) and thecontents were suspended in 1,4-dioxane (0.9 mL). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium(3.77 mg, 4.12 μmol) and XantPhos (5.50 mg, 9.51 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously shaking. After coolingto ambient temperature, the reaction mixture was concentrated and theresidue purified by flash column chromatography (KP Sil 25g,cyclohexane/ethyl acetate gradient 90/10 to 40/60) to yield the desiredproduct (37 mg, 24% yield).

LC-MS (method 10): R_(t)=2.26 min; MS (ESIpos): m/z=465 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (1.09), −0.008(9.41), 0.008 (9.55), 0.146 (1.07), 0.310 (1.92), 0.424 (1.87), 0.445(1.89), 1.193 (0.75), 1.434 (0.32), 1.988 (0.69), 2.069 (16.00), 2.327(1.17), 2.366 (0.83), 2.669 (1.23), 2.710 (0.93), 3.879 (1.57), 5.754(3.55), 7.912 (9.25), 8.343 (0.29), 8.552 (0.29), 9.185 (3.33), 9.768(0.32).

Example 2484-[1-(2,2-difluoroethyl)-5-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-4-methyl-1H-pyrazol-3-yl]benzonitrile

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (72.3 mg, 347 μmol),4-[5-amino-1-(2,2-difluoroethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(100 mg, 381 μmol) and sodium phenolate (44.3 mg, 381 μmol) and thecontents were suspended in 1,4-dioxane (2.5 ml, 29 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (4.13 mg, 4.51 μmol) and Xantphos(6.02 mg, 10.4 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was filtered and purified by preparative HPLC (method3) to yield the desired product (64.0 mg, 38%).

LC-MS (method 10): R_(t)=2.05 min; MS (ESIpos): m/z=435 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.20), 0.008(1.44), 2.065 (11.96), 2.183 (4.62), 2.633 (10.27), 2.654 (1.02), 4.477(0.51), 4.513 (0.94), 4.545 (0.51), 6.154 (2.42), 6.228 (0.50), 6.356(0.47), 6.365 (0.99), 6.374 (0.50), 6.502 (0.46), 7.921 (16.00), 8.469(1.04), 9.481 (1.76).

Example 249(±)-1-[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]ethanol(racemic)

A solution of1-[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]ethanone(51.9 mg, 113 μmol) in methanol (2.0 ml, 49 mmol) was treated withsodium borohydride (2.14 mg, 56.5 μmol). The mixture was stirred 30minutes at ambient temperature. The mixture was diluted with 1 mL waterand purified by preparative HPLC (method: column: Reprosil C18; 10 μm;125×30 mm/flow: 50 mL/min/solvent: A=water (0.01% formic acid),B=acetonitrile/gradient: 0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75min=100% B, 19.75-23.00 min=90% B) and subsequently byflash-chromatography on silica gel (column: SNAP KP-Sil 10 g,dichloromethane/ethyl acetate) to yield 17.1 mg (33%) of the desiredproduct.

LC-MS (method 11): R_(t)=1.32 min; MS (ESIpos): m/z=462 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.63), 0.008(0.77), 0.291 (2.36), 0.302 (2.61), 0.420 (2.30), 0.440 (2.46), 1.175(0.85), 1.182 (0.66), 1.194 (1.04), 1.206 (0.63), 1.212 (0.64), 1.232(0.52), 1.320 (4.71), 1.336 (4.82), 2.003 (14.03), 2.234 (2.91), 2.631(16.00), 3.824 (2.35), 3.841 (2.31), 4.765 (0.79), 4.773 (0.87), 4.782(0.83), 4.789 (0.85), 4.909 (2.09), 4.916 (1.97), 5.754 (0.71), 7.251(2.08), 7.273 (4.26), 7.295 (2.30), 7.712 (1.53), 7.726 (1.98), 7.732(1.91), 7.746 (1.43), 8.453 (0.70), 9.345 (0.74).

Example 250N-[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-[4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidin-4-amine

A microwave vial was charged with4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (160 mg, 730μmol), 4-chloro-6-[4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidine (322mg, 62% purity, 803 μmol) and sodium phenolate (93.2 mg, 803 μmol) andthe contents were suspended in 1,4-dioxane (2.1 mL). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (8.69 mg, 9.49 μmol) and XantPhos(12.7 mg, 21.9 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously shaking. After cooling to ambient temperature, thereaction mixture was concentrated and the residue purified by flashcolumn chromatography (SNAP Ultra 25 g, cyclohexane/ethyl acetategradient 90/10 to 40/60) to yield the desired product (144 mg, 43%yield).

LC-MS (method 10): R_(t)=2.31 min; MS (ESIpos): m/z=432 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.37), 0.008(1.45), 0.774 (0.35), 0.844 (0.32), 0.852 (0.20), 0.870 (3.53), 0.889(8.09), 0.907 (3.54), 1.235 (0.26), 1.398 (1.58), 2.303 (0.77), 2.322(2.24), 2.340 (2.13), 2.359 (0.70), 2.671 (0.20), 2.711 (0.16), 3.642(0.45), 3.666 (16.00), 3.752 (0.58), 3.784 (0.65), 5.755 (0.82), 7.330(0.17), 7.354 (0.28), 7.361 (2.00), 7.366 (0.81), 7.383 (4.57), 7.400(1.00), 7.406 (2.80), 7.421 (0.40), 7.443 (0.23), 7.511 (3.21), 7.516(1.93), 7.524 (3.44), 7.533 (2.65), 7.541 (1.13), 7.546 (2.17), 7.584(0.25), 7.598 (0.19), 7.815 (0.36), 7.818 (0.37), 8.332 (3.69), 8.405(0.35), 8.414 (0.21), 8.549 (2.43), 8.951 (0.32), 8.953 (0.33), 9.162(2.92), 9.307 (0.27), 9.730 (1.36).

Example 2514-[1-(2,2-difluoroethyl)-3-({6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-yl}amino)-4-methyl-1H-pyrazol-5-yl]benzonitrile

A microwave vial was charged4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (73.8mg, 302 μmol),4-[3-amino-1-(2,2-difluoroethyl)-4-methyl-1H-pyrazol-5-yl]benzonitrile(87.0 mg, 332 μmol) and sodium phenolate (38.5 mg, 332 μmol) and thecontents were suspended in 1,4-dioxane (2.2 ml, 25 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (3.59 mg, 3.92 μmol) and Xantphos(5.23 mg, 9.05 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with water and filtered over a colum withExtrelut and silica gel (solvent: dichloromethane/ethyl acetate 20:1).The filtrate was concentrated under reduced pressure and the crudeproduct was purified by preparative HPLC (method: column: Reprosil C18;10 μm; 125×40 mm/flow: 75 mL/min/solvent: A=water (0.1% formic acid),B=acetonitrile/gradient: 0.00-5.50 min=10% B, 17.65-19.48 min=95% B,19.66 min=10% B) to yield 36.0 mg (25%) of the desired product.

LC-MS (method 10): R_(t)=2.12 min; MS (ESIpos): m/z=471 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.90), 0.008(0.90), 1.073 (0.47), 1.091 (0.95), 1.109 (0.47), 1.883 (13.58), 2.292(16.00), 3.375 (0.51), 3.392 (0.50), 4.414 (1.05), 4.423 (1.16), 4.450(2.18), 4.459 (2.22), 4.487 (1.12), 4.496 (1.02), 6.158 (0.75), 6.285(0.73), 6.295 (1.53), 6.304 (0.73), 6.432 (0.69), 6.777 (4.65), 7.573(0.70), 7.663 (5.08), 7.684 (5.92), 7.691 (1.91), 7.828 (2.91), 7.964(1.24), 8.022 (5.69), 8.043 (5.13), 8.508 (3.79), 9.787 (3.25).

Example 2524-[1-(2,2-difluoroethyl)-3-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-4-methyl-1H-pyrazol-5-yl]benzonitrile

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (62.9 mg, 302 μmol),4-[3-amino-1-(2,2-difluoroethyl)-4-methyl-1H-pyrazol-5-yl]benzonitrile(87.0 mg, 332 μmol) and sodium phenolate (38.5 mg, 332 μmol) and thecontents were suspended in 1,4-dioxane (2.2 ml, 25 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (3.59 mg, 3.92 μmol) and Xantphos(5.23 mg, 9.05 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was filtered and purified by preparative HPLC (method3) to yield the desired product (56.0 mg, 38%).

LC-MS (method 10): R_(t)=2.01 min; MS (ESIpos): m/z=435 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.647 (0.48), 1.879(15.67), 2.074 (3.82), 2.182 (15.31), 2.502 (16.00), 2.625 (14.92),4.401 (1.18), 4.410 (1.27), 4.437 (2.41), 4.446 (2.43), 4.474 (1.24),4.482 (1.13), 6.136 (4.01), 6.156 (0.79), 6.284 (0.76), 6.293 (1.52),6.302 (0.75), 6.430 (0.71), 7.383 (0.41), 7.531 (1.64), 7.657 (4.75),7.678 (5.11), 8.019 (4.94), 8.039 (4.21), 8.475 (3.99), 9.580 (4.53).

Example 2536-(3,5-dimethyl-1H-pyrazol-1-yl)-N-[5-(4-fluorophenyl)-4-methoxy-1-methyl-1H-pyrazol-3-yl]pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (49.7 mg, 238 μmol),5-(4-fluorophenyl)-4-methoxy-1-methyl-1H-pyrazol-3-amine (58.0 mg, 262μmol) and sodium phenolate (30.4 mg, 262 μmol) and the contents weresuspended in 1,4-dioxane (1.7 ml, 20 mmol). The reaction mixture wasdegassed with Ar for 3 min. Tris(dibenzylidenaceton)dipalladium (2.84mg, 3.10 μmol) and Xantphos (4.14 mg, 7.15 μmol) were added and thereaction mixture was degassed again for 1 min. The vial was sealed andheated at 85° C. overnight while vigorously stirring. After cooling toambient temperature, the reaction mixture was purified by preparativeHPLC (method: column: Reprosil C18; 10 μm; 125×40 mm/flow: 75mL/min/solvent: A=water (0.1% formic acid), B=acetonitrile/gradient:0.00-5.50 min=10% B, 17.65-19.48 min=95% B, 19.66 min=10% B) to yieldthe desired product (35.5 mg, 36%).

LC-MS (method 10): R_(t)=1.98 min; MS (ESIpos): m/z=394 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.074 (1.05), 2.176(11.46), 2.227 (0.49), 2.623 (10.61), 2.663 (0.45), 3.531 (16.00), 3.718(13.08), 6.130 (3.01), 7.205 (3.65), 7.207 (3.61), 7.364 (1.63), 7.386(3.53), 7.408 (1.97), 7.592 (2.00), 7.597 (0.96), 7.606 (2.26), 7.614(1.95), 7.623 (0.83), 7.628 (1.65), 8.448 (2.88), 9.368 (2.12).

Example 2546-(3,5-dimethyl-1H-pyrazol-1-yl)-N-[3-(4-fluorophenyl)-4-methoxy-1-methyl-1H-pyrazol-5-yl]pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (39.4 mg, 189 μmol),3-(4-fluorophenyl)-4-methoxy-1-methyl-1H-pyrazol-5-amine (46.0 mg, 208μmol) and sodium phenolate (24.1 mg, 208 μmol) and the contents weresuspended in 1,4-dioxane (1.3 ml, 16 mmol). The reaction mixture wasdegassed with Ar for 3 min. Tris(dibenzylidenaceton)dipalladium (2.25mg, 2.46 μmol) and Xantphos (3.28 mg, 5.67 μmol) were added and thereaction mixture was degassed again for 1 min. The vial was sealed andheated at 85° C. overnight while vigorously stirring. After cooling toambient temperature, the reaction mixture was purified by preparativeHPLC (method: column: Reprosil C18; 10 μm; 125×40 mm/flow: 75mL/min/solvent: A=water (0.1% formic acid), B=acetonitrile/gradient:0.00-5.50 min=10% B, 17.65-19.48 min=95% B, 19.66 min=10% B) to yieldthe desired product (32.5 mg, 43%).

LC-MS (method 10): R_(t)=2.04 min; MS (ESIpos): m/z=394 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.84), 0.008(0.92), 1.091 (0.45), 2.174 (4.04), 2.635 (10.22), 3.615 (8.71), 3.683(16.00), 6.151 (2.30), 7.236 (1.68), 7.258 (3.44), 7.281 (1.81), 7.868(1.52), 7.882 (1.74), 7.890 (1.70), 7.904 (1.46), 8.494 (1.20), 9.464(1.41).

Example 2554-(3-{[6-(4-bromo-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-1,4-dimethyl-1H-pyrazol-5-yl)benzonitrile

4-(3-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-1,4-dimethyl-1H-pyrazol-5-yl)benzonitrile(84.0 mg, 218 μmol) was dissolved in acetonitrile,1-bromopyrrolidine-2,5-dione (46.7 mg, 262 μmol) was added at ambienttemperature and the reaction mixture stirred overnight. Water was addedand the mixture stirred for further 5 min. The precipitated solid wascollected by filtration, washed with water and dried overnight in avacuum drying-oven at 40° C. The filtrate was extracted with ethylacetate, the organic phase extract was dried over sodium sulfate andconcentrated. Both solids were combined and lyophilized fromacetonitrile/water. It was further purified by preparative HPLC (method2) to yield the desired product (12 mg, 12% yield).

LC-MS (method 10): R_(t)=2.25 min; MS (ESIpos): m/z=463 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.887 (12.71), 2.221(14.72), 2.653 (16.00), 2.670 (0.45), 3.736 (15.81), 7.415 (1.20), 7.698(4.27), 7.719 (4.76), 8.004 (4.72), 8.025 (3.98), 8.491 (2.64), 9.553(2.35).

Example 2561-{[1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]methyl}cyclopropanol

Under an argon atmosphere a Schlenk tube was charged with a ethyl[1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]acetate(235 mg, 90% purity, 443 μmol) in tetrahydrofuran (2.0 ml, 25 mmol).Titanium isopropoxylate (140 μl, 490 μmol) and ethylmagnesium bromide(1.6 ml, 1.0 M in tetrahydrofuran, 1.6 mmol) were added at 0° C. Themixture was stirred 2 hours at 0° C. and overnight at ambienttemperature. The mixture was diluted with saturated ammonium chloridesolution. The occurring precipitate was filtered off. The filtrate wasextracted with ethyl acetate (3×). The combined organic phases werewashed with brine, dried over sodium sulfate and concentrated underreduced pressure. The crude product was purified by preparative HPLC(method: column: Reprosil C18; 10 μm; 125×40 mm/flow: 75 mL/min/solvent:A=water (0.1% formic acid), B=acetonitrile/gradient: 0.00-5.50 min=10%B, 17.65-19.48 min=95% B, 19.66 min=10% B) to yield 5.5 mg (3%) of thedesired product along with propan-2-yl[1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]acetateas by-product.

LC-MS (method 10): R_(t)=1.96 min; MS (ESIpos): m/z=462 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.343 (1.14), 0.353(3.37), 0.357 (3.13), 0.365 (1.40), 0.509 (1.25), 0.517 (3.14), 0.521(2.85), 0.531 (0.93), 0.876 (3.50), 0.891 (7.88), 0.906 (3.46), 2.172(0.44), 2.186 (13.76), 2.290 (0.75), 2.305 (2.13), 2.320 (2.05), 2.334(0.65), 2.583 (14.04), 2.657 (5.30), 3.651 (16.00), 5.221 (5.06), 7.319(1.96), 7.361 (2.11), 7.366 (0.78), 7.375 (1.02), 7.379 (4.46), 7.384(0.91), 7.393 (0.85), 7.397 (2.53), 7.503 (2.47), 7.507 (1.04), 7.514(2.70), 7.520 (2.17), 7.527 (0.84), 7.531 (1.87), 8.432 (2.96), 8.434(2.87), 9.285 (2.09).

Example 257 ethyl[1-(6-{[1-(4-cyanophenyl)-3,5-dimethyl-1H-pyrazol-4-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]acetate

A microwave vial was charged4-(4-amino-3,5-dimethyl-1H-pyrazol-1-yl)benzonitrile (250 mg, 1.18mmol), ethyl[1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]acetate (382mg, 1.30 mmol) and sodium phenolate (150 mg, 1.30 mmol) and the contentswere suspended in 1,4-dioxane (5.0 ml, 58 mmol). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylidenaceton)dipalladium(32.4 mg, 35.3 μmol) and Xantphos (40.9 mg, 70.7 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously stirring. After coolingto ambient temperature, the reaction mixture was diluted with 1.0 Mhydrochloric acid and extracted with ethyl acetate (2×). The combinedorganic phases were dried over Extrelut NT3 and concentrated underreduced pressure. The crude product was recrystallized from acetonitrileto yield the desired product (82.0 mg, 43%).

LC-MS (method 10): R_(t)=1.90 min; MS (ESIpos): m/z=471 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.166 (3.51), 1.183(7.23), 1.201 (3.62), 1.647 (0.80), 2.086 (0.67), 2.107 (16.00), 2.131(2.04), 2.294 (10.13), 2.566 (13.92), 3.470 (4.27), 3.887 (1.43), 4.048(1.03), 4.066 (3.02), 4.083 (2.99), 4.101 (1.00), 7.367 (0.59), 7.384(0.60), 7.397 (0.72), 7.811 (1.64), 7.831 (2.02), 7.978 (3.67), 7.999(2.86), 8.078 (0.41), 8.406 (0.52), 8.940 (2.67).

Example 258 ethyl1-(6-{[3-(4-cyanophenyl)-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate

A microwave vial was charged with4-[5-amino-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(103 mg, 409 μmol), ethyl1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate (120 mg,450 μmol) and sodium phenolate (52.2 mg, 450 μmol) and the contents weresuspended in 1,4-dioxane (1.2 mL). The reaction mixture was degassedwith Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (4.87 mg, 5.32μmol) and XantPhos (7.10 mg, 12.3 μmol) were added and the reactionmixture was degassed again for 1 min. The vial was sealed and heated at85° C. overnight while vigorously shaking. After cooling to ambienttemperature, the reaction mixture was filtered and concentrated. Theresidue was redissolved in dimethylsulfoxide and purified by preparativeHPLC (method 3) to yield the desired product (23 mg, 11% yield).

LC-MS (method 10): R_(t)=2.07 min; MS (ESIpos): m/z=483 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.44), 0.008(0.48), 0.302 (2.29), 0.313 (2.48), 0.432 (2.56), 0.452 (2.70), 1.186(0.77), 1.199 (6.89), 1.217 (14.07), 1.235 (6.88), 1.288 (0.54), 1.306(1.10), 1.323 (0.56), 2.073 (16.00), 2.263 (2.56), 2.328 (0.43), 2.708(1.37), 3.873 (2.31), 3.890 (2.29), 4.246 (2.12), 4.264 (6.78), 4.282(6.75), 4.299 (2.14), 4.308 (0.60), 4.326 (0.51), 6.753 (2.19), 6.846(0.41), 7.281 (0.41), 7.300 (0.48), 7.345 (0.60), 7.887 (1.41), 7.909(9.94), 7.916 (6.20), 7.938 (1.10), 8.428 (0.43), 8.794 (0.41).

Example 259 ethyl4-chloro-1-(6-{[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate

A microwave vial was charged with5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-amine (74.4 mg, 362 μmol),ethyl4-chloro-1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate(120 mg, 398 μmol) and sodium phenolate (46.3 mg, 398 μmol) and thecontents were suspended in 1,4-dioxane (1.0 mL). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium(4.31 mg, 4.71 μmol) and XantPhos (6.29 mg, 10.9 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously shaking. After coolingto ambient temperature, the reaction mixture was filtered andconcentrated. The residue was redissolved in dimethylsulfoxide andpurified by preparative HPLC (method 3) to yield the desired product(10.5 mg, 6% yield).

LC-MS (method 10): R_(t)=2.29 min; MS (ESIpos): m/z=470 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.19), 0.008(1.15), 1.228 (4.97), 1.246 (10.73), 1.264 (5.10), 1.304 (0.71), 1.322(1.55), 1.340 (0.77), 1.863 (11.32), 2.281 (15.27), 2.323 (0.51), 2.328(0.62), 2.366 (0.27), 2.668 (2.83), 2.692 (0.38), 2.710 (0.27), 3.688(2.96), 3.696 (16.00), 4.322 (1.68), 4.340 (5.36), 4.358 (5.30), 4.375(1.63), 7.359 (2.49), 7.364 (1.32), 7.381 (5.27), 7.403 (3.00), 7.515(3.04), 7.521 (1.35), 7.529 (3.29), 7.537 (2.69), 7.546 (1.04), 7.551(2.29), 8.424 (2.32), 8.573 (0.29), 9.720 (1.33).

Example 260

N-[3-(4-bromophenyl)-1,4-dimethyl-1H-pyrazol-5-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

In a microwave vial, 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine(400 mg, 1.92 mmol) and3-(4-bromophenyl)-1,4-dimethyl-1H-pyrazol-5-amine (561 mg, 2.11 mmol)were dissolved in N-methylpyrrolidone (2.5 mL) and a solution ofhydrochloric acid in 1,4-dioxane (1.9 ml, 4.0 M, 7.7 mmol) was added.The vial was sealed and irradiated in a microwave at 190° C. for 2 hwhile stirring. The mixture was diluted with acetonitrile and water andpurified by preparative HPLC (column: Chromatorex C18; 250*40 mm, 10 μM,flow 100 mL/min, gradient acetonitrile/water (containing 0.1%trifluoroacetic acid) 10/90 to 95/5) to yield the desired product (312mg, 36% yield).

LC-MS (method 9): R_(t)=1.17 min; MS (ESIpos): m/z=438 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.025 (16.00), 2.073(0.53), 2.174 (4.49), 2.630 (14.25), 2.670 (0.52), 3.665 (11.59), 6.146(3.12), 7.614 (1.35), 7.635 (8.18), 7.644 (6.80), 7.666 (1.19), 8.469(1.04), 9.420 (2.40).

Example 2612-[4-chloro-1-(6-{[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3-methyl-1H-pyrazol-5-yl]propan-2-ol

Under an argon atmosphere, ethyl4-chloro-1-(6-{[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate(9.00 mg, 19.2 μmol) was dissolved in tetrahydrofuran and the solutioncooled to 0° C. A solution of bromo(methyl)magnesium (96 μl, 1.0 M, 96μmol) was added dropwise and the reaction mixture was stirred for 4 h atambient temperature. A seond aliquot of bromo(methyl)magnesium (96 μl,1.0 M in tetrahydrofuran, 96 μmol) was added and the reaction mixturewas stirred at ambient temperature overnight. The reaction mixture wascarefully quenched by addition of water and extracted withdichloromethane (3×). The combined organic phase extracts were driedover magnesium sulfate and concentrated. The residue was purified byflash column chromatography (SNAP Ultra 10 g, cyclohexane/ethyl acetategradient 95/5 to 5/95) to yield the desired product (2.0 mg, 21% yield).

LC-MS (method 10): R_(t)=2.21 min; MS (ESIpos): m/z=456 [M+H]⁺

Example 2622-[1-(6-{[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3-methyl-1H-pyrazol-5-yl]propan-2-ol

Under an argon atmosphere, ethyl1-(6-{[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate(7.80 mg, 17.9 μmol) was dissolved in tetrahydrofuran (0.7 mL) and thesolution cooled to 0° C. A solution of bromo(methyl)magnesium (90 μl,1.0 M, 90 μmol) was added dropwise and the reaction mixture was stirredfor 4 h at ambient temperature. A seond aliquot ofbromo(methyl)magnesium (90 μl, 1.0 M, 90 μmol) was added and thereaction mixture was stirred at ambient temperature overnight. Thereaction mixture was carefully quenched by addition of water andextracted with dichloromethane (3×). The combined organic phase extractswere dried over magnesium sulfate and concentrated. The residue waspurified by flash column chromatography (SNAP Ultra 10 g,cyclohexane/ethyl acetate gradient 95/5 to 5/95) to yield the desiredproduct (2.5 mg, 32% yield).

LC-MS (method 10): R_(t)=1.96 min; MS (ESIpos): m/z=422 [M+H]⁺

Example 2634-[1-(cyclopropylmethyl)-5-({6-[5-(2-hydroxypropan-2-yl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-yl}amino)-4-methyl-1H-pyrazol-3-yl]benzonitrile

Under an argon atmosphere, ethyl1-(6-{[3-(4-cyanophenyl)-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate(21.0 mg, 43.5 μmol) was dissolved in tetrahydrofuran and the solutioncooled to 0° C. A solution of bromo(methyl)magnesium (220 μl, 1.0 M intetrahydrofuran, 220 μmol) was added dropwise and the reaction mixturewas stirred for 4 h at ambient temperature. A seond aliquot ofbromo(methyl)magnesium (220 μl, 1.0 M in tetrahydrofuran, 220 μmol) wasadded and the reaction mixture was stirred at ambient temperatureovernight. The reaction mixture was carefully quenched by addition ofwater and extracted with dichloromethane (3×). The combined organicphase extracts were dried over magnesium sulfate and concentrated. Theresidue was purified by flash column chromatography (SNAP Ultra 10 g,cyclohexane/ethyl acetate gradient 95/5 to 5/95) to yield the desiredproduct (5.0 mg, 23% yield).

LC-MS (method 10): R_(t)=2.01 min; MS (ESIpos): m/z=469 [M+H]⁺

Example 2642-[1-(6-{[4-ethyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3-methyl-1H-pyrazol-5-yl]propan-2-ol

Under an argon atmosphere, ethyl1-(6-{[4-ethyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate(44.0 mg, 97.9 μmol) was dissolved in tetrahydrofuran (2.0 mL) and thesolution cooled to 0° C. A solution of bromo(methyl)magnesium (490 μl,1.0 M in tetrahydrofuran, 490 μmol) was added dropwise and the reactionmixture was stirred for 4 h at ambient temperature. A seond aliquot ofbromo(methyl)magnesium (490 μl, 1.0 M in tetrahydrofuran, 490 μmol) wasadded and the reaction mixture was stirred at ambient temperatureovernight. The reaction mixture was carefully quenched by addition ofwater and extracted with dichloromethane (3×). The combined organicphase extracts were dried over magnesium sulfate and concentrated. Theresidue was purified by flash column chromatography (SNAP Ultra 10 g,cyclohexane/ethyl acetate gradient 95/5 to 5/95) to yield the desiredproduct (19 mg, 45% yield).

LC-MS (method 10): R_(t)=1.98 min; MS (ESIpos): m/z=436 [M+H]⁺

Example 2656-(4-bromo-3,5-dimethyl-1H-pyrazol-1-yl)-N-[4-ethyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]pyrimidin-4-amine

Under an argon atmosphere, a round-bottom flask was charged with4-ethyl-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-amine (1.00 g, 4.56mmol), 4-(4-bromo-3,5-dimethyl-1H-pyrazol-1-yl)-6-chloropyrimidine (1.19g, 4.15 mmol) and sodium phenolate (529 mg, 4.56 mmol) and the contentswere suspended in 1,4-dioxane (12 mL). The reaction mixture was degassedwith Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (49.4 mg, 53.9μmol) and XantPhos (72.0 mg, 124 μmol) were added and the reactionmixture was degassed again for 1 min. The reaction mixture was heated at85° C. overnight while vigorously stirring. After cooling to ambienttemperature, the reaction mixture was diluted with water and extractedwith ethyl acetate. The organic phase extract was dried over sodiumsulfate and concentrated. The residue purified by flash columnchromatography (SNAP Ultra 50g, cyclohexane/ethyl acetate gradient 98/12to 0/100). to yield the desired product (969 mg, 45% yield).

LC-MS (method 10): R_(t)=2.47 min; MS (ESIpos): m/z=470 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.26), −0.008(2.20), 0.008 (1.95), 0.146 (0.25), 0.966 (3.51), 0.985 (7.95), 1.004(3.66), 1.157 (0.47), 1.175 (1.00), 1.193 (0.49), 1.398 (0.56), 1.988(1.79), 2.211 (2.46), 2.328 (0.39), 2.366 (0.22), 2.442 (0.68), 2.461(1.99), 2.480 (2.13), 2.663 (16.00), 2.710 (0.24), 3.568 (0.18), 3.638(9.64), 4.021 (0.42), 4.038 (0.43), 7.247 (1.94), 7.269 (4.02), 7.291(2.25), 7.648 (1.36), 7.662 (1.79), 7.683 (1.34), 8.508 (0.65), 9.467(0.78).

Example 2664-(5-{[6-(4-fluoro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-4-methyl-1H-pyrazol-3-yl)benzonitrile

A microwave vial was charged with4-(3-amino-4-methyl-1H-pyrazol-5-yl)benzonitrile (63.6 mg, 321 μmol),4-chloro-6-(4-fluoro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (80.0 mg,353 μmol) and sodium phenolate (41.0 mg, 353 μmol) and the contents weresuspended in 1,4-dioxane (0.9 mL). The reaction mixture was degassedwith Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (3.82 mg, 4.17μmol) and XantPhos (5.57 mg, 9.63 μmol) were added and the reactionmixture was degassed again for 1 min. The vial was sealed and heated at85° C. overnight while vigorously shaking. After cooling to ambienttemperature, the reaction mixture was filtered and concentrated. Theresidue was redissolved in dimethylsulfoxide and purified by preparativeHPLC (XBridge C18 5 μm 100×30 mm, solvent A: water, solvent B:acetonitrile, flow: 65 mL/min plus 5 mL 2% formic acid in water,gradient 0-2 min: 20% B, 2-7 min: to 92% B, 7-9 min: 92% B) to yield thedesired product (3.8 mg, 3% yield).

LC-MS (method 10): R_(t)=1.97 min; MS (ESIpos): m/z=389 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (1.01), −0.008(7.45), 0.008 (6.99), 0.146 (1.01), 1.646 (0.64), 2.112 (13.79), 2.208(16.00), 2.327 (3.13), 2.366 (1.20), 2.592 (11.03), 2.596 (12.69), 2.670(3.59), 2.710 (1.20), 7.385 (0.64), 7.468 (1.20), 7.797 (4.32), 7.818(5.70), 7.908 (2.30), 7.973 (5.70), 7.994 (4.51), 8.474 (3.13), 8.509(0.83), 9.522 (3.31), 9.658 (0.46), 13.115 (2.85).

Example 2676-(4-fluoro-3,5-dimethyl-1H-pyrazol-1-yl)-N-[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]pyrimidin-4-amine

A microwave vial was charged with5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-amine (85.0 mg, 414 μmol),4-chloro-6-(4-fluoro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (103 mg,456 μmol) and sodium phenolate (52.9 mg, 456 μmol) and the contents weresuspended in 1,4-dioxane (1.2 mL). The reaction mixture was degassedwith Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (4.93 mg, 5.38μmol) and XantPhos (7.19 mg, 12.4 μmol) were added and the reactionmixture was degassed again for 1 min. The vial was sealed and heated at85° C. overnight while vigorously shaking. After cooling to ambienttemperature, the reaction mixture was filtered and concentrated. Theresidue was redissolved in dimethylsulfoxide and purified by preparativeHPLC (method 4) to yield the desired product (2.0 mg, 1% yield).

LC-MS (method 10): Rt=2.21 min; MS (ESIpos): m/z=396 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.94), 0.008(1.33), 1.848 (13.09), 2.221 (13.78), 2.327 (0.49), 2.670 (0.64), 3.688(16.00), 7.357 (2.02), 7.379 (4.89), 7.385 (1.96), 7.396 (1.47), 7.402(2.85), 7.509 (2.54), 7.514 (1.09), 7.523 (2.78), 7.531 (2.23), 7.539(0.87), 7.545 (1.91), 8.456 (2.78), 9.455 (2.52).

Example 2684-[1-(cyclopropylmethyl)-5-{[6-(4-fluoro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-4-methyl-1H-pyrazol-3-yl]benzonitrile

A microwave vial was charged with4-[5-amino-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(300 mg, 1.19 mmol),4-chloro-6-(4-fluoro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (296 mg,1.31 mmol) and sodium phenolate (152 mg, 1.31 mmol) and the contentswere suspended in 1,4-dioxane (3.4 mL). The reaction mixture wasdegassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (14.2mg, 15.5 μmol) and XantPhos (20.6 mg, 35.7 μmol) were added and thereaction mixture was degassed again for 1 min. The vial was sealed andheated at 85° C. overnight while vigorously shaking. After cooling toambient temperature, the reaction mixture was filtered and concentrated.The residue was redissolved in dimethylsulfoxide and purified bypreparative HPLC (method 4) to yield the desired product (54 mg, 10%yield).

LC-MS (method 11): R_(t)=1.54 min; MS (ESIpos): m/z=443 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.70), 0.008(0.69), 0.302 (2.50), 0.314 (2.76), 0.431 (2.58), 0.451 (2.76), 1.174(0.36), 1.186 (0.69), 1.193 (0.66), 1.205 (1.03), 1.217 (0.63), 1.223(0.66), 1.236 (0.34), 2.060 (16.00), 2.209 (2.74), 2.329 (0.19), 2.671(0.21), 3.859 (2.43), 3.876 (2.39), 7.885 (0.90), 7.907 (10.87), 7.933(0.90), 8.473 (0.52), 9.478 (0.62).

Example 269N-[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(4-fluoro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged with4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (79.2 mg, 361μmol), 4-chloro-6-(4-fluoro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine(90.0 mg, 397 μmol) and sodium phenolate (46.1 mg, 397 μmol) and thecontents were suspended in 1,4-dioxane (1.0 mL). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium(4.30 mg, 4.69 μmol) and XantPhos (6.27 mg, 10.8 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously shaking. After coolingto ambient temperature, the reaction mixture was filtered andconcentrated. The residue was redissolved in dimethylsulfoxide andpurified by preparative HPLC (XBridge C18 5 μm 100×30 mm, solvent A:water, solvent B: acetonitrile, flow: 65 mL/min plus 5 mL 2% formic acidin water, gradient 0-2 min: 50% B, 2-2.2 min: to 70% B, 2.2-7 min: 70 to92% B, 7-9 min: 92% B) to yield the desired product (4 mg, 3% yield).

LC-MS (method 10): R_(t)=2.33 min; MS (ESIpos): m/z=410 [M+H]⁺

Example 2706-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]-N-[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]pyrimidin-4-amine

A solution of4-chloro-6-[4-chloro-5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine(170 mg, 609 μmol) and4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (147 mg, 670μmol) in 1-methoxy-2-propanol (3.4 ml, 35 mmol) was treated withconcentrated hydrochloric acid (150 μl, 12 M, 1.8 mmol) and stirredovernight at 120° C. The mixture was purified by preparative HPLC(method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent:A=water (0.01% formic acid), B=acetonitrile/gradient: 0.00-5.00 min=10%B, 6.50 min=20% B, 17.0-19.75 min=100% B, 19.75-23.00 min=90% B) toyield 90.2 mg of the desired product (32%).

LC-MS (method 11): R_(t)=1.59 min; MS (ESIpos): m/z=462 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.869 (3.71), 0.888(7.95), 0.907 (3.64), 1.074 (0.65), 1.091 (1.29), 1.109 (0.64), 2.283(14.46), 2.310 (2.49), 2.329 (2.42), 2.347 (0.78), 3.375 (0.65), 3.393(0.62), 3.659 (16.00), 7.360 (2.09), 7.382 (4.58), 7.405 (3.18), 7.504(2.72), 7.518 (3.05), 7.525 (2.43), 7.539 (1.91), 7.905 (1.24), 8.037(2.61), 8.168 (1.13), 8.501 (3.10), 9.654 (1.27).

Example 2716-[3,5-dimethyl-4-(5-methyl-1,3,4-oxadiazol-2-yl)-1H-pyrazol-1-yl]-N-[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]pyrimidin-4-amine

A solution ofN′-acetyl-1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbohydrazide(56.8 mg, 116 μmol) in tetrahydrofuran (2.5 ml, 31 mmol) was treatedwith Burgess Reagent (38.6 mg, 162 μmol) and stirred overnight atambient temperature. The mixture was purified using preparative HPLC(method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent:A=water (0.01% formic acid), B=acetonitrile/gradient: 0.00-5.00 min=10%B, 6.50 min=20% B, 17.0-19.75 min=100% B, 19.75-23.00 min=90% B). Toremove remaining trimethylamine the product after preparative HPLC wasresolved in dichloromethane, extracted with water, washed with saturatedammonium chloride solution, water, dried over Extrelut NT3 andconcentrated to yield 30.4 mg (56%) of the desired product.

LC-MS (method 10): R_(t)=1.96 min; MS (ESIpos): m/z=474 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.879 (3.68), 0.898(7.78), 0.916 (3.67), 1.091 (0.72), 1.974 (1.96), 2.299 (1.24), 2.317(2.74), 2.336 (2.65), 2.355 (0.93), 2.366 (0.47), 2.460 (15.47), 2.573(16.00), 2.957 (15.09), 3.375 (0.41), 3.656 (15.14), 3.786 (0.58), 3.803(0.56), 4.905 (0.66), 7.186 (0.52), 7.361 (2.02), 7.383 (4.36), 7.405(2.66), 7.440 (1.54), 7.505 (2.68), 7.519 (3.07), 7.526 (2.50), 7.540(1.94), 8.537 (2.85), 9.548 (1.83).

Example 272[1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl][3-(trifluoromethyl)pyrrolidin-1-yl]methanone

A solution of [A9 and 3-(trifluoromethyl)pyrrolidine (31.9 mg, 230 μmol)in N,N-diisopropylethylamine (60 μl, 340 μmol) was tretaed with HATU(65.5 mg, 172 μmol) and dimethylformamide (1.0 ml, 13 mmol) and stirredovernight at ambient temperature. The mixture was purified bypreparative HPLC ((method: column: Reprosil C18; 10 μm; 125×30 mm/flow:50 mL/min/solvent: A=water (0.01% formic acid), B=acetonitrile/gradient:0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75 min=100% B, 19.75-23.00min=90% B) to yield 54.1 (85%) of the desired product.

LC-MS (method 10): R_(t)=2.01 min; MS (ESIpos): m/z=557 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.75), 0.008(0.47), 0.874 (3.50), 0.893 (7.71), 0.911 (3.47), 1.074 (1.72), 1.092(3.48), 1.109 (1.73), 2.017 (0.44), 2.179 (13.70), 2.289 (0.89), 2.308(2.35), 2.327 (2.29), 2.345 (0.73), 2.604 (12.81), 3.358 (1.11), 3.376(2.42), 3.393 (2.45), 3.410 (1.05), 3.654 (16.00), 7.359 (2.21), 7.365(1.09), 7.381 (6.03), 7.399 (1.06), 7.404 (2.68), 7.502 (2.64), 7.507(1.22), 7.515 (2.93), 7.523 (2.22), 7.532 (0.93), 7.537 (1.85), 8.481(3.24), 9.441 (2.10).

Example 2731-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3-methyl-5,6-dihydrocyclopenta[c]pyrazol-4(1H)-one

Under an argon atmosphere, a round-bottom flask was charged with4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (228 mg, 1.04mmol),1-(6-chloropyrimidin-4-yl)-3-methyl-5,6-dihydrocyclopenta[c]pyrazol-4(1H)-one(284 mg, 1.14 mmol) and sodium phenolate (181 mg, 1.56 mmol) and thecontents were suspended in 1,4-dioxane (3.0 mL). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium(18.0 mg, 31.1 μmol) and XantPhos (14.3 mg, 15.6 μmol) were added andthe reaction mixture was degassed again for 1 min. The reaction mixturewas heated at 85° C. overnight while vigorously stirring. After coolingto ambient temperature, the reaction mixture was filtered andconcentrated. The residue was redissolved in dimethylsulfoxide andpurified by preparative HPLC (column: Chromatorex C18; 250*30 mm, 10 μM,flow 10 to 50 mL/min, isocratic acetonitrile/water (containing 0.1%trifluoroacetic aicd) 20/80 as some component precipitated on thecolumn; then flow 75 mL/min gradient acetonitrile/water (containing 0.1%trifluoroacetic acid) 25/75 to 95/5) to yield the desired product (61mg, 13% yield) along with the regioisomer2-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3-methyl-5,6-dihydrocyclopenta[c]pyrazol-4(2H)-one(see below).

LC-MS (method 9): R_(t)=1.02 min; MS (ESIpos): m/z=432 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.50), −0.008(4.33), 0.008 (4.09), 0.146 (0.51), 0.869 (3.60), 0.888 (8.15), 0.907(3.72), 2.289 (0.95), 2.312 (16.00), 2.326 (3.03), 2.345 (0.83), 2.367(0.51), 2.523 (1.71), 2.670 (0.59), 2.711 (0.46), 2.804 (0.87), 2.934(2.08), 2.940 (2.04), 2.947 (2.35), 2.953 (2.20), 2.959 (2.23), 3.347(2.89), 3.353 (2.98), 3.360 (3.46), 3.365 (3.55), 3.372 (4.03), 3.666(15.57), 7.362 (2.92), 7.384 (4.99), 7.406 (2.89), 7.507 (2.71), 7.512(1.26), 7.521 (3.05), 7.529 (2.50), 7.543 (2.07), 8.503 (2.79), 9.560(1.63).

Example 2742-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3-methyl-5,6-dihydrocyclopenta[c]pyrazol-4(2H)-one

This compound was obtained as a by-product during the synthesis of theregioisomer1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3-methyl-5,6-dihydrocyclopenta[c]pyrazol-4(1H)-one(see above). Preparative HPLC purification yielded the title compound(6.0 mg, 81% purity, 1% yield).

LC-MS (method 9): R_(t)=1.00 min; MS (ESIpos): m/z=432 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.150 (1.70), 0.146(1.74), 0.874 (3.91), 0.893 (8.37), 0.911 (4.15), 1.236 (0.48), 1.848(5.75), 2.313 (4.60), 2.332 (4.63), 2.366 (2.25), 2.383 (2.76), 2.669(2.49), 2.710 (1.77), 2.804 (15.52), 2.902 (3.54), 2.934 (3.68), 3.657(16.00), 3.743 (0.71), 7.163 (1.12), 7.243 (3.91), 7.359 (5.04), 7.382(7.69), 7.404 (6.09), 7.433 (4.73), 7.506 (3.30), 7.520 (3.78), 7.542(2.59), 7.980 (1.67), 8.000 (1.53), 8.539 (3.47), 9.593 (2.21).

Example 2756-(3,5-dimethyl-1H-pyrazol-1-yl)-N-[5-(4-fluorophenyl)-1-methyl-4-{[3-(trifluoromethyl)azetidin-1-yl]methyl}-1H-pyrazol-3-yl]pyrimidin-4-amine

Under an argon atmosphere,3-{[6-(3,5-dimethyl-1H-pyrazol-1-yl]amino}-5-(4-fluorophenyl)-1-methyl-1H-pyrazole-4-carbaldehyde(50.0 mg, 128 μmol) and 3-(trifluoromethyl)azetidine (19.2 mg, 153 μmol)were dissolved in tetrahydrofuran (2.0 mL) and acetic acid (22 μl, 380μmol) and sodium triacetoxyborohydride (32.5 mg, 153 μmol) were added.The reaction mixture was stirred overnight at ambient temperature. Waterwas carefully added to quench the reaction, which was then extractedwith ethyl acetate (3×). The combined organic phase extracts were driedover sodium sulfate and concentrated. The residue was purified bypreparative HPLC (XBridge C18 5 μm 100×30 mm, solvent A: water, solventB: acetonitrile, flow: 65 mL/min plus 5 mL 2% formic acid in water,gradient 0-2 min: 10% B, 2-2.2 min: to 30% B, 2.2-7 min: 30 to 70% B,7-7.5 min: to 92% B, 7.5-9 min: 92% B) to yield the desired product (3.0mg, 5% yield)

LC-MS (method 9): R_(t)=0.78 min; MS (ESIpos): m/z=501 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.83), 0.008(1.83), 2.199 (15.19), 2.632 (13.00), 3.044 (2.43), 3.256 (3.04), 3.266(2.59), 3.392 (5.94), 3.683 (16.00), 6.147 (3.68), 7.370 (2.01), 7.392(4.40), 7.414 (2.52), 7.566 (2.42), 7.580 (2.74), 7.588 (2.37), 7.596(0.95), 7.602 (2.00), 7.773 (1.19), 8.486 (3.60), 9.320 (3.64).

Example 2762-[1-(6-{[4-chloro-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]propan-2-ol

Under an argon atmosphere, ethyl1-(6-{[4-chloro-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(95.0 mg, 202 μmol) was dissolved in tetrahydrofuran (4.0 mL) and thesolution cooled to 0° C. A solution of bromo(methyl)magnesium (1.0 ml,1.0 M, 1 0 mmol) was added dropwise and the reaction mixture was stirredovernight at ambient temperature. The reaction mixture was carefullyquenched by addition of aqueous Na₂EDTA solution (10%) and ethyl acetatewas added. After standing overnight, the organic phase was decanted andconcentrated. The residue was purified by flash column chromatography(SNAP Ultra 25 g, cyclohexane/ethyl acetate gradient 95/5 to 5/95) toyield the desired product (22 mg, 24% yield).

LC-MS (method 10): R_(t)=1.87 min; MS (ESIpos): m/z=456 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.68), 0.008(0.81), 1.157 (0.35), 1.175 (0.73), 1.193 (0.38), 1.237 (0.17), 1.472(16.00), 1.988 (1.30), 2.282 (8.01), 2.328 (0.21), 2.670 (0.22), 2.727(8.28), 2.751 (0.63), 3.724 (0.51), 3.763 (8.50), 4.021 (0.32), 4.038(0.32), 4.851 (3.08), 4.872 (0.23), 5.754 (0.56), 7.211 (2.18), 7.321(0.16), 7.407 (1.05), 7.429 (2.33), 7.451 (1.33), 7.623 (1.28), 7.629(0.60), 7.637 (1.38), 7.645 (1.26), 7.654 (0.50), 7.659 (1.07), 8.474(1.86), 9.529 (1.77).

Example 2772-[1-(6-{[4-chloro-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]pronan-2-ol

Under an argon atmosphere, ethyl1-(6-{[4-chloro-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(180 mg, 383 μmol) was dissolved in tetrahydrofuran (7.6 mL) and thesolution cooled to 0° C. A solution of bromo(methyl)magnesium (1.9 mL,1.0 M, 1.9 mmol) was added dropwise and the reaction mixture was stirredovernight at ambient temperature. The reaction mixture was carefullyquenched by addition of aqueous Na₂EDTA solution (10%) and ethyl acetatewas added. After standing overnight, the organic phase was decanted andconcentrated. The residue was purified by flash column chromatography(SNAP Ultra 25 g, cyclohexane/ethyl acetate gradient 95/5 to 5/95) toyield the desired product (100 mg, 57% yield).

LC-MS (method 10): R_(t)=1.88 min; MS (ESIpos): m/z=456 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.48 (s, 6H), 2.29 (s,3H), 2.75 (s, 3H), 3.73 (s, 3H), 4.87 (s, 1H), 6.92-7.22 (br s, 1H),7.26-7.36 (m, 2H), 7.81-7.96 (m, 2H), 8.50 (s, 1H), 9.69 (s, 1H).

Example 2782-[4-chloro-1-(6-{[4-chloro-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3-methyl-1H-pyrazol-5-yl]propan-2-ol

Under an argon atmosphere, ethyl4-chloro-1-(6-{[4-chloro-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate(154 mg, 314 μmol) was dissolved in tetrahydrofuran (6.2 mL) and thesolution cooled to 0° C. A solution of bromo(methyl)magnesium (1.6 mL,1.0 M, 1.6 mmol) was added dropwise and the reaction mixture was stirredovernight at ambient temperature. The reaction mixture was carefullyquenched by addition of aqueous Na₂EDTA solution (10%) and ethyl acetatewas added. After standing overnight, the organic phase was decanted andconcentrated. The residue was purified by flash column chromatography(SNAP Ultra 25 g, cyclohexane/ethyl acetate gradient 95/5 to 5/95) toyield the desired product (110 mg, 70% yield).

LC-MS (method 10): R_(t)=2.24 min; MS (ESIpos): m/z=476 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.40), 0.008(0.50), 1.157 (1.76), 1.175 (3.58), 1.184 (0.46), 1.193 (1.83), 1.398(0.34), 1.541 (1.85), 1.601 (1.36), 1.614 (16.00), 1.989 (6.48), 2.196(5.94), 2.650 (1.61), 2.674 (0.19), 3.725 (1.58), 3.737 (9.23), 3.763(0.68), 4.003 (0.51), 4.021 (1.55), 4.039 (1.53), 4.057 (0.52), 5.139(0.42), 6.612 (1.56), 7.300 (1.73), 7.305 (0.67), 7.322 (3.57), 7.340(0.68), 7.345 (1.90), 7.429 (0.19), 7.862 (0.28), 7.867 (0.30), 7.874(1.77), 7.879 (0.90), 7.888 (1.88), 7.896 (1.91), 7.904 (0.74), 7.910(1.57), 8.531 (0.27), 8.564 (0.17), 8.586 (1.34), 9.843 (0.27), 9.979(1.29).

Example 2792-[1-(6-{[4-chloro-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3-methyl-1H-pyrazol-5-yl]propan-2-ol

Under an argon atmosphere, ethyl1-(6-{[4-chloro-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate(124 mg, 272 μmol) was dissolved in tetrahydrofuran (5.4 mL) and thesolution cooled to 0° C. A solution of bromo(methyl)magnesium (1.4 mL,1.0 M, 1.4 mmol) was added dropwise and the reaction mixture was stirredovernight at ambient temperature. The reaction mixture was carefullyquenched by addition of aqueous Na₂EDTA solution (10%) and ethyl acetatewas added. After standing overnight, the organic phase was decanted andconcentrated. The residue was purified by flash column chromatography(SNAP Ultra 25 g, cyclohexane/ethyl acetate gradient 95/5 to 5/95) toyield the desired product (80 mg, 63% yield).

LC-MS (method 10): R_(t)=2.01 min; MS (ESIpos): m/z=442 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.74), 0.008(0.75), 1.450 (2.00), 1.483 (16.00), 2.213 (10.55), 2.647 (0.80), 2.670(0.18), 3.744 (0.22), 3.756 (1.07), 3.778 (11.86), 5.022 (0.34), 5.754(0.73), 6.297 (4.03), 6.311 (0.29), 7.357 (2.77), 7.411 (1.70), 7.434(3.33), 7.451 (0.81), 7.456 (1.85), 7.614 (0.17), 7.633 (1.90), 7.647(2.07), 7.656 (2.18), 7.661 (3.94), 7.669 (1.69), 8.476 (0.22), 8.568(2.66), 9.569 (0.20), 9.844 (1.73).

Example 280(±)-1-[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]propan-1-ol(racemic)

Under an argon atmosphere a Schlenk tube was charged with titaniumisopropoxide (300 μl, 1.0 mmol) in tetrahydrofuran (2.0 ml, 25 mmol). At−18° C. ethylmagensium bromide 1.0 M solution in tetrahydrofuran (3.1ml, 1.0 M, 3.1 mmol) was added. The mixture was stirred 30 minutes at−18° C., subsequently a solution of ethyl1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(250 mg, 100% purity, 511 μmol) in 1.5 mL tetrahydrofuran was added andthe resulting mixture was stirred at ambient temperature overnight. Themixture was diluted with saturated aqueous ammonium chloride solutionand water and extracted with ethyl acetate (3×). The combined organicphases were washed with water, brine, dried over sodium sulfate andconcentrated under reduced pressure. The crude product was purified bypreparative HPLC (method: column: Reprosil C18; 10 μm; 125×30 mm/flow:50 mL/min/solvent: A=water (0.01% formic acid), B=acetonitrile/gradient:0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75 min=100% B,19.75-23.00min=90% B) and subsequent flash-chromatography on silica gelto yield 41.5 mg (16%) of the described product along with1-[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]cyclopropanol(41.5 mg, 18%).

LC-MS (method 10): R_(t)=20.40 min; MS (ESIpos): m/z=476 [M+H]⁺

¹H-NMR (600 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.005 (0.75), 0.297(2.47), 0.304 (2.53), 0.428 (2.54), 0.441 (2.59), 0.793 (2.69), 0.806(5.60), 0.818 (2.82), 1.181 (0.43), 1.189 (0.77), 1.195 (0.76), 1.201(1.04), 1.209 (0.67), 1.213 (0.70), 1.222 (0.43), 1.227 (0.42), 1.234(0.56), 1.359 (1.53), 1.571 (0.54), 1.582 (0.64), 1.594 (0.64), 1.725(0.43), 1.737 (0.70), 1.748 (0.70), 1.759 (0.59), 2.009 (14.10), 2.185(0.48), 2.216 (2.02), 2.627 (16.00), 2.717 (0.79), 3.832 (2.06), 3.843(2.07), 4.475 (0.95), 4.480 (0.96), 4.917 (1.75), 4.921 (1.75), 7.255(2.00), 7.270 (4.10), 7.285 (2.22), 7.720 (1.39), 7.730 (1.92), 7.743(1.41), 8.454 (0.54), 9.331 (0.54).

Example 281 ethyl[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]acetate

A microwave vial was charged ethyl[1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]acetate (1.09g, 3.71 mmol) and1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine(1.20 g, 83% purity, 4.08 mmol) and the contents were suspended in1,4-dioxane (15 ml, 180 mmol). The reaction mixture was degassed with Arfor 3 min. Tris(dibenzylidenaceton)dipalladium (102 mg, 111 μmol) andXantphos (129 mg, 222 μmol) were added and the reaction mixture wasdegassed again for 1 min and heated to 85° C. At this temperature andsodium phenolate (473 mg, 4.08 mmol) was added. The vial was sealed andheated at 85° C. for 90 minutes while vigorously stirring. After coolingto ambient temperature, the reaction mixture was diluted with brine andextracted with ethyl acetate (2×). The combined organic phases weredried over sodium sulfate and concentrated under reduced pressure. Thecrude product was purified by flash-chromatography on silic gel (column:Biotage SNAP Ultra 25 g, solvent: 92% dichloromethane/8% ethyl acetateto 66% ethyl acetate) to yield the desired product (1.13 g, 61%).

LC-MS (method 10): R_(t)=2.29 min; MS (ESIpos): m/z=504 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.295 (2.56), 0.307(2.83), 0.424 (2.65), 0.444 (2.84), 1.166 (4.39), 1.183 (9.03), 1.201(5.12), 1.218 (0.78), 1.230 (0.40), 1.980 (0.74), 2.012 (14.68), 2.134(3.16), 2.582 (16.00), 3.321 (14.65), 3.832 (2.44), 3.849 (2.39), 4.049(1.29), 4.067 (3.84), 4.085 (3.80), 4.102 (1.25), 7.252 (2.15), 7.274(4.33), 7.296 (2.38), 7.719 (1.60), 7.733 (2.08), 7.739 (2.01), 7.754(1.46), 8.470 (0.65), 9.379 (0.74).

Example 282[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]methanol

Under an argon atmosphere a solution of ethyl1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(160 mg, 327 μmol) in (3.0 ml, 37 mmol) was treated with lithiumaluminium hydride (330 μl, 1.0 M in tetrahydrofuran, 330 μmol) at −78°C. The resulting mixture was stirred for 30 minutes at this temperatureand subsequently 30 minutes at ambient temperature. The mixture wasdiluted with methanol and purified by preparative HPLC (method: column:Reprosil C18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent: A=water (0.01%formic acid), B=acetonitrile/gradient: 0.00-5.00 min=10% B, 6.50 min=20%B, 17.0-19.75 min=100% B, 19.75-23.00 min=90% B) to yield 41.0 mg (25%)of the desired product.

LC-MS (method 10): R_(t)=1.78 min; MS (ESIpos): m/z=448 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.66), 0.008(1.38), 0.292 (2.17), 0.303 (2.34), 0.420 (2.22), 0.440 (2.29), 0.868(0.52), 0.887 (1.26), 0.906 (0.54), 1.157 (0.46), 1.175 (0.73), 1.183(0.64), 1.195 (0.96), 1.207 (0.60), 1.213 (0.56), 1.986 (0.50), 2.006(13.72), 2.132 (0.55), 2.196 (2.89), 2.207 (3.77), 2.318 (0.52), 2.328(0.82), 2.612 (3.29), 2.620 (16.00), 2.661 (0.59), 2.670 (0.47), 3.650(2.55), 3.826 (2.22), 3.843 (2.17), 4.288 (2.85), 4.301 (3.07), 4.693(0.98), 4.706 (1.87), 4.720 (0.85), 7.251 (2.01), 7.274 (4.19), 7.296(2.29), 7.323 (0.47), 7.379 (0.74), 7.401 (0.46), 7.500 (0.42), 7.514(0.46), 7.714 (1.39), 7.728 (1.82), 7.749 (1.31), 8.444 (0.69), 8.465(0.64), 9.317 (0.45), 9.361 (0.66).

Example 283(±)-1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,4-dimethyl-1,4,5,6-tetrahydrocyclopenta[c]pyrazol-4-ol(racemate)

Under an argon atmosphere,1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3-methyl-5,6-dihydrocyclopenta[c]pyrazol-4(1H)-one(298 mg, 56% purity, 365 μmol) was dissolved in tetrahydrofuran (3.4 mL)and the solution chilled with a water bath. A solution ofbromo(methyl)magnesium (2.6 mL, 1.0 M, 2.6 mmol) was added dropwise andthe reaction mixture was stirred for 30 min at ambient temperature. Aseond aliquot of bromo(methyl)magnesium (1.0 mL, 1.0 M, 1.0 mmol) wasadded and the reaction mixture was stirred at ambient temperatureovernight. A third aliquot of bromo(methyl)magnesium (1.0 mL, 1.0 M, 1.0mmol) was added and the reaction mixture was stirred at ambienttemperature for 1 h. The reaction mixture was carefully quenched byaddition of aqueous Na₂EDTA (10%) and extracted with ethyl acetate (2×).The combined organic phase extracts were dried over magnesium sulfateand concentrated. The residue was purified by flash columnchromatography (SNAP Ultra 10 g, cyclohexane/ethyl acetate gradient88/12 to 0/100) to yieldan impure product fraction. The residue wasresuspended in acetonitrile/water and the insoluble solids were removedby filtration. The filtrate was purified by preparative HPLC (column:Chromatorex C18; 250*30 mm, 10 μM, flow 75 mL/min, gradientacetonitrile/water 5/95 to 95/5) to yield the desired product (12.0 mg,7% yield).

LC-MS (method 10): R_(t)=1.97 min; MS (ESIpos): m/z=474 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.48), −0.022(0.48), −0.008 (4.07), 0.008 (3.85), 0.146 (0.49), 0.281 (2.50), 0.292(2.69), 0.414 (2.66), 0.433 (2.83), 1.171 (0.77), 1.183 (1.12), 1.201(0.73), 1.213 (0.42), 1.234 (0.79), 1.446 (8.03), 1.470 (1.87), 2.003(16.00), 2.192 (2.51), 2.304 (0.42), 2.327 (0.64), 2.366 (0.35), 2.431(0.94), 2.444 (0.90), 2.453 (1.31), 2.469 (1.27), 2.475 (1.12), 2.654(3.28), 2.665 (0.60), 2.670 (0.67), 2.674 (0.53), 2.710 (0.45), 2.950(0.41), 2.962 (0.44), 2.970 (0.54), 2.982 (0.48), 2.992 (0.84), 3.005(0.82), 3.013 (0.81), 3.025 (0.58), 3.092 (0.62), 3.107 (0.84), 3.112(0.82), 3.126 (0.72), 3.135 (0.51), 3.149 (0.55), 3.169 (0.32), 3.825(2.41), 3.842 (2.38), 4.957 (2.74), 5.028 (0.53), 7.254 (1.91), 7.276(3.95), 7.298 (2.18), 7.721 (1.43), 7.735 (1.98), 7.754 (1.40), 8.424(0.48), 9.375 (0.54).

Example 284 ethyl1-[6-({1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3,5-dimethyl-1H-pyrazole-4-carboxylate

A microwave vial was charged with ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (258mg, 917 μmol),1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-5-amine(314 mg, 1.01 mmol) and sodium phenolate (117 mg, 1.01 mmol) and thecontents were suspended in 1,4-dioxane (2.2 mL). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium(109 mg, 119 μmol) and XantPhos (159 mg, 275 μmol) were added and thereaction mixture was degassed again for 1 min. The vial was sealed andheated at 90° C. overnight while vigorously shaking. After cooling toambient temperature, the reaction mixture was loaded on silica gel andpurified by flash column chromatography (SNAP Ultra 25 g,cyclohexane/ethyl acetate gradient 95/5 to 20/80) to yield the desiredproduct (210 mg, 40% yield).

LC-MS (method 10): R_(t)=2.58 min; MS (ESIpos): m/z=556 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.300 (2.94), 0.312(3.24), 0.346 (0.36), 0.359 (0.36), 0.430 (3.09), 0.450 (3.28), 1.172(0.47), 1.184 (0.85), 1.191 (0.83), 1.203 (1.23), 1.214 (0.82), 1.222(0.86), 1.234 (0.65), 1.287 (3.77), 1.305 (7.56), 1.323 (3.91), 1.398(1.27), 1.428 (0.16), 2.000 (1.51), 2.034 (16.00), 2.130 (0.31), 2.372(2.43), 2.473 (0.27), 2.671 (0.25), 2.712 (0.16), 2.912 (13.35), 2.952(0.19), 3.802 (0.44), 3.820 (0.54), 3.846 (2.54), 3.863 (2.49), 4.228(1.18), 4.246 (3.44), 4.264 (3.44), 4.282 (1.20), 4.949 (0.44), 7.342(0.34), 7.363 (0.34), 7.428 (3.51), 7.449 (3.89), 7.685 (0.41), 7.707(0.37), 7.816 (3.06), 7.837 (2.77), 8.539 (0.44), 9.555 (0.41).

Example 285 ethyl1-[6-({1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethyl)phenyl]-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3,5-dimethyl-1H-pyrazole-4-carboxylate

A microwave vial was charged with ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (163mg, 582 μmol),1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethyl)phenyl]-1H-pyrazol-5-amine(210 mg, 90% purity, 640 μmol) and sodium phenolate (74.3 mg, 640 μmol)and the contents were suspended in 1,4-dioxane (1.4 mL). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (69.3 mg, 75.6 μmol) and XantPhos(101 mg, 175 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 90° C. overnightwhile vigorously shaking. After cooling to ambient temperature, thereaction mixture was loaded on silica gel and purified by flash columnchromatography (SNAP Ultra 25 g, cyclohexane/ethyl acetate gradient 95/5to 20/80) to yield the desired product (70 mg, 21% yield).

LC-MS (method 10): R_(t)=2.56 min; MS (ESIpos): m/z=540 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.311 (2.85), 0.322(3.14), 0.356 (0.42), 0.372 (0.42), 0.438 (3.05), 0.458 (3.22), 1.186(0.57), 1.216 (1.32), 1.236 (1.25), 1.289 (3.81), 1.306 (7.52), 1.324(3.86), 1.398 (8.76), 2.035 (2.12), 2.066 (16.00), 2.329 (0.72), 2.376(2.44), 2.914 (13.27), 3.568 (0.41), 3.825 (0.59), 3.842 (0.68), 3.868(2.46), 3.885 (2.44), 4.230 (1.19), 4.248 (3.44), 4.265 (3.42), 4.283(1.19), 4.997 (0.64), 7.725 (0.54), 7.792 (3.62), 7.812 (4.92), 7.930(3.43), 7.950 (2.61), 8.544 (0.52), 9.577 (0.42).

Example 2864-[1-(cyclopropylmethyl)-4-methyl-5-({6-[5-methyl-3-(propan-2-yl)-1H-pyrazol-1-yl]pyrimidin-4-yl}amino)-1H-pyrazol-3-yl]benzonitrile

A microwave vial was charged with4-chloro-6-[5-methyl-3-(propan-2-yl)-1H-pyrazol-1-yl]pyrimidine (105 mg,90% purity, 399 μmol),4-[5-amino-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(130 mg, 85% purity, 439 μmol) and sodium phenolate (51.0 mg, 439 μmol)and the contents were suspended in 1,4-dioxane (0.96 mL). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (4.75 mg, 5.19 μmol) and XantPhos(6.93 mg, 12.0 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 90° C. overnightwhile vigorously shaking. After cooling to ambient temperature, thereaction mixture was loaded on silica gel and purified by flash columnchromatography (SNAP Ultra 25 g, cyclohexane/ethyl acetate gradient 95/5to 20/80) to yield the desired product (52 mg, 28% yield).

LC-MS (method 10): R_(t)=2.44 min; MS (ESIpos): m/z=453 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.310 (2.39), 0.322(2.68), 0.436 (2.18), 0.455 (2.32), 1.200 (4.79), 1.214 (4.91), 1.398(5.34), 1.436 (0.25), 1.868 (0.18), 2.060 (11.40), 2.257 (0.18), 2.329(0.21), 2.350 (0.21), 2.640 (11.66), 2.671 (0.31), 2.888 (0.50), 3.569(0.42), 3.861 (2.16), 3.878 (2.14), 6.225 (3.00), 7.903 (16.00), 8.450(0.81), 9.430 (1.00).

Example 2871-{[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]methyl}cyclopropanol

Under an argon atmosphere a Schlenk tube was charged with titaniumisopropoxide (290 μl, 990 μmol) in tetrahydrofuran (1.9 ml, 24 mmol) at−18° C. At this temperature ethylmagnesium bromide (3.0 ml, 1.0 M intetrahydrofuran, 3.0 mmol) was added at the mixture was stirred 30minutes at −18° C. Subsequently a solution of ethyl[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]acetate(250 mg, 496 μmol) in 1.5 mL tetrahydrofuran was added and it wasstirred 20 minutes at −18° C. and overnight at ambient temperature. Themixture was diluted with potassium sodium tartrate solution and water.The mixture was extracted with ethyl acetate (3×). The combined organicphases were washed with water, brine, dried over sodium sulfate andconcentrated under reduced pressure. The crude product was purified bypreparative HPLC (method: column: Reprosil C18; 10 μm; 125×30 mm/flow:50 mL/min/solvent: A=water (0.01% formic acid), B=acetonitrile/gradient:0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75 min=100% B, 19.75-23.00min=90% B) to yield 25.-9 mg (11%) of the desired product.

LC-MS (method 10): R_(t)=2.02 min; MS (ESIpos): m/z=488 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.008 (2.18), 0.290(2.81), 0.302 (3.04), 0.329 (1.30), 0.345 (3.97), 0.357 (1.56), 0.421(2.73), 0.441 (2.90), 0.498 (1.48), 0.510 (3.88), 0.525 (1.08), 1.073(0.49), 1.091 (0.95), 1.108 (0.47), 1.163 (0.42), 1.175 (0.75), 1.181(0.74), 1.194 (1.09), 1.206 (0.69), 1.212 (0.73), 1.968 (0.55), 2.006(15.61), 2.170 (3.39), 2.571 (1.00), 2.589 (16.00), 2.649 (4.73), 3.375(0.56), 3.392 (0.55), 3.825 (2.60), 3.842 (2.58), 5.213 (4.27), 7.251(2.28), 7.273 (4.82), 7.296 (2.71), 7.714 (1.73), 7.729 (2.30), 7.749(1.71), 8.451 (0.86), 9.331 (0.94).

Example 2881-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbonitrile

A microwave vial was charged1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbonitrile (1.00g, 77% purity, 3.30 mmol) and1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine(889 mg, 3.62 mmol) and the contents were suspended in 1,4-dioxane (15ml, 180 mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (90.5 mg, 98.9 μmol) and Xantphos(114 mg, 198 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (421 mg, 3.62 mmol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with saturatedsodium hydrogen carbonate solution and extracted with ethyl acetate(2×). The combined organic phases were washed with brine dried oversodium sulfate and concentrated under reduced pressure. The crudeproduct was purified by flash-chromatography on silica gel (column;Biotage Snap Ultra 50 g, solvent: dichloromethane/ethyl acetate 20:1) toyield the desired product (870 mg, 57%).

LC-MS (method 10): R_(t)=2.24 min; MS (ESIpos): m/z=443 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.288 (2.39), 0.299(2.56), 0.422 (2.66), 0.442 (2.80), 1.171 (0.70), 1.189 (1.03), 1.201(0.71), 1.208 (0.69), 1.975 (1.41), 2.005 (14.57), 2.329 (2.06), 2.796(16.00), 3.787 (0.44), 3.804 (0.58), 3.828 (2.01), 3.844 (1.99), 4.906(0.40), 7.252 (2.06), 7.275 (4.16), 7.297 (2.32), 7.713 (1.40), 7.729(1.91), 7.745 (1.31).

Example 2892-{1-[6-({1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3,5-dimethyl-1H-pyrazol-4-yl}propan-2-ol

Under an argon atmosphere, ethyl1-[6-({1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3,5-dimethyl-1H-pyrazole-4-carboxylate(150 mg, 270 μmol) was dissolved in tetrahydrofuran (5.3 mL) and thesolution cooled to 0° C. A solution of bromo(methyl)magnesium (1.3 ml,1.0 M, 1.3 mmol) was added dropwise and the reaction mixture was stirredovernight at ambient temperature. The reaction mixture was carefullyquenched by addition of aqueous Na₂EDTA solution (10%) and extractedwith ethyl acetate. The organic phase extract was concentrated and theresidue was purified by flash column chromatography (SNAP Ultra 25 g,cyclohexane/ethyl acetate gradient 95/5 to 5/95) to yield the desiredproduct (28 mg, 19% yield).

LC-MS (method 10): R_(t)=2.22 min; MS (ESIpos): m/z=542 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.50), 0.146(0.48), 0.296 (2.01), 0.308 (2.20), 0.426 (1.92), 0.446 (2.05), 1.199(0.82), 1.398 (0.45), 1.464 (16.00), 1.988 (0.67), 2.027 (11.59), 2.264(2.49), 2.327 (0.58), 2.367 (0.35), 2.670 (0.56), 2.711 (0.39), 2.742(11.85), 3.840 (1.95), 3.857 (1.90), 4.854 (3.35), 7.425 (2.49), 7.446(2.70), 7.812 (2.72), 7.834 (2.49), 8.464 (0.65), 9.379 (0.71).

Example 2902-{4-chloro-1-[6-({1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3-methyl-1H-pyrazol-5-yl}propan-2-ol

Under an argon atmosphere, ethyl4-chloro-1-[6-({1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3-methyl-1H-pyrazole-5-carboxylate(176 mg, 306 μmol) was dissolved in tetrahydrofuran (6.0 mL) and thesolution cooled to 0° C. A solution of bromo(methyl)magnesium (1.5 ml,1.0 M, 1.5 mmol) was added dropwise and the reaction mixture was stirredovernight at ambient temperature. The reaction mixture was carefullyquenched by addition of aqueous Na₂EDTA solution (10%) and extractedwith ethyl acetate. The organic phase extract was concentrated and theresidue was purified by flash column chromatography (SNAP Ultra 25 g,cyclohexane/ethyl acetate gradient 95/5 to 5/95) to yield the desiredproduct (42 mg, 23% yield).

LC-MS (method 10): R_(t)=2.58 min; MS (ESIpos): m/z=562 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.12), 0.008(1.16), 0.296 (2.44), 0.308 (2.69), 0.431 (2.56), 0.450 (2.72), 1.142(0.16), 1.158 (1.08), 1.176 (2.34), 1.184 (0.79), 1.194 (1.71), 1.207(0.77), 1.215 (0.79), 1.227 (0.49), 1.233 (0.47), 1.398 (11.86), 1.527(0.66), 1.601 (13.94), 1.989 (3.13), 2.001 (0.30), 2.023 (2.04), 2.036(16.00), 2.181 (2.07), 2.329 (0.22), 2.524 (0.72), 2.642 (1.54), 2.667(0.23), 2.711 (0.33), 3.853 (2.61), 3.870 (2.51), 4.004 (0.25), 4.021(0.78), 4.039 (0.77), 4.057 (0.25), 7.425 (3.75), 7.446 (4.06), 7.792(0.76), 7.810 (4.44), 7.832 (3.78), 8.552 (0.41), 9.682 (0.27).

Example 2912-{1-[6-({1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3-methyl-1H-pyrazol-5-yl}propan-2-ol

Under an argon atmosphere, ethyl1-[6-({1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3-methyl-1H-pyrazole-5-carboxylate(114 mg, 211 μmol) was dissolved in tetrahydrofuran (4.2 mL) and thesolution cooled to 0° C. A solution of bromo(methyl)magnesium (1.1 ml,1.0 M in tetrahydrofuran, 1.1 mmol) was added dropwise and the reactionmixture was stirred overnight at ambient temperature. The reactionmixture was carefully quenched by addition of aqueous Na₂EDTA solution(10%) and extracted with ethyl acetate. The organic phase extract wasconcentrated and the residue was purified by flash column chromatography(SNAP Ultra 25g, cyclohexane/ethyl acetate gradient 95/5 to 5/95) toyield the desired product (75 mg, 66% yield).

LC-MS (method 10): R_(t)=2.37 min; MS (ESIpos): m/z=528 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.31), 0.146(0.32), 0.300 (2.12), 0.311 (2.30), 0.428 (2.09), 0.448 (2.18), 1.157(0.97), 1.175 (2.10), 1.193 (1.49), 1.205 (0.88), 1.236 (0.41), 1.398(0.97), 1.489 (16.00), 1.988 (3.37), 2.043 (10.27), 2.202 (1.28), 2.328(0.41), 2.367 (0.34), 2.670 (0.40), 2.711 (0.35), 3.855 (1.73), 3.871(1.68), 4.003 (0.29), 4.021 (0.85), 4.039 (0.82), 4.056 (0.27), 6.300(1.52), 7.430 (2.63), 7.451 (2.85), 7.620 (2.69), 7.819 (1.77), 7.840(1.66), 8.545 (0.31), 9.644 (0.26).

Example 2922-{1-[6-({1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethyl)phenyl]-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3,5-dimethyl-1H-pyrazol-4-yl}propan-2-ol

Under an argon atmosphere, ethyl1-[6-({1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethyl)phenyl]-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3,5-dimethyl-1H-pyrazole-4-carboxylate(70.0 mg, 130 μmol) was dissolved in tetrahydrofuran (2.6 mL) and thesolution cooled to 0° C. A solution of bromo(methyl)magnesium (650 μl,1.0 M in tetrahydrofuran, 650 μmol) was added dropwise and the reactionmixture was stirred overnight at ambient temperature. The reactionmixture was carefully quenched by addition of aqueous Na₂EDTA solution(10%) and ethyl acetate was added. After standing overnight, the organicphase was decanted and concentrated. The residue was purified by flashcolumn chromatography (SNAP Ultra 25 g, cyclohexane/ethyl acetategradient 95/5 to 5/95) to yield the desired product (10 mg, 15% yield).

LC-MS (method 10): R_(t)=2.20 min; MS (ESIpos): m/z=526 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.41), −0.008(3.49), 0.008 (3.14), 0.146 (0.38), 0.307 (2.04), 0.319 (2.23), 0.436(1.92), 0.454 (2.05), 1.157 (0.50), 1.175 (1.12), 1.193 (0.95), 1.213(0.83), 1.232 (0.67), 1.398 (2.02), 1.466 (16.00), 1.988 (1.73), 2.060(11.72), 2.267 (2.43), 2.327 (0.50), 2.367 (0.33), 2.670 (0.45), 2.710(0.33), 2.745 (11.75), 3.862 (1.95), 3.879 (1.93), 4.021 (0.45), 4.038(0.43), 4.857 (3.33), 5.754 (0.41), 7.789 (2.50), 7.810 (3.42), 7.927(2.74), 7.947 (2.11), 8.465 (0.64), 9.405 (0.71).

Example 2932-{1-[6-({1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethyl)phenyl]-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3-methyl-1H-pyrazol-5-yl}propan-2-ol

Under an argon atmosphere, ethyl1-[6-({1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethyl)phenyl]-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3-methyl-1H-pyrazole-5-carboxylate(35.0 mg, 66.6 μmol) was dissolved in tetrahydrofuran (1.3 mL) and thesolution cooled to 0° C. A solution of bromo(methyl)magnesium (330 μl,1.0 M in tetrahydrofuran, 330 μmol) was added dropwise and the reactionmixture was stirred overnight at ambient temperature. The reactionmixture was carefully quenched by addition of aqueous Na₂EDTA solution(10%) and ethyl acetate was added. After standing overnight, the organicphase was decanted and concentrated. The residue was purified by flashcolumn chromatography (SNAP Ultra 25g, cyclohexane/ethyl acetategradient 95/5 to 5/95) to yield the desired product (17 mg, 49% yield).

LC-MS (method 10): R_(t)=2.34 min; MS (ESIpos): m/z=512 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.146 (0.17), 0.311(2.14), 0.322 (2.26), 0.437 (2.08), 0.457 (2.17), 1.158 (0.18), 1.175(0.37), 1.192 (0.43), 1.201 (0.65), 1.208 (0.65), 1.219 (0.97), 1.238(0.86), 1.398 (10.74), 1.492 (16.00), 1.989 (0.51), 2.076 (10.95), 2.209(1.32), 2.328 (0.25), 2.367 (0.18), 2.671 (0.26), 2.712 (0.18), 3.879(1.71), 3.894 (1.69), 6.303 (1.55), 7.616 (2.71), 7.794 (2.60), 7.815(3.44), 7.933 (2.07), 7.953 (1.65), 8.552 (0.32), 9.667 (0.28).

Example 2942-{4-chloro-1-[6-({1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethyl)phenyl]-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3-methyl-1H-pyrazol-5-yl}propan-2-ol

Under an argon atmosphere, ethyl4-chloro-1-[6-({1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethyl)phenyl]-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3-methyl-1H-pyrazole-5-carboxylate(45.0 mg, 80.4 μmol) was dissolved in tetrahydrofuran (1.6 mL) and thesolution cooled to 0° C. A solution of bromo(methyl)magnesium (400 μl,1.0 M in tetrahydrofuran, 400 μmol) was added dropwise and the reactionmixture was stirred overnight at ambient temperature. The reactionmixture was carefully quenched by addition of aqueous Na₂EDTA solution(10%) and ethyl acetate was added. After standing overnight, the organicphase was decanted and concentrated. The residue was purified by flashcolumn chromatography (SNAP Ultra 25 g, cyclohexane/ethyl acetategradient 95/5 to 5/95) to yield the desired product (22 mg, 44% yield).

LC-MS (method 10): R_(t)=2.56 min; MS (ESIpos): m/z=546 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.41), 0.146(0.44), 0.306 (2.81), 0.317 (3.03), 0.439 (2.87), 0.458 (2.98), 0.854(0.21), 1.141 (0.41), 1.157 (1.57), 1.175 (3.01), 1.193 (2.09), 1.208(1.32), 1.236 (1.25), 1.398 (6.01), 1.529 (0.84), 1.602 (16.00), 1.758(0.22), 1.905 (0.21), 1.988 (4.60), 2.055 (2.36), 2.067 (15.98), 2.183(2.64), 2.257 (0.53), 2.327 (0.51), 2.367 (0.46), 2.643 (1.56), 2.670(0.56), 2.711 (0.51), 3.875 (2.94), 3.892 (2.79), 4.003 (0.39), 4.021(1.13), 4.039 (1.16), 4.056 (0.43), 4.383 (0.17), 4.394 (0.17), 6.825(0.21), 7.790 (3.88), 7.811 (5.29), 7.924 (4.40), 7.944 (3.11), 8.556(0.48), 9.697 (0.34).

Example 2952-[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]-1,1,1,3,3,3-hexafluorobroban-2-ol

Molecular Sieves (4 Å) were placed in a round-bottom flask and dried ina vacuum drying-oven overnight at 120° C. After cooling to ambienttemperature, tetrabutylammonium fluoride trihydrate (197 mg, 705 μmol)was added and toluene (1.5 mL) was added and the suspension stirred for30 min. A solution of ethyl1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(115 mg, 235 μmol) in toluene (4.5 mL) was then added, the mixture wasstired for 5 min and cooled to 0° C. trimethyl(trifluoromethyl)silane(170 1.2 mmol) was then added and stirred at ambient temperature for 3h. Further aliquots of tetrabutylammonium fluoride trihydrate (98 mg,353 μmol) and trimethyl(trifluoromethyl)silane (85 μl, 0.6 mmol)dissolved in dry toluene (800 μL, dried over 4 Å molecular sieves) wereadded and the reaction mixture was stirred at ambient temperatureovernight. The reaction mixture was filtered through Celite and thefiltrate was concentrated. The residue was purified by flash columnchromatography (SNAP Ultra 25 g, cyclohexane/ethyl acetate gradient90/10 to 0/100) to yield the desired product (8 mg, 6% yield) along withimpure fractions. Impure fractions were concentrated and repurified byflash column chromatography and preparative HPLC (method 6) to yield thedesired product (18 mg, 13% yield).

LC-MS (method 11): Rt=1.54 min; MS (ESIpos): m/z=584 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.34), −0.008(2.74), 0.008 (3.12), 0.146 (0.32), 0.295 (2.70), 0.306 (3.00), 0.427(2.74), 0.446 (2.92), 1.168 (0.38), 1.180 (0.73), 1.187 (0.73), 1.199(1.12), 1.211 (0.69), 1.217 (0.72), 1.229 (0.37), 2.011 (16.00), 2.266(2.20), 2.323 (0.53), 2.328 (0.62), 2.367 (0.39), 2.670 (0.56), 2.711(0.63), 2.733 (9.33), 3.831 (2.38), 3.847 (2.35), 7.249 (2.57), 7.271(5.34), 7.294 (2.90), 7.709 (1.80), 7.724 (2.31), 7.731 (2.27), 7.745(1.72), 8.516 (3.86), 9.531 (0.39).

Example 296N-[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-{4-[(3-fluoroazetidin-1-yl)methyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-amine

A solution of1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbaldehyde (50.0 mg, 119 μmol) and 3-fluoroazetidine hydrochloride (1:1) (17.3mg, 155 μmol) in tetrahydrofuran (2.0 ml, 25 mmol) was treated withacetic acid (14 μl, 240 μmol). The mixture was stirred one hour atambient temperature, subsequently sodium triacetoxyborhydride (40.4 mg,191 μmol) was added and the mixture was again stirred overnight atambient temperature. Additional 1.6 equivalents sodiumtriacetoxyborhydride (40.4 mg, 0.19 mmol) were added and it was stirredan additional hour. The mixture was diluted with water and purified bypreparative HPLC (method: column: Reprosil C18; 10 μm; 125×30 mm/flow:50 mL/min/solvent: A=water (0.01% formic acid), B=acetonitrile/gradient:0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75 min=100% B, 19.75-23.00min=90% B) to yield 37.8 mg of the desired product (66%).

LC-MS (method 10): R_(t)=1.31 min; MS (ESIneg): m/z=477 [M−H]⁻

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.869 (3.77), 0.888(8.55), 0.906 (3.92), 1.856 (0.47), 2.194 (15.66), 2.249 (0.55), 2.281(0.95), 2.300 (2.81), 2.319 (2.74), 2.337 (0.95), 2.628 (16.00), 2.666(0.62), 3.022 (0.92), 3.033 (1.10), 3.039 (1.13), 3.045 (1.21), 3.057(1.17), 3.081 (1.04), 3.093 (1.17), 3.099 (1.16), 3.104 (1.23), 3.116(1.13), 3.316 (0.42), 3.450 (8.54), 3.465 (1.84), 3.469 (1.71), 3.473(1.76), 3.488 (2.16), 3.502 (1.52), 3.507 (1.44), 3.511 (1.40), 3.525(1.12), 3.604 (0.67), 5.032 (0.58), 5.045 (0.84), 5.058 (0.54), 5.177(0.56), 5.190 (0.83), 5.202 (0.55), 5.755 (3.32), 7.326 (3.03), 7.357(2.08), 7.379 (4.64), 7.401 (2.74), 7.498 (2.76), 7.503 (1.28), 7.512(3.11), 7.519 (2.43), 7.533 (2.01), 8.142 (5.42), 8.442 (4.14), 9.327(2.89).

Example 2976-{3,5-dimethyl-4-[(4-methylpiperazin-1-yl)methyl]-1H-pyrazol-1-yl}-N-[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]pyrimidin-4-amine

A solution of1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbaldehyde (50.0 mg, 119 μmol) and 1-methylpiperazine (17 μl, 150 μmol) intetrahydrofuran (2.0 ml, 25 mmol) was treated with acetic acid (14 μl,240 μmol) and stirred for one hour at room temperature. Subsequentlysodium triacetoxyborhydride (40.4 mg, 191 μmol) was added and it wasstirred again overnight at ambient temperature. The mixture was dilutedwith water and purified by preparative HPLC (method: column: ReprosilC18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent: A=water (0.01% formicacid), B=acetonitrile/gradient: 0.00-5.00 min=10% B, 6.50 min=20% B,17.0-19.75 min=100% B, 19.75-23.00 min=90% B) to yield 43.6 mg (73%) ofthe desired product.

LC-MS (method 10): R_(t)=1.32 min; MS (ESIneg): m/z=502 [M−H]⁻

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.869 (3.77), 0.888(8.64), 0.906 (3.95), 1.074 (0.71), 1.091 (1.47), 1.109 (0.74), 1.855(0.44), 2.147 (13.58), 2.177 (15.99), 2.233 (0.96), 2.281 (2.12), 2.299(4.20), 2.318 (4.37), 2.337 (2.75), 2.592 (16.00), 2.630 (0.52), 3.256(7.54), 3.283 (0.78), 3.357 (1.00), 3.375 (1.50), 3.392 (1.48), 3.410(0.97), 3.603 (0.68), 7.324 (3.04), 7.357 (2.10), 7.379 (4.74), 7.401(2.80), 7.498 (2.80), 7.503 (1.24), 7.511 (3.09), 7.519 (2.42), 7.528(0.96), 7.533 (2.02), 8.177 (1.89), 8.438 (4.02), 9.317 (2.98).

Example 2984-[5-({6-[4-(2-hydroxypropan-2-yl)-3,5-dimethyl-1H-pyrazol-1-yl]pyrimidin-4-yl}amino)-1,4-dimethyl-1H-pyrazol-3-yl]benzonitrile

A solution of ethyl1-(6-{[3-(4-cyanophenyl)-1,4-dimethyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(59.0 mg, 129 μmol) in tetrahydrofuran (2.0 ml, 25 mmol) was treated at0° C. with methylmagnesium bromide (150 μl, 3.0 M in diethyl ether, 450μmol) and stirred overnight at room temperature. The mixture was cooleddown to 0° C. and additional 3.5 equivalents of methylmagnesium bromide(150 μL, 3.0 M in diethyl ether, 459 μmol) were added. The mixture wasstirred 3 hours at ambient temperature. As no conversion could beobserved, a solution of methyl lithium (160 μl, 1.6 M in diethyl ether,260 μmol) was added at −18° C. and it was stirred overnight at ambienttemperature. Again no conversion was observed. The mixture was left overthe weekend and then a solution of methylmagnesium chloride (86 μl, 3.0M in tetrahydrofuran, 260 μmol) was added and again the mixture wasstirred overnight at room temperature. The mixture was diluted withmethanol and potassium sodium tartrate solution. The mixture wasextracted with ethyl acetate (3×). The combined organic phases weredried over Extrelut NT3, concentrated under reduced pressure and thecrude product was purified by preparative HPLC (method 7) to yield 14.2mg (24%) of the desired product.

LC-MS (method 10): R_(t)=1.64 min; MS (ESIpos): m/z=443 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.66), 0.008(1.67), 1.469 (16.00), 2.069 (10.83), 2.274 (2.96), 2.744 (11.16), 3.694(8.30), 4.861 (3.57), 7.893 (15.74), 8.469 (0.81), 9.457 (1.64).

Example 299 ethyl1-(6-{[5-(4-cyanophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

A microwave vial was charged ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (250mg, 891 μmol), 4-(3-amino-1,4-dimethyl-1H-pyrazol-5-yl)benzonitrile (208mg, 980 μmol) and sodium phenolate (155 mg, 1.34 mmol) and the contentswere suspended in 1,4-dioxane (4.0 ml, 46 mmol). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylidenaceton)dipalladium(10.6 mg, 11.6 μmol) and Xantphos (15.5 mg, 26.7 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously stirring. After coolingto ambient temperature, the reaction mixture was diluted with water andextracted with ethyl acetate (2×). The combined organic phases werewashed with water and brine, dried over sodium sulfate and concentratedunder reduced pressure. The crude product was purified by preparativeHPLC (method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 50mL/min/solvent: A=water (0.01% formic acid), B=acetonitrile/gradient:0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75 min=100% B, 19.75-23.00min=90% B) to yield the desired product (47.6 mg, 12%).

LC-MS (method 9): R_(t)=1.08 min; MS (ESIpos): m/z=457 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.291 (4.38), 1.309(8.89), 1.326 (4.48), 1.796 (0.46), 1.894 (13.15), 1.909 (1.58), 2.384(14.88), 2.891 (15.59), 3.163 (0.41), 3.177 (0.43), 3.489 (0.45), 3.734(16.00), 4.230 (1.40), 4.248 (4.13), 4.266 (4.07), 4.284 (1.35), 7.432(1.35), 7.699 (4.49), 7.719 (5.04), 8.004 (4.95), 8.025 (4.31), 8.534(3.31), 9.641 (2.47).

Example 3004-[3-({6-[4-(2-hydroxypropan-2-yl)-3,5-dimethyl-1H-pyrazol-1-yl]pyrimidin-4-yl}amino)-1,4-dimethyl-1H-pyrazol-5-yl]benzonitrile

A solution of ethyl1-(6-{[5-(4-cyanophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(38.0 mg, 83.2 μmol) in tetrahydrofuran (2.0 ml, 25 mmol) was treated at0° C. with a solution of methylmagnesium bromide (97 μl, 3.0 M indiethyl ether, 290 μmol) and stirred overnight at ambient temperature.No conversion was observed. Additional 3.5 equivalents ofmethylmagnesium bromide (97 μl, 3.0 M in diethyl ether, 290 μmol) wereadded at 0° C. and it was stirred for 3 hours at room temperature. Noconversion was observed. The mixture was cooled to −18° C. and asolution of methyl lithium (104 μL, 0.17 mmol, 1.6 M in diethyl ether)was added. The mixture was stirred overnight at ambient temperature. Noconversion was observed. The mixture was left over the weekend, then asolution of methylmagnesium chloride (55 μl, 3.0 M in tetrahydrofuran,170 μmol) was added and the mixture was stirred overnight. The mixturewas diluted with methanol and potassium sodium tartrate solution, andextracted with ethyl acetate (3×). The combined organic phases weredried over Extrelut NT3, concentrated under reduced pressure and thecrude product was purified by preparative HPLC (method 7) to yield 4.40mg (12%) of the desired product.

LC-MS (method 10): R_(t)=1.62 min; MS (ESIpos): m/z=443 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.63), 0.008(1.59), 1.472 (16.00), 1.887 (7.33), 2.277 (7.95), 2.717 (8.35), 3.726(8.40), 4.842 (3.17), 7.331 (0.89), 7.694 (2.18), 7.715 (2.54), 8.002(2.45), 8.022 (2.15), 8.458 (1.55), 9.440 (1.45).

Example 3014-[4-({6-[4-(2-hydroxy-2-methylpropyl)-3,5-dimethyl-1H-pyrazol-1-yl]pyrimidin-4-yl}amino)-3,5-dimethyl-1H-pyrazol-1-yl]benzonitrile

A solution of ethyl[1-(6-{[1-(4-cyanophenyl)-3,5-dimethyl-1H-pyrazol-4-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]acetate(162 mg, 344 μmol) in tetrahydrofuran (3.5 ml, 43 mmol) was treated witha solution of chloro(methyl)magnesium (400 μl, 3.0 M in tetrahydrofuran,1.2 mmol) at 0° C. and stirred 2 hours at ambient temperature. Themixture was diluted with water and extracted with ethyl acetate. Thecombined organic phases were dried over Extrelut NT3 and concentratedunder reduced pressure. The crude product was purified by preparativeHPLC (method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 50mL/min/solvent: A=water (0.01% formic acid), B=acetonitrile/gradient:0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75 min=100% B, 19.75-23.00min=90% B) and subsequently by flash-chromatography on silica gel(column: Biotage SNAP KP-Sil 19 g, solvent: 100% dichloromethane to 96%dichloromethane/4% methanol) to yield 43.4 mg (28%) of the desiredproduct.

LC-MS (method 10): R_(t)=1.65 min; MS (ESIpos): m/z=457 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.66), 0.008(0.66), 1.074 (3.98), 1.085 (16.00), 1.091 (9.62), 1.108 (2.57), 2.104(15.72), 2.158 (2.13), 2.294 (11.41), 2.425 (3.97), 2.563 (14.99), 3.357(0.73), 3.375 (2.10), 3.392 (2.08), 3.410 (0.68), 4.232 (3.48), 7.810(1.95), 7.831 (2.44), 7.978 (3.94), 7.999 (3.11), 8.387 (0.55), 8.881(3.50).

Example 3021-[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]-2-methylpropan-2-ol

A solution ethyl[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]acetate(570 mg, 1.13 mmol) in tetrahydrofuran (12 ml, 140 mmol) was treatedwith chloro(methyl)magnesium (1.3 ml, 3.0 M, 4.0 mmol) at 0° C. andstirred for 2 hours at ambient temperature. The mixture was diluted withpotassium sodium tartrate and water, and extracted with ethyl acetate(3×). The combined organic phases were washed with water, dried oversodium sulfate and concentrated under reduced pressure. The crudeproduct was purified by flash-chromatography on silica gel (column:Biotage SNAP Ultra 25 g, solvent: dichloromethane/methanol 20:1) andsubsequently by preparative HPLC (column: 250×20 mm YMC ChiralartCellulose SC, 5 μM, flow: 15 mL/min, solvent: n-heptane 30%/ethanol 70%)to yield 193 mg (35%) of the desired product along with its by-product1-[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]propan-2-one.

LC-MS (method 10): R_(t)=2.10 min; MS (ESIpos): m/z=490 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.006 (0.78), 0.007(0.58), 0.295 (2.10), 0.305 (2.23), 0.425 (2.19), 0.441 (2.27), 1.086(16.00), 1.183 (0.63), 1.188 (0.62), 1.198 (0.96), 1.207 (0.62), 1.212(0.62), 2.009 (13.17), 2.160 (2.07), 2.429 (3.79), 2.577 (14.87), 3.308(1.52), 3.324 (2.11), 3.329 (0.91), 3.829 (1.78), 3.842 (1.73), 4.237(3.72), 7.255 (1.97), 7.273 (3.97), 7.291 (2.13), 7.719 (1.26), 7.730(1.70), 7.746 (1.21), 8.449 (0.55), 9.319 (0.56).

Example 303 ethyl4-chloro-1-(6-{[4-chloro-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate

4-chloro-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (200 mg, 886μmol) and sodium phenolate (103 mg, 886 μmol) were suspended in1,4-dioxane (1.9 mL). The reaction mixture was degassed with Ar for 3min. Tris(dibenzylideneacetone)dipalladium (9.59 mg, 10.5 μmol) andXantPhos (14.0 mg, 24.2 μmol) and ethyl4-chloro-1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate(324 mg, 75% purity, 806 μmol) were added and the reaction mixture wasdegassed again for 1 min. The reaction mixture was heated at 90° C.overnight while vigorously stirring. After cooling to ambienttemperature, the reaction mixture was loaded onto silica gel andpurified by flash column chromatography (SNAP Ultra 25 g,cyclohexane/ethyl acetate gradient 95/5 to 20/80) to yield the desiredproduct (188 mg, 43% yield).

LC-MS (method 10): R_(t)=2.37 min; MS (ESIpos): m/z=490 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.89), 0.008(1.79), 1.157 (0.41), 1.175 (0.85), 1.193 (0.44), 1.227 (4.68), 1.245(10.15), 1.254 (0.99), 1.263 (5.09), 1.309 (0.78), 1.326 (1.42), 1.345(0.69), 1.398 (1.94), 1.989 (1.47), 2.284 (14.88), 2.328 (0.44), 2.675(2.50), 3.737 (0.66), 3.778 (16.00), 4.324 (1.51), 4.342 (4.75), 4.360(4.71), 4.378 (1.49), 7.202 (3.33), 7.384 (0.45), 7.411 (2.14), 7.433(4.72), 7.455 (2.64), 7.633 (2.51), 7.639 (1.15), 7.647 (2.82), 7.655(2.43), 7.669 (2.15), 8.451 (3.07), 8.597 (0.41), 9.860 (2.15).

Example 3042-[4-chloro-1-(6-{[4-chloro-5-(4-fluorophenyl)-1-methyl-1-pyrazol-3-yl]amino}pyrimidin-4-yl)-3-methyl-1H-pyrazol-5-yl]propan-2-ol

Under an argon atmosphere, ethyl4-chloro-1-(6-{[4-chloro-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate(188 mg, 383 μmol) was dissolved in tetrahydrofuran (7.6 mL) and thesolution cooled to 0° C. A solution of bromo(methyl)magnesium (1.9 ml,1.0 M, 1.9 mmol) was added dropwise and the reaction mixture was stirredovernight at ambient temperature. The reaction mixture was carefullyquenched by addition of aqueous Na₂EDTA solution (10%) and ethyl acetatewas added. After standing overnight, the organic phase was decanted andconcentrated. The residue was purified by flash column chromatography(SNAP Ultra 25 g, cyclohexane/ethyl acetate gradient 95/5 to 5/95) andfurther by preparative HPLC (method 6) to yield the desired product (22mg, 24% yield).

LC-MS (method 10): R_(t)=2.26 min; MS (ESIpos): m/z=476 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.71), 1.600(16.00), 2.190 (9.16), 3.762 (9.96), 6.691 (1.14), 7.154 (2.09), 7.407(1.21), 7.429 (2.69), 7.451 (1.52), 7.623 (1.48), 7.636 (1.66), 7.645(1.50), 7.658 (1.26), 8.562 (2.19), 9.884 (0.89).

Example 305N-{1-(cyclopropylmethyl)-3-[4-(difluoromethyl)phenyl]-4-methyl-1H-pyrazol-5-yl}-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (56.1 mg, 269 μmol)and1-(cyclopropylmethyl)-344-(difluoromethyl)phenyl1-4-methyl-1H-pyrazol-5-amine(82.0 mg, 296 μmol) and the contents were suspended in 1,4-dioxane (1.1ml, 13 mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (7.38 mg, 8.06 μmol) and Xantphos(9.33 mg, 16.1 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (34.3 mg, 296 μmol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was purified by preparativeHPLC (method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 50mL/min/solvent: A=water (0.01% formic acid), B=acetonitrile/gradient:0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75 min=100% B, 19.75-23.00min=90% B) and subsequently by flash-chromatography in silica gel(column; Biotage SNAP KP-Sil 10 g, solvent: 92% dichloromethane/8% ethylacetate to 66% ethyl acetate) to yield the desired product (44.3 mg,37%).

LC-MS (method 10): R_(t)=2.29 min; MS (ESIpos): m/z=450 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.49), 0.008(0.41), 0.305 (2.63), 0.316 (2.87), 0.431 (2.63), 0.451 (2.81), 1.074(0.69), 1.091 (1.44), 1.109 (0.73), 1.193 (0.71), 1.200 (0.70), 1.211(1.09), 1.223 (0.67), 1.231 (0.71), 2.050 (16.00), 2.170 (3.20), 2.631(15.46), 3.375 (0.72), 3.392 (0.72), 3.853 (2.58), 3.870 (2.52), 6.143(2.92), 6.938 (1.56), 7.078 (3.22), 7.218 (1.41), 7.637 (3.22), 7.657(3.95), 7.848 (3.13), 7.867 (2.63), 8.468 (0.78), 9.395 (0.84).

Example 306N-{1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethyl)phenyl]-1H-pyrazol-5-yl}-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged with1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethyl)phenyl]-1H-pyrazol-5-amine(131 mg, 90% purity, 401 μmol) and sodium phenolate (46.5 mg, 401 μmol)and the contents were suspended in 1,4-dioxane (0.9 mL). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (6.67 mg, 7.28 μmol), XantPhos(8.43 mg, 14.6 μmol) and4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (80.0 mg, 95%purity, 364 μmol), were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 90° C. overnightwhile vigorously shaking. After cooling to ambient temperature, thereaction mixture was filtered and concentrated. The residue wasredissolved in dimethylsulfoxide and purified by preparative HPLC(method 3) to yield the desired product (40 mg, 23% yield).

LC-MS (method 10): R_(t)=2.49 min; MS (ESIpos): m/z=468 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.36), −0.008(2.73), 0.008 (2.58), 0.146 (0.33), 0.306 (2.65), 0.317 (2.86), 0.434(2.83), 0.453 (2.99), 0.951 (0.19), 1.181 (0.41), 1.194 (0.78), 1.200(0.78), 1.212 (1.19), 1.223 (0.74), 1.231 (0.75), 2.068 (16.00), 2.284(1.93), 2.324 (0.79), 2.328 (0.81), 2.367 (0.36), 2.670 (0.45), 2.704(0.30), 2.711 (0.30), 3.871 (2.16), 3.887 (2.16), 6.788 (2.44), 7.684(1.56), 7.795 (3.28), 7.819 (5.96), 7.938 (2.39), 7.956 (3.42), 8.500(0.44), 9.579 (0.36).

Example 307N-{1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethyl)phenyl]-1H-pyrazol-5-yl}-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-amine

1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethyl)phenyl]-1H-pyrazol-5-amine(126 mg, 90% purity, 384 μmol) and sodium phenolate (44.6 mg, 384 μmol)were suspended in 1,4-dioxane (0.84 mL). The reaction mixture wasdegassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (6.40mg, 6.99 μmol), XantPhos (8.09 mg, 14.0 μmol) and4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (90.0mg, 95% purity, 350 μmol) were added and the reaction mixture wasdegassed again for 1 min. The vial was sealed and heated at 90° C.overnight while vigorously shaking. After cooling to ambienttemperature, the reaction mixture was filtered and concentrated. Theresidue was redissolved in dimethylsulfoxide and purified by preparativeHPLC (method 4) to yield the desired product (37 mg, 21% yield).

LC-MS (method 10): R_(t)=2.51 min; MS (ESIpos): m/z=504 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (2.86), 0.008(2.70), 0.307 (2.43), 0.319 (2.69), 0.434 (2.44), 0.453 (2.62), 1.196(0.65), 1.202 (0.63), 1.214 (1.01), 1.226 (0.63), 1.232 (0.63), 2.064(16.00), 2.172 (3.06), 2.328 (0.43), 2.631 (14.66), 2.670 (0.47), 3.863(2.42), 3.881 (2.38), 6.145 (2.64), 7.792 (3.04), 7.812 (4.11), 7.933(2.94), 7.953 (2.30), 8.469 (0.69), 9.412 (0.78).

Example 308N-{1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-5-yl}-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-5-amine(139 mg, 90% purity, 401 μmol) and sodium phenolate (46.5 mg, 401 μmol)were suspended in 1,4-dioxane (0.88 mL). The reaction mixture wasdegassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (6.67mg, 7.28 μmol), XantPhos (8.43 mg, 14.6 μmol) and4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (80.0 mg, 95%purity, 364 μmol) were added and the reaction mixture was degassed againfor 1 min. The vial was sealed and heated at 90° C. overnight whilevigorously shaking. After cooling to ambient temperature, the reactionmixture was filtered and concentrated. The residue was redissolved indimethylsulfoxide and purified by preparative HPLC (method 3) to yieldthe desired product (42 mg, 23% yield).

LC-MS (method 10): R_(t)=2.51 min; MS (ESIpos): m/z=484 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.45), −0.008(3.69), 0.008 (3.48), 0.298 (2.61), 0.310 (2.88), 0.425 (2.68), 0.445(2.84), 1.181 (0.72), 1.200 (1.09), 1.219 (0.66), 2.032 (16.00), 2.168(3.42), 2.328 (0.55), 2.367 (0.46), 2.630 (15.80), 2.670 (0.61), 2.710(0.52), 3.841 (2.56), 3.858 (2.55), 6.143 (3.03), 7.428 (3.32), 7.449(3.74), 7.820 (3.05), 7.842 (2.84), 8.464 (0.80), 9.390 (0.84).

Example 309N-{1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-5-yl}-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-amine

1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-5-amine(133 mg, 90% purity, 384 μmol) and sodium phenolate (44.6 mg, 384 μmol)were suspended in 1,4-dioxane (0.84 mL).

The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (6.40 mg, 6.99 μmol), XantPhos(8.09 mg, 14.0 μmol) and4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (90.0mg, 95% purity, 350 μmol) were added and the reaction mixture wasdegassed again for 1 min. The vial was sealed and heated at 90° C.overnight while vigorously shaking. After cooling to ambienttemperature, the reaction mixture was filtered and concentrated. Theresidue was redissolved in dimethylsulfoxide and purified by preparativeHPLC (method 3) to yield the desired product (49 mg, 26% yield).

LC-MS (method 10): R_(t)=2.50 min; MS (ESIpos): m/z=520 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.42), −0.008(3.56), 0.008 (3.09), 0.146 (0.40), 0.295 (2.95), 0.306 (3.15), 0.425(3.13), 0.445 (3.27), 1.165 (0.46), 1.178 (0.87), 1.185 (0.84), 1.197(1.28), 1.216 (0.82), 2.035 (16.00), 2.280 (2.18), 2.327 (0.90), 2.366(0.57), 2.670 (0.50), 2.702 (0.28), 2.710 (0.47), 3.847 (2.39), 3.864(2.36), 6.784 (2.56), 7.431 (3.50), 7.451 (3.88), 7.682 (1.68), 7.818(5.14), 7.843 (2.14), 7.954 (1.53), 8.496 (0.44), 9.569 (0.37).

Example 3106-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-{1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-5-yl}pyrimidin-4-amine

A microwave vial was charged with4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (80.0 mg,95% purity, 313 μmol),1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-5-amine(119 mg, 90% purity, 344 μmol) and sodium phenolate (39.9 mg, 344 μmol)and the contents were suspended in 1,4-dioxane (1.0 mL). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (5.73 mg, 6.25 μmol) and XantPhos(7.24 mg, 12.5 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously shaking. After cooling to ambient temperature, thereaction mixture was filtered and concentrated. The residue wasredissolved in dimethylsulfoxide and purified by preparative HPLC(method 3) to yield the desired product (47 mg, 29% yield).

LC-MS (method 10): R_(t)=2.74 min; MS (ESIpos): m/z=518 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.27), −0.008(2.20), 0.008 (2.08), 0.146 (0.24), 0.295 (2.17), 0.306 (2.37), 0.424(2.20), 0.444 (2.33), 1.179 (0.60), 1.197 (0.92), 2.030 (14.01), 2.208(2.29), 2.328 (0.34), 2.367 (0.28), 2.648 (16.00), 2.670 (0.54), 2.711(0.32), 3.841 (2.05), 3.859 (1.99), 7.429 (2.78), 7.450 (3.05), 7.819(2.28), 7.840 (2.14), 8.500 (0.51), 9.489 (0.42).

Example 3116-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-{1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethyl)phenyl]-1H-pyrazol-5-yl}pyrimidin-4-amine

A microwave vial was charged with4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (80.0 mg,95% purity, 313 μmol),1-(cyclopropylmethyl)-4-methyl-3-[4-(trifluoromethyl)phenyl]-1H-pyrazol-5-amine(113 mg, 90% purity, 344 μmol) and sodium phenolate (39.9 mg, 344 μmol)and the contents were suspended in 1,4-dioxane (0.75 mL). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (5.73 mg, 6.25 μmol) and XantPhos(7.24 mg, 12.5 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was filtered and concentrated. The residue wasredissolved in dimethylsulfoxide and purified by preparative HPLC(method 3) to yield the desired product (30 mg, 19% yield).

LC-MS (method 10): R_(t)=2.72 min; MS (ESIpos): m/z=502 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.61), −0.008(7.03), 0.008 (4.63), 0.146 (0.57), 0.306 (2.13), 0.317 (2.23), 0.432(2.21), 0.452 (2.23), 1.192 (0.63), 1.210 (0.89), 1.893 (0.16), 2.062(13.54), 2.212 (2.36), 2.328 (0.69), 2.366 (0.41), 2.524 (2.25), 2.650(16.00), 2.670 (0.89), 2.710 (0.45), 3.593 (0.18), 3.863 (2.05), 3.881(1.89), 7.792 (2.76), 7.813 (3.55), 7.931 (2.50), 7.951 (1.89), 8.502(0.49), 9.511 (0.45).

Example 312N-[3-(4-chlorophenyl)-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-5-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (109 mg, 521 μmol),3-(4-chlorophenyl)-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-5-amine(150 mg, 573 μmol) and sodium phenolate (66.5 mg, 573 μmol) and thecontents were suspended in 1,4-dioxane (3.0 ml, 35 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (6.20 mg, 6.77 μmol) and Xantphos(9.04 mg, 15.6 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was filtered and purified by preparative HPLC (method4) to yield the desired product (123 mg, 54%).

LC-MS (method 10): R_(t)=2.45 min; MS (ESIpos): m/z=434 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.67), 0.008(0.63), 0.295 (2.51), 0.306 (2.77), 0.318 (0.82), 0.424 (2.53), 0.444(2.70), 1.180 (0.67), 1.187 (0.66), 1.199 (1.05), 1.211 (0.63), 1.218(0.64), 2.019 (16.00), 2.074 (0.55), 2.169 (3.20), 2.629 (15.37), 3.833(2.50), 3.850 (2.47), 6.141 (2.82), 7.491 (4.49), 7.512 (5.61), 7.720(3.36), 7.742 (2.89), 8.461 (0.66), 9.381 (0.77).

Example 313N-[3-(4-chlorophenyl)-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-5-yl]-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-amine

A microwave vial was charged4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (127mg, 521 μmol),3-(4-chlorophenyl)-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-5-amine(150 mg, 573 μmol) and sodium phenolate (66.5 mg, 573 μmol) and thecontents were suspended in 1,4-dioxane (3.0 ml, 35 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (6.20 mg, 6.77 μmol) and Xantphos(9.04 mg, 15.6 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was filtered and purified by preparative HPLC (method4) to yield the desired product (102 mg, 40%).

LC-MS (method 10): R_(t)=2.48 min; MS (ESIpos): m/z=470 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.56), 0.008(1.54), 0.292 (2.69), 0.304 (2.90), 0.424 (2.87), 0.444 (3.05), 1.074(0.50), 1.091 (1.06), 1.109 (0.53), 1.165 (0.43), 1.177 (0.80), 1.184(0.79), 1.196 (1.22), 1.208 (0.75), 1.215 (0.77), 2.022 (16.00), 2.086(2.34), 2.283 (2.03), 2.328 (0.62), 2.701 (0.42), 3.375 (0.53), 3.392(0.53), 3.840 (2.22), 3.856 (2.18), 6.784 (2.50), 7.494 (4.28), 7.515(5.14), 7.682 (1.70), 7.724 (2.43), 7.744 (2.11), 7.818 (3.43), 7.953(1.46), 8.491 (0.42).

Example 314 ethyl1-(6-{[3-(4-chlorophenyl)-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

A microwave vial was charged ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (244mg, 868 μmol),3-(4-chlorophenyl)-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-5-amine(250 mg, 955 μmol) and sodium phenolate (111 mg, 955 μmol) and thecontents were suspended in 1,4-dioxane (5.0 ml, 58 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (10.3 mg, 11.3 μmol) and Xantphos(15.1 mg, 26.0 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was filtered and purified by preparative HPLC (method4) to yield the desired product (147 mg, 33%).

LC-MS (method 10): R_(t)=2.57 min; MS (ESIpos): m/z=506 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.07), 0.008(0.79), 0.296 (2.60), 0.308 (2.81), 0.427 (2.69), 0.447 (2.84), 1.182(0.73), 1.189 (0.71), 1.201 (1.10), 1.212 (0.67), 1.220 (0.69), 1.287(3.57), 1.305 (7.21), 1.323 (3.62), 2.020 (16.00), 2.329 (0.54), 2.369(2.17), 2.524 (0.46), 2.910 (12.58), 3.837 (2.27), 3.854 (2.24), 4.228(1.08), 4.246 (3.23), 4.263 (3.21), 4.281 (1.10), 7.491 (4.46), 7.512(5.52), 7.716 (3.22), 7.737 (2.79).

Example 315N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methoxy-1H-pyrazol-5-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (100 mg, 479 μmol)and1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methoxy-1H-pyrazol-5-amine(138 mg, 527 μmol) and the contents were suspended in 1,4-dioxane (2.0ml, 23 mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (13.2 mg, 14.4 μmol) and Xantphos(16.6 mg, 28.8 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (61.2 mg, 527 μmol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was purified by preparativeHPLC (method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 50mL/min/solvent: A=water (0.01% formic acid), B=acetonitrile/gradient:0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75 min=100% B,19.75-23.00min=90% B) and subsequently by flash-chromatography on silicagel (column: Biotage SNAP KP-Sil 10 g, solvent: 92% dichloromethane/8%ethyl acetate to 66% ethyl acetate) to yield the desired product (82.4mg, 40%).

LC-MS (method 10): R_(t)=2.29 min; MS (ESIpos): m/z=434 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.32), 0.008(1.28), 0.287 (0.50), 0.299 (2.08), 0.302 (1.83), 0.313 (2.18), 0.324(0.74), 0.429 (0.68), 0.439 (1.71), 0.443 (1.72), 0.449 (1.02), 0.459(1.85), 0.463 (1.68), 0.475 (0.56), 1.177 (0.45), 1.185 (0.44), 1.197(0.69), 1.209 (0.41), 1.216 (0.43), 2.167 (3.15), 2.633 (10.14), 3.641(0.50), 3.684 (16.00), 3.765 (1.81), 3.783 (1.78), 6.146 (2.30), 7.243(1.71), 7.266 (3.48), 7.288 (1.84), 7.883 (1.47), 7.897 (1.70), 7.905(1.67), 7.919 (1.40), 8.484 (1.05), 9.435 (0.76).

Example 3164-[1-(cyclopropylmethyl)-5-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-4-methoxy-1H-pyrazol-3-yl]benzonitrile

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (100 mg, 479 μmol)and4-[5-amino-1-(cyclopropylmethyl)-4-methoxy-1H-pyrazol-3-yl]benzonitrile(141 mg, 527 μmol) and the contents were suspended in 1,4-dioxane (2.0ml, 23 mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (13.2 mg, 14.4 μmol) and Xantphos(16.6 mg, 28.8 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (61.2 mg, 527 μmol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was purified by preparativeHPLC (method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 50mL/min/solvent: A=water (0.01% formic acid), B=acetonitrile/gradient:0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75 min=100% B,19.75-23.00min=90% B) and subsequently by flash-chromatography on silicagel (column: Biotage SNAP KP-Sil 10 g, solvent: 92% dichloromethane/8%ethyl acetate to 66% ethyl acetate) to yield the desired product (107mg, 51%).

LC-MS (method 10): R_(t)=2.21 min; MS (ESIpos): m/z=441 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.302 (0.76), 0.314(3.29), 0.328 (3.59), 0.340 (1.10), 0.442 (1.02), 0.452 (2.67), 0.456(2.68), 0.472 (2.89), 0.476 (2.69), 0.488 (0.80), 1.194 (0.80), 1.201(0.70), 1.212 (1.08), 1.224 (0.67), 1.231 (0.73), 2.172 (5.11), 2.634(16.00), 3.314 (13.53), 3.800 (2.97), 3.818 (2.94), 6.151 (3.61), 7.878(4.40), 7.899 (5.68), 8.049 (5.34), 8.070 (4.23), 8.488 (1.70), 9.487(1.33).

Example 317 1-[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methoxy-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]ethanone

A microwave vial was charged1-[1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]ethanone (200mg, 798 μmol) and1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methoxy-1H-pyrazol-5-amine(229 mg, 878 μmol) and the contents were suspended in 1,4-dioxane (3.3ml, 39 mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (21.9 mg, 23.9 μmol) and Xantphos(27.7 mg, 47.9 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (102 mg, 878 μmol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was purified by preparativeHPLC (method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 50mL/min/solvent: A=water (0.01% formic acid), B=acetonitrile/gradient:0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75 min=100% B,19.75-23.00min=90% B) to yield the desired product (168 mg, 44%).

LC-MS (method 10): R_(t)=2.10 min; MS (ESIpos): m/z=476 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.292 (0.92), 0.305(4.59), 0.317 (5.04), 0.328 (1.30), 0.435 (1.20), 0.446 (3.86), 0.466(4.07), 0.480 (0.90), 1.091 (0.63), 1.173 (0.64), 1.184 (0.98), 1.191(1.04), 1.203 (1.38), 1.213 (0.93), 1.221 (0.95), 1.233 (0.52), 2.464(13.99), 2.895 (16.00), 3.314 (12.54), 3.775 (3.52), 3.792 (3.48), 7.245(2.65), 7.267 (5.07), 7.289 (2.62), 7.879 (2.78), 7.894 (3.55), 7.899(3.47), 7.914 (2.62), 8.568 (1.52), 9.614 (0.87).

Example 3184-[5-{[6-(4-acetyl-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-1-(cyclopropylmethyl)-4-methoxy-1H-pyrazol-3-yl]benzonitrile

A microwave vial was charged1-[1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]ethanone (200mg, 798 μmol) and4-[5-amino-1-(cyclopropylmethyl)-4-methoxy-1H-pyrazol-3-yl]benzonitrile(235 mg, 878 μmol) and the contents were suspended in 1,4-dioxane (3.3ml, 39 mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (21.9 mg, 23.9 μmol) and Xantphos(27.7 mg, 47.9 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (102 mg, 878 μmol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was purified by preparativeHPLC (method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 50mL/min/solvent: A=water (0.01% formic acid), B=acetonitrile/gradient:0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75 min=100% B,19.75-23.00min=90% B) and subsequently by flash-chromatography on silicagel (column: Biotage SNAP KP-Sil 10 g, solvent: 92% dichloromethane/8%ethyl acetate to 66% ethyl acetate) to yield the desired product (177mg, 46%).

LC-MS (method 10): R_(t)=2.02 min; MS (ESIpos): m/z=483 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.309 (0.87), 0.321(3.83), 0.335 (4.06), 0.347 (1.23), 0.449 (1.17), 0.460 (3.11), 0.463(2.97), 0.469 (1.73), 0.479 (3.33), 0.495 (0.89), 1.159 (1.38), 1.177(2.84), 1.195 (1.73), 1.201 (0.88), 1.209 (0.81), 1.220 (1.26), 1.232(0.81), 1.239 (0.83), 1.251 (0.43), 1.990 (5.32), 2.467 (13.80), 2.898(16.00), 3.320 (8.34), 3.811 (2.90), 3.829 (2.86), 4.005 (0.46), 4.022(1.31), 4.040 (1.29), 4.058 (0.43), 7.878 (4.90), 7.899 (6.04), 8.047(6.24), 8.067 (4.79), 8.572 (1.33), 9.664 (0.75).

Example 319 ethyl1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methoxy-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

A microwave vial was charged ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (200mg, 712 μmol) and1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methoxy-1H-pyrazol-5-amine(205 mg, 784 μmol) and the contents were suspended in 1,4-dioxane (3.0ml, 35 mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (19.6 mg, 21.4 μmol) and Xantphos(24.7 mg, 42.7 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (91.0 mg, 784 μmol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was purified by preparativeHPLC (method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 50mL/min/solvent: A=water (0.01% formic acid), B=acetonitrile/grradient:0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75 min=100% B,19.75-23.00min=90% B) to yield the desired product (204 mg, 57%).

LC-MS (method 10): R_(t)=2.41 min; MS (ESIpos): m/z=506 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.295 (0.90), 0.309(4.61), 0.321 (5.13), 0.332 (1.36), 0.438 (1.18), 0.450 (3.89), 0.470(4.06), 0.483 (0.95), 1.075 (0.44), 1.093 (0.90), 1.110 (0.46), 1.178(0.91), 1.190 (1.01), 1.196 (1.15), 1.208 (1.41), 1.219 (0.97), 1.227(1.01), 1.238 (0.53), 1.287 (4.19), 1.304 (8.40), 1.322 (4.32), 1.992(0.74), 2.368 (4.80), 2.917 (16.00), 3.323 (5.52), 3.375 (0.44), 3.393(0.44), 3.778 (3.46), 3.795 (3.44), 4.226 (1.34), 4.244 (3.89), 4.261(3.87), 4.279 (1.34), 7.245 (2.52), 7.267 (5.05), 7.288 (2.80), 7.886(2.73), 7.901 (3.47), 7.907 (3.47), 7.922 (2.69), 8.564 (1.41), 9.610(0.89).

Example 320 ethyl1-(6-{[3-(4-cyanophenyl)-1-(cyclopropylmethyl)-4-methoxy-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

A microwave vial was charged ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (200mg, 712 μmol) and4-[5-amino-1-(cyclopropylmethyl)-4-methoxy-1H-pyrazol-3-yl]benzonitrile(210 mg, 784 μmol) and the contents were suspended in 1,4-dioxane (3.0ml, 35 mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (19.6 mg, 21.4 μmol) and Xantphos(24.7 mg, 42.7 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (91.0 mg, 784 μmol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was purified by preparativeHPLC (method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 50mL/min/solvent: A=water (0.01% formic acid), B=acetonitrile/grradient:0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75 min=100% B,19.75-23.00min=90% B) to yield the desired product (205 mg, 56%).

LC-MS (method 10): R_(t)=2.33 min; MS (ESIpos): m/z=513 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.307 (0.88), 0.319(3.88), 0.332 (4.15), 0.344 (1.22), 0.447 (1.17), 0.458 (3.16), 0.461(3.06), 0.478 (3.39), 0.493 (0.87), 1.075 (1.02), 1.092 (2.08), 1.110(1.06), 1.187 (0.46), 1.198 (0.86), 1.205 (0.83), 1.217 (1.27), 1.229(0.97), 1.236 (0.86), 1.248 (0.45), 1.289 (4.28), 1.306 (8.69), 1.324(4.37), 2.372 (4.05), 2.919 (16.00), 3.317 (9.20), 3.375 (1.01), 3.393(0.99), 3.807 (2.91), 3.824 (2.87), 4.229 (1.30), 4.246 (3.85), 4.264(3.82), 4.282 (1.28), 7.878 (4.67), 7.899 (5.89), 8.047 (5.94), 8.067(4.63), 8.566 (1.29), 9.654 (0.79).

Example 3214-[5-{[6-(4-acetyl-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile

This product was obtained as a by-product during the synthesis of4-[1-(cyclopropylmethyl)-5-({6-[4-(2-hydroxypropan-2-yl)-3,5-dimethyl-1H-pyrazol-1-yl]pyrimidin-4-yl}amino)-4-methyl-1H-pyrazol-3-yl]benzonitrile(see example 167) after purification by flash column chromatography(SNAP Ultra 10 g, dichloromethane/methanol gradient 99/1 to 95/5). Thetitle compound was obtained as an off-white solid after lyophilisation(55 mg, 10% yield).

LC-MS (method 10): R_(t)=1.97 min; MS (ESIpos): m/z=467 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.25), −0.008(2.06), 0.008 (2.10), 0.146 (0.23), 0.311 (2.49), 0.321 (2.74), 0.438(2.51), 0.457 (2.67), 1.181 (0.39), 1.194 (0.71), 1.201 (0.71), 1.213(1.08), 1.225 (0.74), 1.233 (0.94), 1.306 (0.25), 2.065 (16.00), 2.328(0.41), 2.467 (8.99), 2.608 (0.79), 2.670 (0.38), 2.890 (10.02), 2.914(0.58), 3.868 (2.26), 3.885 (2.23), 7.886 (0.72), 7.907 (13.49), 7.931(0.72), 8.026 (0.21), 8.540 (0.43), 9.588 (0.39).

Example 322(±)-4-{1-(cyclopropylmethyl)-5-[(6-{3,5-dimethyl-4-[(2S)-1,1,1-trifluoro-2-hydroxypropan-2-yl]-1H-pyrazol-1-yl}pyrimidin-4-yl)amino]-4-methyl-1H-pyrazol-3-yl}benzonitrile(racemate)

Molecular Sieves (4 Å) were placed in a round-bottom flask and dried ina vacuum drying-oven overnight at 120° C. After cooling to ambienttemperature, tetrabutylammonium fluoride trihydrate (132 mg, 472 μmol)and toluene (1.0 mL) were added and the suspension stirred for 30 min. Asolution of4-[5-{[6-(4-acetyl-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(55.0 mg, 118 μmol) in toluene (4.5 mL) was then added, the mixture wasstired for 5 min and cooled to 0° C. Trimethyl(trifluoromethyl)silane(100 μlt, 710 μmol) was then added and stirred at ambient temperaturefor 3.5 h. A second aliquot of trimethyl(trifluoromethyl)silane (60 μl,0.4 mmol) was added and the reaction mixture was stirred at ambienttemperature overnight. The reaction mixture was diluted with ethylacetate and water, the molecular sieves removed by filtration and washedfurther with ethyl acetate. After separation of the layers, the aqueousphase was extracted again with ethyl acetate and the combined organicphase were dried over sodium sulfate and concentrated. The residue waspurified by preparative HPLC (column: Chromatorex C18; 125*30 mm, 10 μM,flow 75 mL/min, gradient acetonitrile/water 5/95 to 90/10) to yield thedesired product (8 mg, 13% yield) along with a by-product((±)-2-{1-[6-({3-[4-(2-amino-1,1,1,3,3,3-hexafluoropropan-2-yl)phenyl]-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3,5-dimethyl-1H-pyrazol-4-yl}-1,1,1-trifluoropropan-2-ol(racemate)).

LC-MS (method 11): R_(t)=1.41 min; MS (ESIpos): m/z=537 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.48), −0.023(0.76), −0.008 (4.03), 0.146 (0.44), 0.306 (2.56), 0.317 (2.82), 0.433(2.50), 0.453 (2.68), 0.853 (0.30), 0.918 (0.30), 0.936 (0.82), 0.954(0.38), 1.209 (1.14), 1.234 (2.54), 1.764 (6.89), 2.061 (16.00), 2.272(2.50), 2.327 (0.98), 2.366 (0.42), 2.670 (1.00), 2.710 (0.54), 2.747(12.36), 3.860 (2.34), 3.878 (2.30), 5.754 (1.80), 6.437 (2.98), 7.881(0.88), 7.903 (13.26), 8.487 (0.64), 9.493 (0.62).

Example 323 tert-butyl3-[4-(5-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-1,4-dimethyl-1H-pyrazol-3-yl)phenyl]azetidine-1-carboxylate

In a microwave vial, (30.7 mg, 27.4 μmol),N-[3-(4-bromophenyl)-1,4-dimethyl-1H-pyrazol-5-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine(120 mg, 274 μmol), and lithium hydroxide (19.7 mg, 821 μmol) wereloaded. DME (5.5 mL) was then added.

The nickel pre-catalyst was then prepared in a second microwave vial. Tothis vial, nickel (II) chloride dimethoxyethane adduct (32.9 mg, 0.15mmol) and 4,4′-di-tert-butyl-2,2′-bipyridine (48.3 mg, 0.18 mmol) wereloaded and dissolved in DME (12 mL), placed under argon, sealed andsonicated for 5 minutes.

An aliquot of the nickel pre-catalyst solution just prepared (1.1 mL)was syringed into the vial containing the reactants. The solution wasdegassed a second time by sparging with argon while stirring for 10minutes. Under a constant flow of argon, tert-butyl3-bromoazetidine-1-carboxylate (220 μl, 1.4 mmol) and1,1,1,3,3,3-hexamethyl-2-(trimethylsilyl)trisilane (250 ∞l, 820 μmol)were then added to the reaction mixture using a Hamilton syringe. Themicrowave vial was then sealed with Parafilm, stirred and irradiatedwith two 34 W blue LED lamps (3 cm away) for 15 h. The reaction mixturewas concentrated and the residue dissolved in acetonitrile/water andpurified by preparative HPLC (column: Chromatorex C18; 125*30 mm, 10 μM,flow 75 mL/min, gradient acetonitrile/water (containing 0.1%trifluoroacetic acid) 30/70 to 95/5) to yield the desired product (60mg, 86% purity, 37% yield).

LC-MS (method 10): R_(t)=2.29 min; MS (ESIpos): m/z=515 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.20), −0.008(1.57), 0.008 (1.69), 0.082 (0.66), 0.146 (0.28), 1.169 (0.21), 1.366(0.34), 1.413 (16.00), 2.025 (4.55), 2.171 (1.11), 2.327 (0.34), 2.366(0.30), 2.523 (0.88), 2.630 (4.10), 2.669 (0.38), 2.710 (0.31), 3.662(3.05), 3.850 (0.73), 4.272 (0.49), 6.144 (0.81), 7.394 (0.98), 7.414(1.14), 7.635 (0.23), 7.643 (0.20), 7.667 (0.89), 7.687 (0.71), 8.472(0.26), 9.397 (0.59).

Example 324N-[3-(4-cyclopropylphenyl)-1,4-dimethyl-1H-pyrazol-5-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

In a microwave vial, (30.7 mg, 27.4 μmol),N-[3-(4-bromophenyl)-1,4-dimethyl-1H-pyrazol-5-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine(120 mg, 274 μmol), and lithium hydroxide (19.7 mg, 821 μmol) wereloaded. DME (5.5 mL) was then added.

The nickel pre-catalyst was then prepared in a second microwave vial. Tothis vial, nickel (II) chloride dimethoxyethane adduct (32.98 mg, 0.15mmol, 0.25 equiv.) and 4,4′-di-tert-butyl-2,2′-bipyridine (48.30 mg,0.18 mmol, 0.3 equiv.) were loaded and dissolved in DME (12 mL), placedunder argon, sealed and sonicated for 5 minutes.

An aliquot of the nickel pre-catalyst solution just prepared (1.1 mL)was syringed into the vial containing the reactants. The solution wasdegassed a second time by sparging with argon while stirring for 10minutes. Under a constant flow of argon, bromocyclopropane (110 μl, 1.4mmol) and 1,1,1,3,3,3-hexamethyl-2-(trimethylsilyl)trisilane (204 mg,821 μmol) were then added to the reaction mixture using a Hamiltonsyringe. The microwave vial was then sealed with Parafilm, stirred andirradiated with two 34 W blue LED lamps (3 cm away) for 15 hours. Thereaction mixture was concentrated, the residue was dissolved inacetonitrile/water and purified by preparative HPLC (column: ChromatorexC18; 125*30 mm, 10 μM, flow 75 mL/min, gradient acetonitrile/water(containing 0.1% trifluoroacetic acid) 30/70 to 95/5) to yield thedesired product (3.7 mg, 3% yield).

LC-MS (method 11): R_(t)=1.51 min; MS (ESIpos): m/z=400 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.150 (1.49), −0.008(11.36), 0.008 (13.32), 0.083 (6.78), 0.103 (5.12), 0.146 (2.80), 0.696(2.80), 0.708 (2.86), 0.889 (1.55), 0.960 (2.50), 0.975 (2.62), 1.117(1.72), 1.169 (2.86), 1.233 (1.55), 1.943 (1.25), 2.002 (14.45), 2.018(2.20), 2.168 (4.58), 2.327 (2.91), 2.366 (2.26), 2.628 (16.00), 2.669(2.86), 2.710 (2.20), 3.646 (9.99), 6.141 (3.27), 7.125 (3.81), 7.146(3.93), 7.547 (2.97), 7.567 (2.74), 8.469 (1.25), 9.379 (2.02).

Example 325(±)-2-cyclopropyl-1-[5-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-1-yl]propan-2-ol(racemate)

A microwave vial was charged with (2S)-1-[5-amino-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-1-yl]-2-cyclopropylpropan-2-ol(39.0 mg, 135 μmol), 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine(30.9 mg, 148 μmol) and sodium phenolate (17.2 mg, 148 μmol) and thecontents were suspended in 1,4-dioxane (0.5 mL). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium(2.47 mg, 2.70 μmol) and XantPhos (3.12 mg, 5.39 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously shaking. After coolingto ambient temperature, the reaction mixture was filtered andconcentrated. The residue was purified by flash column chromatography(SNAP Ultra 10 g, cyclohexane/ethyl acetate gradient 95/5 to 0/100) toyield the desired product (16 mg, 25% yield).

LC-MS (method 11): R_(t)=1.56 min; MS (ESIpos): m/z=462 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.126 (1.01), 0.147(0.97), 0.160 (0.85), 0.187 (1.20), 0.221 (2.77), 0.232 (2.90), 0.805(0.80), 0.812 (0.85), 0.826 (1.37), 0.839 (0.75), 0.846 (0.71), 1.085(14.07), 1.236 (0.43), 1.977 (0.41), 2.009 (16.00), 2.171 (5.84), 2.328(0.84), 2.629 (15.59), 2.670 (1.07), 2.710 (0.47), 3.984 (2.86), 4.511(0.91), 6.143 (3.57), 7.256 (2.30), 7.278 (4.83), 7.300 (2.77), 7.707(2.05), 7.721 (2.61), 7.728 (2.61), 7.742 (2.16), 8.462 (1.29), 9.199(2.98).

Example 326(±)-N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-{4-[1-methoxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-amine(racemic)

A solution of1-[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]ethanone(304 mg, 662 μmol) in methanol (12 ml, 290 mmol) was treated with sodiumborohydride (12.5 mg, 331 μmol). The mixture was stirred 2 hours atambient temperature. The mixture was treated with some drops ofconcentrated hydrochloric acid ans stirred overnight at ambienttemperature. The mixture was purified by preparative HPLC (method:column: Reprosil C18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent: A=water(0.01% formic acid), B=acetonitrile/grradient: 0.00-5.00 min=10% B, 6.50min=20% B, 17.0-19.75 min=100% B, 19.75-23.00 min=90% B) andsubsequently by flash-chromatography on silica gel (column: SNAP KP-Sil10 g, dichloromethane/ethyl acetate) to yield 102 mg (33%) of thedesired product along with traces of the corresponding.

LC-MS (method 9): R_(t)=1.18 min; MS (ESIpos): m/z=476 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.294 (2.78), 0.305(2.99), 0.425 (2.71), 0.444 (2.83), 1.177 (0.87), 1.185 (0.72), 1.197(1.10), 1.209 (0.70), 1.216 (0.70), 1.228 (0.40), 1.352 (5.16), 1.368(5.19), 1.990 (0.73), 2.009 (14.58), 2.202 (3.29), 2.502 (10.92), 2.636(16.00), 3.094 (12.53), 3.828 (2.51), 3.845 (2.52), 4.369 (0.47), 4.385(1.46), 4.401 (1.47), 4.418 (0.51), 7.252 (1.94), 7.274 (4.09), 7.296(2.29), 7.715 (1.58), 7.730 (2.18), 7.735 (2.22), 7.750 (1.69), 8.468(0.70), 9.377 (0.83).

Example 327N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-{4-[1-methoxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-amine

A sample of racemicN-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-{4-[1-methoxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-amine(101.5 mg, 0.21 mmol) was separated using SFC chromatography (column:AD-H; 250*20 mm, 5μM, flow 80 mL/min, 40° C., solvent 84% carbondioxide/16% 2-propanol) to give 25.6 mg of the first eluting enantiomerofN-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-{4-[1-methoxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-amine(25% yield from racemate).

LC-MS (method 10): R_(t)=2.29 min; MS (ESIpos): m/z=476 [M+H]⁺

Chiral HPLC (SFC, Daicel AD, Solvent: 80% carbon dioxide/20% 2-propanol)Rt=1.43 min, >99.5% enantiomeric excess.

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.06), 0.008(1.10), 0.292 (2.17), 0.304 (2.40), 0.423 (2.20), 0.443 (2.34), 1.177(0.59), 1.184 (0.58), 1.196 (0.92), 1.208 (0.56), 1.215 (0.57), 1.352(4.33), 1.368 (4.39), 2.008 (13.51), 2.201 (2.58), 2.635 (16.00), 3.093(11.64), 3.827 (2.21), 3.844 (1.99), 4.369 (0.41), 4.385 (1.29), 4.402(1.28), 4.418 (0.41), 7.252 (2.01), 7.274 (4.12), 7.296 (2.24), 7.713(1.43), 7.728 (1.81), 7.734 (1.78), 7.749 (1.32), 8.466 (0.59), 9.375(0.64).

Example 328N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-{4-[1-methoxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-amine

A sample of racemicN-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-{4-[1-methoxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-amine(101.5 mg, 0.21 mmol) was separated using SFC chromatography (column:AD-H; 250*20 mm, 5 μM, flow 80 mL/min, 40° C., solvent 84% carbondioxide/16% 2-propanol) to give 25.0 mg of the second eluting enantiomerofN-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-{4-[1-methoxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-amine (25% yield fromracemate).

LC-MS (method 10): R_(t)=2.29 min; MS (ESIpos): m/z=476 [M+H]⁺

Chiral HPLC (SFC, Daicel AD, Solvent: 80% carbon dioxide/20% 2-propanol)Rt=1.43 min, >98.1% enantiomeric excess.

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.91), 0.008(1.00), 0.292 (2.27), 0.304 (2.49), 0.424 (2.26), 0.443 (2.42), 1.178(0.60), 1.185 (0.61), 1.196 (0.96), 1.209 (0.60), 1.215 (0.59), 1.352(4.42), 1.368 (4.47), 2.008 (13.57), 2.201 (2.74), 2.635 (16.00), 3.093(11.77), 3.827 (2.10), 3.844 (2.09), 4.369 (0.42), 4.385 (1.31), 4.401(1.31), 4.418 (0.43), 7.252 (2.02), 7.274 (4.19), 7.296 (2.27), 7.714(1.45), 7.728 (1.90), 7.735 (1.87), 7.749 (1.41), 8.465 (0.67), 9.376(0.68).

Example 3291-[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]ethanol

A sample of racemic1-[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]ethanol(100.4 mg, 0.18 mmol) was separated using SFC chromatography (column:AD-H; 250*20 mm, 5 μM, flow 80 mL/min, 40° C., solvent 84% carbondioxide/16% 2-propanol) to give 8.5 mg of the first eluting enantiomerof1-[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]ethanol(9% yield from racemate) along with the methoxy derivative.

LC-MS (method 10): R_(t)=1.89 min; MS (ESIpos): m/z=462 [M+H]⁺

Chiral HPLC (SFC, Daicel AD, Solvent: 80% carbon dioxide/20% 2-propanol)Rt=1.43 min, >99.5% enantiomeric excess.

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.66), 0.008(1.47), 0.068 (0.69), 0.291 (2.28), 0.302 (2.49), 0.420 (2.24), 0.440(2.37), 1.030 (1.08), 1.045 (1.07), 1.176 (0.63), 1.182 (0.61), 1.194(0.94), 1.206 (0.59), 1.212 (0.59), 1.320 (4.52), 1.336 (4.57), 2.003(13.84), 2.234 (2.83), 2.631 (16.00), 3.824 (2.24), 3.841 (2.22), 4.765(0.76), 4.773 (0.84), 4.782 (0.79), 4.789 (0.82), 4.908 (2.01), 4.916(1.89), 7.251 (1.99), 7.273 (4.25), 7.295 (2.34), 7.712 (1.44), 7.726(1.89), 7.732 (1.90), 7.747 (1.47), 8.453 (0.71), 9.349 (0.68).

Example 3301-[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]ethanol

A sample of racemic1-[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]ethanol(100.4 mg, 0.18 mmol) was separated using SFC chromatography (column:AD-H; 250*20 mm, 5μM, flow 80 mL/min, 40° C., solvent 84% carbondioxide/16% 2-propanol) to give 9.4 mg of the second eluting enantiomerof1-[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]ethanol(9% yield from racemate) along with the methoxy derivative.

LC-MS (method 10): R_(t)=1.89 min; MS (ESIpos): m/z=462 [M+H]⁺

Chiral HPLC (SFC, Daicel AD, Solvent: 80% carbon dioxide/20% 2-propanol)Rt=1.43 min, >99.5% enantiomeric excess.

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.98), 0.008(0.90), 0.290 (2.30), 0.302 (2.53), 0.420 (2.28), 0.440 (2.42), 1.030(0.67), 1.045 (0.68), 1.175 (0.64), 1.182 (0.61), 1.194 (0.94), 1.206(0.58), 1.213 (0.59), 1.320 (4.69), 1.336 (4.74), 2.004 (14.03), 2.234(2.87), 2.632 (16.00), 3.824 (2.29), 3.841 (2.24), 4.765 (0.78), 4.773(0.87), 4.782 (0.82), 4.789 (0.83), 4.909 (2.05), 4.916 (1.91), 7.251(2.06), 7.273 (4.22), 7.295 (2.29), 7.712 (1.48), 7.726 (1.90), 7.732(1.84), 7.747 (1.40), 8.453 (0.69), 9.347 (0.71).

Example 331(±)-4-{1-(cyclopropylmethyl)-5-[(6-{4-[(1S)-1-hydroxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-yl)amino]-4-methoxy-1H-pyrazol-3-yl}benzonitrile(racemic)

A solution of4-[5-{[6-(4-acetyl-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-1-(cyclopropylmethyl)-4-methoxy-1H-pyrazol-3-yl]benzonitrile(144 mg, 298 μmol) in methanol (5.3 ml, 130 mmol) was treated withsodium borohydride (11.3 mg, 298 μmol). The mixture was stirred atambient temperature overnight. The mixture was diluted with water,dichloromethane and filtered over Extrelut NT3. The filtrate wasconcentrated under reduced pressure to yield 136 mg (93%) of the desiredproduct.

LC-MS (method 10): R_(t)=1.87 min; MS (ESIpos): m/z=485 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.300 (0.50), 0.312(2.08), 0.315 (1.88), 0.326 (2.20), 0.338 (0.73), 0.441 (0.69), 0.451(1.70), 0.455 (1.73), 0.461 (1.03), 0.471 (1.86), 0.475 (1.69), 0.486(0.53), 1.074 (1.60), 1.091 (3.26), 1.109 (1.65), 1.191 (0.45), 1.199(0.45), 1.211 (0.70), 1.223 (0.43), 1.230 (0.47), 1.322 (4.24), 1.338(4.28), 2.238 (3.05), 2.637 (12.13), 3.357 (0.58), 3.375 (1.64), 3.392(1.61), 3.410 (0.53), 3.725 (16.00), 3.798 (1.84), 3.815 (1.82), 4.770(0.66), 4.777 (0.72), 4.786 (0.68), 4.794 (0.70), 4.917 (1.73), 4.924(1.61), 7.876 (2.99), 7.898 (3.86), 8.046 (3.51), 8.067 (2.71), 8.478(1.02), 9.464 (0.53).

Example 3324-{1-(cyclopropylmethyl)-5-[(6-{4-[1-hydroxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-yl)amino]-4-methoxy-1H-pyrazol-3-yl}benzonitrile

A sample of racemic4-{1-(cyclopropylmethyl)-5-[(6-{4-[1-hydroxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-yl)amino]-4-methoxy-1H-pyrazol-3-yl}benzonitrile(102 mg, 0.21 mmol) was separated using SFC chromatography (column:AD-H; 250*20 mm, 5 μM, flow 80 mL/min, 40° C., solvent 78% carbondioxide/22% 2-propanol) to give 27.6 mg of the second eluting enantiomerof4-{1-(cyclopropylmethyl)-5-[(6-{4-[1-hydroxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-yl)amino]-4-methoxy-1H-pyrazol-3-yl}benzonitrile(27% yield from racemate) along with the first eluting enantiomer (34.2mg).

LC-MS (method 9): R_(t)=0.95 min; MS (ESIpos): m/z=485 [M+H]⁺

Chiral HPLC (SFC, Daicel AD-3, Solvent: 80% carbon dioxide/20%2-propanol) Rt=1.43 min, >99.5% enantiomeric excess.

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.16), 0.008(1.19), 0.299 (0.51), 0.311 (2.12), 0.314 (1.90), 0.325 (2.25), 0.337(0.72), 0.440 (0.69), 0.450 (1.73), 0.454 (1.75), 0.460 (1.01), 0.470(1.88), 0.474 (1.70), 0.486 (0.53), 1.190 (0.45), 1.197 (0.43), 1.209(0.70), 1.221 (0.41), 1.228 (0.44), 1.321 (4.32), 1.337 (4.36), 2.237(3.05), 2.524 (0.54), 2.636 (12.36), 3.723 (16.00), 3.796 (1.88), 3.814(1.86), 4.769 (0.68), 4.776 (0.74), 4.785 (0.69), 4.793 (0.72), 4.915(1.80), 4.923 (1.66), 7.877 (2.87), 7.898 (3.88), 8.044 (3.48), 8.066(2.75), 8.477 (0.97), 9.460 (0.81).

Example 333(±)-4-{1-(cyclopropylmethyl)-4-methoxy-5-[(6-{4-[1-methoxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-yl)amino]-1H-pyrazol-3-yl}benzonitrile(racemic)

A solution of4-{1-(cyclopropylmethyl)-5-[(6-{4-[1-hydroxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-yl)amino]-4-methoxy-1H-pyrazol-3-yl}benzonitrile(113 mg, 233 μmol) in methanol (5.0 ml, 120 mmol) and trifluoroaceticacid (500 μl, 6.5 mmol) was stirred at ambient temperature overnight.The mixture was concentrated and purified by flash-chromatography onsilica gel (column: SNAP KP-Sil 10 g, solvent: 92% dichloromethane/8%ethyl acetate to 66% ethyl acetate) to yield 78.1 mg (67%) of thedesired product.

LC-MS (method 10): R_(t)=2.22 min; MS (ESIpos): m/z=499 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.301 (0.69), 0.313(2.85), 0.327 (3.08), 0.338 (0.95), 0.442 (0.92), 0.453 (2.37), 0.457(2.38), 0.462 (1.39), 0.473 (2.57), 0.476 (2.34), 0.488 (0.70), 1.192(0.66), 1.199 (0.63), 1.211 (0.98), 1.223 (0.60), 1.230 (0.66), 1.353(5.51), 1.370 (5.55), 2.204 (3.92), 2.640 (16.00), 3.095 (15.00), 3.683(0.53), 3.799 (2.60), 3.816 (2.53), 4.373 (0.48), 4.389 (1.58), 4.406(1.56), 4.422 (0.47), 7.877 (4.12), 7.898 (5.25), 8.046 (4.87), 8.067(3.76), 8.491 (1.44), 9.492 (1.05).

Example 3344-{1-(cyclopropylmethyl)-4-methoxy-5-[(6-{4-[1-methoxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-yl)amino]-1H-pyrazol-3-yl}benzonitrile

A sample of racemic4-{1-(cyclopropylmethyl)-4-methoxy-5-[(6-{4-[1-methoxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-yl)amino]-1H-pyrazol-3-yl}benzonitrile(62 mg, 0.16 mmol) was separated using preparative HPLC (column: 250*20mm Daicel Chiralcel OJ-H, 5 μM, flow 15 mL/min, 40° C., solvent 85%n-Heptan/15% ethanol) to give 27.0 mg of the first eluting enantiomer of4-{1-(cyclopropylmethyl)-4-methoxy-5-[(6-{4-[1-methoxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-yl)amino]-1H-pyrazol-3-yl}benzonitrile(44% yield from racemate).

LC-MS (method 10): R_(t)=2.21 min; MS (ESIpos): m/z=499 [M+H]⁺

Chiral HPLC (Daicel Chiralcel OJ-H, 5 μM, flow 1 mL/min, solvent: 85%2-propanol/15% ethanol) Rt=4.8 min, >98% enantiomeric excess.

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.48), 0.301(0.66), 0.313 (2.38), 0.327 (2.44), 0.338 (0.76), 0.442 (0.86), 0.453(1.98), 0.457 (1.97), 0.462 (1.18), 0.473 (2.07), 0.477 (1.86), 0.488(0.57), 1.003 (0.97), 1.021 (1.94), 1.039 (0.98), 1.192 (0.56), 1.199(0.54), 1.211 (0.81), 1.223 (0.50), 1.230 (0.56), 1.353 (4.69), 1.370(4.61), 1.892 (2.54), 2.204 (3.21), 2.524 (0.75), 2.581 (0.84), 2.599(0.87), 2.617 (0.53), 2.640 (12.95), 3.095 (12.17), 3.728 (16.00), 3.799(2.03), 3.816 (1.92), 4.373 (0.44), 4.389 (1.35), 4.406 (1.31), 7.877(3.12), 7.898 (3.97), 8.046 (3.72), 8.067 (2.85), 8.491 (0.96).

Example 3354-{1-(cyclopropylmethyl)-4-methoxy-5-[(6-{4-[(1S)-1-methoxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-yl)amino]-1H-pyrazol-3-yl}benzonitrile

A sample of racemic 4-{1-(cyclopropylmethyl)-4-methoxy-5-[(6-{4-[1-methoxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-yl)amino]-1H-pyrazol-3-yl}benzonitrile(62 mg, 0.16 mmol) was separated using preparative HPLC (column: 250*20mm Daicel Chiralcel OJ-H, 5 μM, flow 15 mL/min, 40° C., solvent 85%n-Heptan/15% ethanol) to give 24.0 mg of the second eluting enantiomerof4-{1-(cyclopropylmethyl)-4-methoxy-5-[(6-{4-[1-methoxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-yl)amino]-1H-pyrazol-3-yl}benzonitrile(39% yield from racemate).

LC-MS (method 10): R_(t)=2.21 min; MS (ESIpos): m/z=499 [M+H]⁺

Chiral HPLC (Daicel Chiralcel OJ-H, 5 μM, flow 1 mL/min, solvent: 85%2-propanol/15% ethanol) Rt=5.3 min, >98% enantiomeric excess.

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.300 (0.46), 0.312(1.97), 0.327 (2.13), 0.338 (0.69), 0.442 (0.65), 0.453 (1.63), 0.457(1.63), 0.462 (0.92), 0.473 (1.78), 0.477 (1.63), 0.489 (0.52), 1.192(0.46), 1.199 (0.43), 1.211 (0.69), 1.223 (0.43), 1.231 (0.45), 1.353(4.04), 1.370 (4.12), 2.204 (2.79), 2.640 (12.17), 3.095 (11.56), 3.728(16.00), 3.799 (1.66), 3.816 (1.64), 4.389 (1.19), 4.406 (1.17), 7.877(3.05), 7.898 (3.96), 8.046 (3.58), 8.067 (2.76), 8.491 (1.08), 9.489(0.62).

Example 336(±)-1-[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methoxy-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]ethanol(racemate)

A solution of1-[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methoxy-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]ethanone(139 mg, 292 μmol) in methanol (5.0 ml, 120 mmol) was treated withsodium borohydride (11.0 mg, 292 μmol) and stirred 30 minutes at roomtemperature. The mixture was diluted with water, dichloromethane andfiltered over Extrelut NT3. The filtrate was concentrated to yield 133mg (93%) of the desired product.

LC-MS (method 10): R_(t)=1.95 min; MS (ESIpos): m/z=478 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.286 (0.55), 0.298(2.45), 0.311 (2.64), 0.324 (0.79), 0.429 (0.73), 0.439 (2.01), 0.443(1.93), 0.448 (1.10), 0.459 (2.15), 0.475 (0.56), 1.074 (1.09), 1.091(2.21), 1.109 (1.12), 1.178 (0.55), 1.186 (0.51), 1.197 (0.78), 1.209(0.48), 1.216 (0.51), 1.321 (4.78), 1.337 (4.82), 2.234 (3.66), 2.637(13.01), 3.375 (1.08), 3.392 (1.06), 3.680 (16.00), 3.764 (2.22), 3.781(2.18), 4.768 (0.75), 4.776 (0.82), 4.784 (0.77), 4.792 (0.78), 4.913(1.93), 4.920 (1.76), 7.243 (1.64), 7.265 (3.29), 7.287 (1.72), 7.881(1.65), 7.896 (1.96), 7.903 (1.86), 7.917 (1.53), 8.475 (1.13), 9.414(0.74).

Example 3374-(5-{[6-(4-acetyl-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-1,4-dimethyl-1H-pyrazol-3-yl)benzonitrile

A microwave vial was charged1-[1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]ethanone (250mg, 997 μmol) and 4-(5-amino-1,4-dimethyl-1H-pyrazol-3-yl)benzonitrile(233 mg, 1.10 mmol) and the contents were suspended in 1,4-dioxane (4.0ml, 47 mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (27.4 mg, 29.9 μmol) and Xantphos(34.6 mg, 59.8 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (127 mg, 1.10 mmol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with 1.0 Mhydrochloric acid and ethyl acetate. The aqueous phase was extractedwith ethyl acetate. The combined organic phases were washed with water,brine and dried over sodium sulfate and concentrated under reducedpressure. The crude product was suspended in acetonitrile, thecrystalline material was collect by filtration and dried to yield 280 mg(62%) of the desired product.

LC-MS (method 10): R_(t)=1.73 min; MS (ESIpos): m/z=427 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.082 (14.13), 2.469(10.11), 2.891 (11.15), 2.907 (0.98), 3.377 (1.43), 3.571 (1.01), 7.895(16.00), 8.553 (0.72), 9.653 (1.19).

Example 338(±)-4-{5-[(6-{4-[1-methoxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-yl)amino]-1,4-dimethyl-1H-pyrazol-3-yl}benzonitrile

A solution of4-(5-{[6-(4-acetyl-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-1,4-dimethyl-1H-pyrazol-3-yl)benzonitrile(200 mg, 469 μmol) in methanol (8.3 ml, 210 mmol) was treated withsodium borohydride (8.87 mg, 234 μmol) and stirred 2 hours at roomtemperature. Conversion to the alcohol was observed. Some dropshydrochloric acid were added and the mixture was stirred overnight. Themixture was purified by preparative HPLC (method: column: Reprosil C18;10 μm; 125×30 mm/flow: 50 mL/min/solvent: A=water (0.01% formic acid),B=acetonitrile/grradient: 0.00-5.00 min=10% B, 6.50 min=20% B,17.0-19.75 min=100% B, 19.75-23.00 min=90% B) to yield 71.1 mg (34%) ofthe desired product.

LC-MS (method 9): R_(t)=1.06 min; MS (ESIpos): m/z=443 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.19), 0.008(1.18), 1.356 (4.54), 1.373 (4.59), 2.072 (13.08), 2.210 (3.28), 2.636(13.65), 3.096 (11.84), 3.694 (9.23), 4.389 (1.37), 4.406 (1.34), 4.422(0.40), 7.896 (16.00), 8.474 (0.79), 9.464 (2.05).

Example 3394-{5-[(6-{4-[1-methoxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-yl)amino]-1,4-dimethyl-1H-pyrazol-3-yl}benzonitrile

A sample of racemic4-{5-[(6-{4-[1-methoxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-yl)amino]-1,4-dimethyl-1H-pyrazol-3-yl}benzonitrile(58 mg, 0.13 mmol) was separated using preparative SFC (column: 250*20mm AD-H, 5 μM, flow 80 mL/min, 40° C., solvent 85% carbon dioxide/15%methanol) to give 17.1 mg of the first eluting enantiomer of4-{5-[(6-{4-[1-methoxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-yl)amino]-1,4-dimethyl-1H-pyrazol-3-yl}benzonitrile(29% yield from racemate).

LC-MS (method 9): R_(t)=1.06 min; MS (ESIpos): m/z=443 [M+H]⁺

Chiral HPLC (SFC, Daicel A, 5 μM, flow 3 mL/min, solvent: 85% carbondioxide/15% iso-propanol) Rt=3.0 min, >99.5% enantiomeric excess.

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.357 (4.31), 1.373(4.36), 2.073 (12.69), 2.211 (3.21), 2.636 (13.48), 3.097 (11.65), 3.695(9.08), 4.390 (1.30), 4.407 (1.29), 7.897 (16.00), 8.476 (0.90), 9.465(1.99).

Example 3404-{5-[(6-{4-[1-methoxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-yl)amino]-1,4-dimethyl-1H-pyrazol-3-yl}benzonitrile

A sample of racemic4-{5-[(6-{4-[1-methoxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-yl)amino]-1,4-dimethyl-1H-pyrazol-3-yl}benzonitrile(58 mg, 0.13 mmol) was separated using preparative SFC (column: 250*20mm AD-H, 5 μM, flow 80 mL/min, 40° C., solvent 85% carbon dioxide/15%methanol) to give 16.7 mg of the second eluting enantiomer of4-{5-[(6-{4-[1-methoxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-yl)amino]-1,4-dimethyl-1H-pyrazol-3-yl}benzonitrile(29% yield from racemate).

LC-MS (method 9): R_(t)=1.06 min; MS (ESIpos): m/z=443 [M+H]⁺

Chiral HPLC (SFC, Daicel AD, 5 μM, flow 3 mL/min, solvent: 85% carbondioxide/15% iso-propanol) Rt=3.6 min, >99.5% enantiomeric excess.

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.357 (4.32), 1.373(4.35), 2.073 (12.85), 2.210 (3.08), 2.636 (13.65), 3.097 (11.71), 3.696(9.03), 4.390 (1.31), 4.406 (1.29), 7.897 (16.00), 8.475 (0.83), 9.465(1.94).

Example 341(±)-4-{1-(cyclopropylmethyl)-5-[(6-{4-[1-hydroxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-yl)amino]-4-methyl-1H-pyrazol-3-yl}benzonitrile(racemate)

A solution of4-[5-{[6-(4-acetyl-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(293 mg, 628 μmol) in methanol was treated with sodium borohydride (11.9mg, 314 μmol) and stirred 39 minutes at ambient temperature. Completeconversion to the alcohol was observed. Some drops of hydrochloric acidwere added and the mixture was left overnight. The mixture was dilutedwith water and extracted with ethyl acetate. The organic phases weredried over Extrelut NT3. The crude product was purified byflash-chromatography (column: Biotage SNAP KP-Sil 10 g, solvent: 90%dichloromethane/10% ethyl acetate to 88% dichloromethane/12%ethylacetate to 100% ethyl acetate) to yield 81.6 mg (28%) of thedesired product.

LC-MS (method 10): R_(t)=1.81 min; MS (ESIpos): m/z=469 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.305 (2.36), 0.316(2.61), 0.431 (2.29), 0.451 (2.41), 1.073 (1.11), 1.091 (2.29), 1.109(1.14), 1.177 (0.39), 1.189 (0.65), 1.207 (0.97), 1.226 (0.64), 1.322(4.85), 1.338 (4.90), 1.365 (0.53), 2.059 (14.27), 2.238 (2.98), 2.314(1.02), 2.367 (0.19), 2.632 (16.00), 2.670 (0.24), 2.696 (0.99), 2.710(0.20), 3.357 (0.47), 3.375 (1.15), 3.392 (1.14), 3.409 (0.38), 3.859(2.31), 3.877 (2.26), 4.771 (1.04), 4.787 (1.07), 4.914 (0.99), 7.885(0.79), 7.906 (11.26), 7.931 (0.84), 8.451 (0.83), 9.395 (0.87).

Example 342(±)-4-{1-(cyclopropylmethyl)-5-[(6-{4-[1-ethoxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-yl)amino]-4-methyl-1H-pyrazol-3-yl}benzonitrile

A sample of racemic4-{1-(cyclopropylmethyl)-5-[(6-{4-[1-hydroxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-yl)amino]-4-methyl-1H-pyrazol-3-yl}benzonitrile(62 mg, 132 μmol) were submitted for chiral separation (column: 250*20mm Daicel Chiralcel OJ-H—, 5 μM, flow 15 mL/min, 70° C., solvent 85%n-heptane/15% ethanol). Instead of the desired enantiomers 24.0 mg ofthe described product were obtained.

LC-MS (method 9): R_(t)=1.23 min; MS (ESIpos): m/z=497 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.306 (2.70), 0.317(2.92), 0.434 (2.62), 0.453 (2.78), 1.062 (3.39), 1.079 (6.92), 1.097(3.51), 1.178 (0.46), 1.190 (0.75), 1.196 (0.73), 1.208 (1.09), 1.220(0.71), 1.227 (0.73), 1.346 (5.06), 1.363 (5.09), 2.062 (14.99), 2.211(3.16), 2.632 (16.00), 3.206 (0.59), 3.227 (1.16), 3.245 (1.37), 3.263(1.48), 3.280 (1.31), 3.861 (2.43), 3.878 (2.37), 4.472 (0.48), 4.488(1.42), 4.505 (1.41), 4.521 (0.46), 7.886 (1.00), 7.907 (11.28), 7.933(0.88), 8.461 (0.85), 9.422 (0.93).

Example 343(±)-N-[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]-6-{4-[1-methoxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-amine(racemate)

A solution of1-[1-(6-{[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]ethanone(130 mg, 310 μmol) in methanol (5.5 ml, 140 mmol) was treated withsodium borohydride (5.86 mg, 155 μmol) and stirred 2 hours at roomtemperature. Complete conversion to the alcohol was observed. Some dropshydrochloric acid were added and the mixture was left overnight. Themixture was purified using preparative HPLC (method: column: ReprosilC18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent: A=water (0.01% formicacid), B=acetonitrile/grradient: 0.00-5.00 min=10% B, 6.50 min=20% B,17.0-19.75 min=100% B, 19.75-23.00 min=90% B) to yield 60.1 mg (45%) ofthe desired product.

LC-MS (method 9): R_(t)=1.11 min; MS (ESIpos): m/z=436 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.361 (6.20), 1.378(6.26), 1.852 (11.72), 2.216 (12.59), 2.622 (13.08), 2.635 (0.57), 3.101(16.00), 3.686 (13.52), 4.371 (0.47), 4.388 (1.70), 4.404 (1.69), 4.421(0.47), 7.357 (1.74), 7.379 (4.49), 7.402 (2.19), 7.510 (2.10), 7.523(2.35), 7.531 (1.96), 7.545 (1.61), 8.454 (3.28), 9.399 (2.54).

Example 344N-[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]-6-{4-[1-methoxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-amine

A sample of racemicN-[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]-6-{4-[1-methoxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-amine(42 mg, 0.10 mmol) was separated using preparative SFC (column: 250*20mm AD-H, 5 μM, flow 80 mL/min, 40° C., solvent 72% carbon dioxide/28%methanol) to give 13.4 mg of the first eluting enantiomer ofN-[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]-6-{4-[1-methoxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-amine(32% yield from racemate).

LC-MS (method 9): R_(t)=1.11 min; MS (ESIpos): m/z=436 [M+H]⁺

Chiral HPLC (SFC, Daicel AD, 5 μM, flow 3 mL/min, solvent: 70% carbondioxide/30% iso-propanol) Rt=1.79 min, >99.5% enantiomeric excess.

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.361 (5.75), 1.378(5.80), 1.852 (10.71), 2.216 (11.87), 2.622 (12.42), 3.101 (16.00),3.686 (12.80), 4.371 (0.44), 4.388 (1.64), 4.404 (1.60), 4.421 (0.43),7.357 (1.67), 7.363 (0.81), 7.374 (2.13), 7.379 (4.21), 7.396 (0.71),7.402 (2.10), 7.509 (2.01), 7.515 (0.85), 7.523 (2.22), 7.531 (1.76),7.540 (0.68), 7.545 (1.51), 8.454 (2.74), 9.397 (2.23).

Example 345N-[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]-6-{4-[1-methoxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-amine

A sample of racemicN-[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]-6-{4-[1-methoxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-amine(42 mg, 0.10 mmol) was separated using preparative SFC (column: 250*20mm AD-H, 5 μM, flow 80 mL/min, 40° C., solvent 72% carbon dioxide/28%methanol) to give 15.8 mg of the second eluting enantiomer ofN-[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]-6-{4-[1-methoxyethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-amine(38% yield from racemate).

LC-MS (method 9): R_(t)=1.11 min; MS (ESIpos): m/z=436 [M+H]⁺

Chiral HPLC (SFC, Daicel AD, 5 μM, flow 3 mL/min, solvent: 70% carbondioxide/30% iso-propanol) Rt=2.63 min, >99.5% enantiomeric excess

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.245 (0.69), 1.361(5.72), 1.378 (5.74), 1.852 (10.82), 2.216 (11.78), 2.623 (12.26), 3.102(16.00), 3.686 (12.95), 3.836 (1.29), 4.371 (0.43), 4.388 (1.60), 4.404(1.57), 4.421 (0.43), 4.943 (0.76), 7.357 (1.65), 7.363 (0.80), 7.374(2.15), 7.379 (4.26), 7.396 (0.73), 7.402 (2.10), 7.510 (2.00), 7.515(0.85), 7.523 (2.22), 7.531 (1.78), 7.540 (0.68), 7.545 (1.52), 8.454(2.95), 9.397 (2.21).

Example 346N-[4-chloro-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-amine

A microwave vial was charged4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (100mg, 409 μmol) and4-chloro-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (101 mg, 450μmol) and the contents were suspended in 1,4-dioxane (2.0 ml). Thereaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (11.2 mg, 12.3 μmol) and Xantphos(14.2 mg, 24.5 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (52.2 mg, 450 μmol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with hydrochloricacid and extracted with ethyl acetate (2×). The combined organic phaseswere dried over Extrelut NT3 and concentrated under reduced pressure.The crude product was recrystallized from acetonitrile to yield 106.8 mg(59.5%) of the desired product.

LC-MS (method 10): R_(t)=2.27 min; MS (ESIpos): m/z=434 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.300 (13.49), 3.317(16.00), 3.569 (0.57), 6.783 (3.96), 7.299 (4.34), 7.413 (1.82), 7.435(4.02), 7.457 (2.30), 7.636 (2.28), 7.650 (2.59), 7.657 (2.40), 7.671(1.96), 7.688 (1.21), 7.824 (2.39), 7.960 (1.05), 8.505 (3.71), 9.742(3.05).

Example 3472-[1-(6-{[3-(4-chlorophenyl)-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]propan-2-ol

A solution of ethyl1-(6-{[3-(4-chlorophenyl)-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(136 mg, 269 μmol) in tetrahydrofuran (2.7 ml, 34 mmol) was treated at0° C. with chloro(methyl)magnesium (310 μl, 3.0 M, 940 μmol). Themixture was stirred overnight at ambient temperature. The mixture wasdiluted with potassium sodium tartrate solution and water, and extractedwith ethyl acetate (3×). The combined organic phases were dried overExtrelut NT3 and concentrated under reduced pressure. The crude productwas purified by preparative HPLC (method: column: Reprosil C18; 10 μm;125×40 mm/flow: 75 mL/min/solvent: A=water (0.1% formic acid),B=acetonitrile/grradient: 0.00-5.50 min=10% B, 17.65-19.48 min=95% B,19.66 min=10% B) to yield 20 mg (15%) of the desired product.

LC-MS (method 10): R_(t)=2.14 min; MS (ESIpos): m/z=492 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.294 (2.08), 0.305(2.24), 0.424 (1.98), 0.444 (2.08), 1.091 (0.81), 1.108 (0.40), 1.180(0.60), 1.186 (0.57), 1.198 (0.82), 1.216 (0.52), 1.356 (0.43), 1.464(16.00), 2.014 (11.59), 2.265 (2.55), 2.742 (11.76), 3.375 (0.43), 3.392(0.40), 3.831 (1.97), 3.848 (1.95), 4.854 (3.36), 7.488 (3.28), 7.509(4.15), 7.713 (3.07), 7.734 (2.66), 8.458 (0.62), 9.373 (0.70).

Example 3481-(6-{[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbonitrile

A microwave vial was charged1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbonitrile (175mg, 77% purity, 576 μmol),5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-amine (130 mg, 633 μmol)and sodium phenolate (73.5 mg, 633 μmol) and the contents were suspendedin 1,4-dioxane (3.3 ml, 39 mmol). The reaction mixture was degassed withAr for 3 min. Tris(dibenzylidenaceton)dipalladium (6.85 mg, 7.49 μmol)and Xantphos (10.0 mg, 17.3 μmol) were added and the reaction mixturewas degassed again for 1 min. The vial was sealed and heated at 85° C.overnight while vigorously stirring. After cooling to ambienttemperature, the reaction mixture was filtered and purified bypreparative HPLC (method 3) to yield the desired product (70.0 mg, 30%).

LC-MS (method 10): R_(t)=2.04 min; MS (ESIpos): m/z=403 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.855 (11.25), 2.339(14.01), 2.786 (15.03), 3.688 (16.00), 7.358 (1.83), 7.380 (4.10), 7.402(2.45), 7.464 (0.71), 7.510 (2.51), 7.524 (2.82), 7.531 (2.32), 7.545(1.90), 8.536 (2.86), 9.662 (1.56).

Example 3491-(6-{[1-(cyclopropylmethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbonitrile

A microwave vial was charged1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbonitrile (138mg, 77% purity, 456 μmol),1-(cyclopropylmethyl)-4-ethyl-3-(4-fluorophenyl)-1H-pyrazol-5-amine (130mg, 501 μmol) and sodium phenolate (58.2 mg, 501 μmol) and the contentswere suspended in 1,4-dioxane (2.6 ml, 31 mmol). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylidenaceton)dipalladium(5.43 mg, 5.92 μmol) and Xantphos (7.91 mg, 13.7 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously stirring. After coolingto ambient temperature, the reaction mixture was filtered and purifiedby preparative HPLC (method 4) to yield the desired product (56.0 mg,26%).

LC-MS (method 10): R_(t)=2.29 min; MS (ESIpos): m/z=457 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.006 (1.45), 0.006(0.82), 0.295 (2.10), 0.435 (2.59), 0.450 (2.60), 0.972 (4.15), 0.987(8.51), 1.002 (4.12), 1.078 (1.10), 1.092 (2.20), 1.106 (1.11), 1.195(1.10), 2.347 (1.30), 2.359 (1.21), 2.363 (1.21), 2.404 (1.87), 2.456(1.83), 2.471 (1.95), 2.796 (16.00), 2.870 (1.65), 3.391 (1.75), 3.405(0.62), 3.799 (1.77), 7.259 (2.13), 7.276 (4.29), 7.294 (2.43), 7.686(1.82).

Example 350N-[1-(cyclopropylmethyl)-4-methyl-3-(pyridin-4-yl)-1H-pyrazol-5-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged with1-(cyclopropylmethyl)-4-methyl-3-(pyridin-4-yl)-1H-pyrazol-5-amine (79.0mg, 346 μmol), 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (79.4mg, 381 μmol) and sodium phenolate (44.2 mg, 381 μmol) and the contentswere suspended in 1,4-dioxane (1.3 mL). The reaction mixture wasdegassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (6.34mg, 6.92 μmol) and XantPhos (8.01 mg, 13.8 μmol) were added and thereaction mixture was degassed again for 1 min. The vial was sealed andheated at 85° C. overnight while vigorously shaking. After cooling toambient temperature, the reaction mixture was filtered and concentrated.The residue was redissolved in dimethylsulfoxide and purified bypreparative HPLC (Instrument: Waters Prep LC/MS System, Column: XBridgeC18 5 μm 100×30 mm; Solvent A: water, solvent B: acetonitrile, flow: 65mL/min plus 5 ml 2% aqueous ammonia solution, room temperature,wavelength 200-400 nm, At-column injection; gradient: 0-2 min 10%solvent B, 2-2.2 min to 30% solvent B, 2.2-7 min to 70% solvent B, 7-7.5min to 92% solvent B, 7.5-9 min at 92% B) to yield the desired product(32.8 mg, 23% yield).

LC-MS (method 11): R_(t)=1.02 min; MS (ESIneg): m/z=399 [M−H]⁻

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.30), −0.008(2.63), 0.008 (2.41), 0.146 (0.27), 0.308 (2.49), 0.319 (2.76), 0.433(2.53), 0.453 (2.68), 1.179 (0.35), 1.191 (0.65), 1.198 (0.65), 1.211(1.02), 1.222 (0.63), 1.230 (0.64), 2.081 (16.00), 2.172 (3.25), 2.228(2.24), 2.328 (0.52), 2.367 (0.29), 2.523 (1.36), 2.630 (14.92), 2.665(2.01), 2.710 (0.32), 3.866 (2.50), 3.884 (2.48), 6.146 (2.69), 6.271(0.32), 7.694 (3.29), 7.709 (3.54), 7.900 (0.35), 8.464 (0.66), 8.608(4.65), 8.612 (3.20), 8.620 (3.06), 8.623 (4.69), 8.903 (0.28), 9.419(0.90).

Example 3516-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-[1-(cyclopropylmethyl)-4-methyl-3-(pyridin-4-yl)-1H-pyrazol-5-yl]pyrimidin-4-amine

A microwave vial was charged with1-(cyclopropylmethyl)-4-methyl-3-(pyridin-4-yl)-1H-pyrazol-5-amine (200mg, 876 μmol),4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (234 mg,964 μmol) and sodium phenolate (112 mg, 964 μmol) and the contents weresuspended in 1,4-dioxane (2.5 mL). The reaction mixture was degassedwith Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (16.0 mg, 17.5μmol) and XantPhos (20.3 mg, 35.0 μmol) were added and the reactionmixture was degassed again for 1 min. The vial was sealed and heated at85° C. overnight while vigorously shaking. After cooling to ambienttemperature, the reaction mixture was quenched with aqueous sodiumhydrogencarbonate solution and extracted with ethyl acetate. The organicphase extract was washed with brine, dried over sodium sulfate andconcentrated. The residue was purified by flash column chromatography(SNAP Ultra 25 g, cyclohexane/ethyl acetate gradient 88/12 to 0/100) toyield the desired product (112 mg, 29% yield).

LC-MS (method 11): R_(t)=1.30 min; MS (ESIpos): m/z=435 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.18), 0.008(1.37), 0.306 (2.17), 0.317 (2.41), 0.433 (2.23), 0.453 (2.39), 1.188(0.60), 1.195 (0.58), 1.207 (0.91), 1.219 (0.55), 1.226 (0.59), 2.079(13.98), 2.212 (2.33), 2.649 (16.00), 2.670 (0.45), 3.867 (2.11), 3.884(2.07), 7.693 (2.77), 7.707 (2.91), 8.500 (0.44), 8.609 (3.88), 8.624(3.87), 9.518 (0.47).

Example 3521-(6-{[3-(4-cyanophenyl)-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbonitrile

A microwave vial was charged1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbonitrile (142mg, 77% purity, 468 μmol),4-[5-amino-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(130 mg, 515 μmol) and sodium phenolate (59.8 mg, 515 μmol) and thecontents were suspended in 1,4-dioxane (2.7 ml, 32 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (5.58 mg, 6.09 μmol) and Xantphos(8.13 mg, 14.1 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was filtered and purified by preparative HPLC (method4) and an additional preparative HPLC (method: column: Reprosil C18; 10μm; 125×40 mm/flow: 75 mL/min/solvent: A=water (0.1% formic acid),B=acetonitrile/gradient: 0.00-5.50 min=10% B, 17.65-19.48 min=95% B,19.66 min=10% B) to yield the desired product (37.0 mg, 17%).

LC-MS (method 10): R_(t)=2.14 min; MS (ESIpos): m/z=450 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.35), 0.008(1.27), 0.302 (2.33), 0.313 (2.53), 0.432 (2.45), 0.452 (2.61), 1.074(1.29), 1.091 (2.62), 1.109 (1.32), 1.184 (0.68), 1.191 (0.67), 1.203(1.01), 1.215 (0.62), 1.221 (0.65), 2.060 (15.39), 2.329 (2.02), 2.796(16.00), 3.357 (0.78), 3.375 (1.43), 3.393 (1.35), 3.410 (0.47), 3.862(1.96), 3.879 (1.96), 7.908 (12.65).

Example 353 ethyl1-(6-{[5-(4-chlorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

A microwave vial was charged ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (161mg, 574 μmol), 5-(4-chlorophenyl)-1,4-dimethyl-1H-pyrazol-3-amine (140mg, 632 μmol) and sodium phenolate (73.3 mg, 632 μmol) and the contentswere suspended in 1,4-dioxane (3.3 ml, 39 mmol). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylidenaceton)dipalladium(6.83 mg, 7.46 μmol) and Xantphos (9.97 mg, 17.2 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously stirring. After coolingto ambient temperature, the reaction mixture was filtered and purifiedby preparative HPLC (method 4) to yield the desired product (138 mg,49%).

LC-MS (method 10): R_(t)=2.41 min; MS (ESIpos): m/z=466 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.290 (4.44), 1.308(9.24), 1.326 (4.65), 1.868 (12.80), 2.030 (0.78), 2.382 (14.96), 2.889(15.62), 2.910 (0.79), 2.933 (0.62), 3.672 (0.53), 3.699 (16.00), 4.230(1.37), 4.248 (4.25), 4.265 (4.23), 4.283 (1.38), 7.426 (1.09), 7.495(3.74), 7.516 (5.58), 7.596 (5.28), 7.617 (3.59), 8.529 (3.17), 9.607(2.25).

Example 354

N-[3-(4-chlorophenyl)-1,4-dimethyl-1H-pyrazol-5-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (128 mg, 615 μmol),3-(4-chlorophenyl)-1,4-dimethyl-1H-pyrazol-5-amine (150 mg, 677 μmol)and sodium phenolate (78.5 mg, 677 μmol) and the contents were suspendedin 1,4-dioxane (3.5 ml, 41 mmol). The reaction mixture was degassed withAr for 3 min. Tris(dibenzylidenaceton)dipalladium (7.32 mg, 8.00 μmol)and Xantphos (10.7 mg, 18.5 μmol) were added and the reaction mixturewas degassed again for 1 min. The vial was sealed and heated at 85° C.overnight while vigorously stirring. After cooling to ambienttemperature, the reaction mixture was filtered and purified bypreparative HPLC (method 4) to yield the desired product (117 mg, 46%).

LC-MS (method 10): R_(t)=2.19 min; MS (ESIpos): m/z=394 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.90), 0.008(0.98), 2.027 (16.00), 2.074 (0.47), 2.174 (4.26), 2.630 (14.11), 3.666(11.41), 6.145 (2.95), 7.483 (3.96), 7.504 (4.80), 7.703 (3.75), 7.724(3.09), 8.470 (0.91), 9.419 (2.37).

Example 355N-[5-(4-chlorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (89.8 mg, 431 μmol),5-(4-chlorophenyl)-1,4-dimethyl-1H-pyrazol-3-amine (105 mg, 474 μmol)and sodium phenolate (55.0 mg, 474 μmol) and the contents were suspendedin 1,4-dioxane (2.5 ml, 29 mmol). The reaction mixture was degassed withAr for 3 min. Tris(dibenzylidenaceton)dipalladium (5.13 mg, 5.60 μmol)and Xantphos (7.47 mg, 12.9 μmol) were added and the reaction mixturewas degassed again for 1 min. The vial was sealed and heated at 85° C.overnight while vigorously stirring. After cooling to ambienttemperature, the reaction mixture was diluted with hydrochlorid acid andextracted with ethyl acetate (2×). The combined organic phases weredried over Extrelut NT3 and concentrated under reduced pressure. Thecrude product was purified by preparative HPLC (method 4) to yield thedesired product (20.0 mg, 11%).

LC-MS (method 10): R_(t)=2.19 min; MS (ESIpos): m/z=394 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.48), 0.008(1.58), 1.566 (0.75), 1.646 (0.76), 1.859 (13.87), 2.027 (1.99), 2.073(0.52), 2.184 (14.80), 2.328 (0.47), 2.622 (13.05), 2.653 (0.53), 2.670(0.55), 3.666 (1.39), 3.702 (16.00), 6.131 (3.70), 6.147 (0.44), 7.341(0.51), 7.370 (2.53), 7.382 (1.21), 7.398 (0.82), 7.461 (0.78), 7.465(0.89), 7.484 (0.85), 7.496 (3.87), 7.517 (5.68), 7.596 (5.67), 7.617(3.71), 7.702 (0.51), 7.724 (0.48), 7.781 (0.46), 7.794 (0.44), 7.821(0.40), 8.447 (3.63), 9.389 (2.95).

Example 356 ethyl1-(6-{[4-chloro-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

4-chloro-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (200 mg, 886μmol) and sodium phenolate (103 mg, 886 μmol) and were suspended in1,4-dioxane (1.9 mL). The reaction mixture was degassed with Ar for 3min. Tris(dibenzylideneacetone)dipalladium (9.59 mg, 10.5 μmol),XantPhos (14.0 mg, 24.2 μmol) and ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (226mg, 806 μmol) were added and the reaction mixture was degassed again for1 min. the reaction mixture was heated at 90° C. overnight whilevigorously stirring. After cooling to ambient temperature, the reactionmixture was filtered and concentrated. The residue was purified by flashcolumn chromatography (SNAP Ultra 25g, cyclohexane/ethyl acetategradient 95/5 to 20/80) to yield the desired product (95 mg, 24% yield).

LC-MS (method 10): R_(t)=2.35 min; MS (ESIpos): m/z=470 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.30), 0.008(1.32), 1.157 (0.16), 1.175 (0.30), 1.274 (0.17), 1.291 (4.76), 1.309(10.08), 1.327 (4.84), 1.398 (1.96), 1.988 (0.46), 2.328 (0.25), 2.387(15.76), 2.670 (0.26), 2.899 (16.00), 2.919 (1.51), 2.946 (1.14), 3.733(1.04), 3.770 (15.97), 3.882 (0.53), 4.232 (1.31), 4.250 (4.21), 4.267(4.18), 4.278 (0.49), 4.285 (1.30), 7.301 (3.62), 7.324 (0.43), 7.346(0.23), 7.409 (2.00), 7.414 (0.74), 7.425 (0.92), 7.431 (4.41), 7.448(0.83), 7.453 (2.49), 7.466 (0.24), 7.628 (2.37), 7.633 (1.05), 7.642(2.60), 7.650 (2.28), 7.658 (0.88), 7.664 (2.00), 7.733 (0.37), 7.877(0.22), 7.890 (0.24), 7.899 (0.22), 7.912 (0.20), 8.553 (3.06), 8.580(0.18), 8.932 (0.29), 9.732 (2.56), 9.863 (0.21).

Example 3571-[1-(6-{[4-chloro-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]cyclopropanol

Under an argon atmosphere a Schlenk tube was charged with titaniumisopropoxide (310 μl, 1.0 mmol) in tetrahydrofuran (2.0 ml, 25 mmol) anda solution of ethylmagnesium bromide (3.1 ml, 1.0 M in tetrahydrofuran,3.1 mmol) was added at −18° C. The mixture was stirred at thistemperature for 30 minutes, than a solution of ethyl1-(6-{[4-chloro-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(245 mg, 521 μmol) in 1.5 mL tetrahydrofuran was added. The mixture wasstirred overnight at room temperature. No complete conversion wasobserved, therefor additional 2 equivalents of ethylmagnesium bromide(1.1 ml, 1.0 M in tetrahydrofuran, 1.1 mmol) were added. The mixture wasagain left overnight. The mixture was diluted with water and extractedwith ethyl acetate (3×). The combined organic phases were washed withwater, brine, dried over sodium sulfate and concentrated under reducedpressure. The crude product was purified by preparative HPLC (method 17)to yield 34.3 mg (14%) of the desired product.

LC-MS (method 9): R_(t)=0.95 min; MS (ESIpos): m/z=454 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.89), 0.008(0.91), 0.644 (1.13), 0.656 (3.45), 0.661 (3.41), 0.673 (1.37), 0.930(1.35), 0.941 (3.57), 0.947 (3.38), 0.959 (1.23), 2.281 (14.40), 2.524(0.62), 2.709 (15.11), 3.768 (16.00), 5.471 (5.44), 5.754 (3.58), 7.241(3.94), 7.243 (4.15), 7.408 (2.02), 7.413 (0.78), 7.430 (4.45), 7.447(0.88), 7.452 (2.54), 7.626 (2.46), 7.632 (1.13), 7.640 (2.68), 7.648(2.35), 7.657 (0.92), 7.662 (2.04), 8.472 (3.36), 9.520 (3.30).

Example 3584-{1-(cyclopropylmethyl)-5-[(6-{3,5-dimethyl-4-[(±)-2,2,2-trifluoro-1-hydroxyethyl]-1H-pyrazol-1-yl}pyrimidin-4-yl)amino]-4-methyl-1H-pyrazol-3-yl}benzonitrile(racemate)

Molecular Sieves (4 Å) were placed in a round-bottom flask and dried ina vacuum drying-oven overnight at 120° C. After cooling to ambienttemperature, tetrabutylammonium fluoride trihydrate (42.6 mg, 152 μmol)and toluene (1.0 mL) were added and the suspension stirred for 30 min. Asolution of4-[1-(cyclopropylmethyl)-5-{[6-(4-formyl-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-4-methyl-1H-pyrazol-3-yl]benzonitrile(23.0 mg, 50.8 μmol) in toluene (0.5 mL) was then added, the mixture wasstired for 5 min and cooled to 0° C. Trimethyl(trifluoromethyl)silane(38 μL, 250 μmol) was then added and stirred at ambient temperature for1 h. The reaction mixture was diluted with ethyl acetate and water, themolecular sieves removed by filtration and washed further with ethylacetate. After separation of the layers, the aqueous phase was extractedagain with ethyl acetate and the combined organic phase extracts weredried over sodium sulfate and concentrated. The residue was purified bypreparative HPLC (column: Chromatorex C18; 125*30 mm, 10 μM, flow 75mL/min, gradient acetonitrile/water 5/95 to 90/10) to yield the desiredproduct (8 mg, 85% purity, 26% yield).

LC-MS (method 11): R_(t)=1.39 min; MS (ESIneg): m/z=521 [M−H]⁻

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.65), −0.008(5.04), 0.008 (5.06), 0.146 (0.61), 0.306 (2.70), 0.317 (2.95), 0.433(2.64), 0.453 (2.78), 1.148 (0.16), 1.178 (0.40), 1.190 (0.71), 1.196(0.71), 1.209 (1.10), 1.228 (0.77), 2.025 (0.27), 2.062 (16.00), 2.242(2.57), 2.328 (0.87), 2.367 (0.49), 2.407 (0.25), 2.674 (14.99), 2.710(0.51), 2.943 (1.34), 3.861 (2.35), 3.878 (2.34), 5.157 (0.69), 6.699(1.56), 6.709 (1.57), 7.885 (1.08), 7.906 (12.20), 7.931 (0.88), 8.487(0.53), 9.478 (0.55), 10.017 (0.31).

Example 3594-{1-(cyclopropylmethyl)-5-[(6-{3,5-dimethyl-4-[2,2,2-trifluoro-1-hydroxyethyl]-1H-pyrazol-1-yl}pyrimidin-4-yl)amino]-4-methyl-1H-pyrazol-3-yl}benzonitrile

Obtained from separation of the enantiomers of a racemic sample of4-{1-(cyclopropylmethyl)-5-[(6-{3,5-dimethyl-4-[(±)-2,2,2-trifluoro-1-hydroxyethyl]-1H-pyrazol-1-yl}pyrimidin-4-yl)amino]-4-methyl-1H-pyrazol-3-yl}benzonitrile(racemate 12.0 mg dissolved in ethanol, 1.5 mL) by preparative HPLC(Chiralpak AD-H 5 μm, 250×30 mm, flow: 40 mL/min, isocratic:2-propanol/n-heptane 15/85) to yield the title compound as the firsteluting enantiomer (3.4 mg, 28% from racemate).

LC-MS (method 11): R_(t)=1.38 min; MS (ESIpos): m/z=523 [M+H]⁺

Chiral HPLC (Daicel IC-3 3 μm, 50×4.6 mm, isocratic i-hexane/2-propanol90/10): Rt=5.82 min, 90% ee

Example 3604-{1-(cyclopropylmethyl)-5-[(6-{3,5-dimethyl-4-[(1S)-2,2,2-trifluoro-1-hydroxyethyl]-1H-pyrazol-1-yl}pyrimidin-4-yl)amino]-4-methyl-1H-pyrazol-3-yl}benzonitrile

Obtained from separation of the enantiomers of a racemic sample of4-{1-(cyclopropylmethyl)-5-[(6-{3,5-dimethyl-4-[(±)-2,2,2-trifluoro-1-hydroxyethyl]-1H-pyrazol-1-yl}pyrimidin-4-yl)amino]-4-methyl-1H-pyrazol-3-yl}benzonitrile(racemate 12.0 mg dissolved in ethanol, 1.5 mL) by preparative HPLC(Chiralpak AD-H 5 μm, 250×30 mm, flow: 40 mL/min, isocratic:2-propanol/n-heptane 15/85) to yield the title compound as the secondeluting enantiomer (2.2 mg, 18% from racemate).

LC-MS (method 11): R_(t)=1.38 min; MS (ESIpos): m/z=523 [M+H]⁺

Chiral HPLC (Daicel IC-3 3 μm, 50×4.6 mm, isocratic i-hexane/2-propanol90/10): Rt=8.11 min, 99% ee

Example 361 ethyl1-[6-({1,4-dimethyl-3-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3,5-dimethyl-1H-pyrazole-4-carboxylate

1,4-dimethyl-3-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-5-amine (300 mg,1.11 mmol) and sodium phenolate (128 mg, 1.11 mmol) and the contentswere suspended in 1,4-dioxane (4.0 mL). The reaction mixture wasdegassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (12.0mg, 13.1 μmol), XantPhos (17.5 mg, 30.2 μmol) and ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (282mg, 1.01 mmol) were added and the reaction mixture was degassed againfor 1 min. The vial was sealed and heated at 90° C. overnight whilevigorously shaking. After cooling to ambient temperature, the reactionmixture loaded onto silica gel and purified by flash columnchromatography (SNAP Ultra 25 g, cyclohexane/ethyl acetate gradient 95/5to 35/65) to yield the desired product (119 mg, 23% yield).

LC-MS (method 9): R_(t)=1.30 min; MS (ESIpos): m/z=516 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.69), 0.008(1.71), 1.289 (3.67), 1.307 (7.55), 1.324 (3.76), 1.398 (1.52), 1.988(0.50), 2.043 (16.00), 2.328 (0.48), 2.378 (2.87), 2.912 (14.29), 3.680(9.39), 4.230 (1.08), 4.248 (3.32), 4.266 (3.29), 4.283 (1.09), 7.420(2.87), 7.440 (3.15), 7.800 (3.15), 7.821 (2.86), 8.550 (0.62), 9.603(1.04).

Example 362 ethyl1-[6-({1,4-dimethyl-3-[4-(trifluoromethyl)phenyl]-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3,5-dimethyl-1H-pyrazole-4-carboxylate

1,4-dimethyl-3-[4-(trifluoromethyl)phenyl]-1H-pyrazol-5-amine (223 mg,874 μmol) and sodium phenolate (101 mg, 874 μmol) were suspended in1,4-dioxane (3.2 mL). The reaction mixture was degassed with Ar for 3min. Tris(dibenzylideneacetone)dipalladium (9.46 mg, 10.3 μmol),XantPhos (13.8 mg, 23.8 μmol) and ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (223mg, 794 μmol) were added and the reaction mixture was degassed again for1 min. The reaction mixture was heated at 90° C. overnight whilevigorously stirring. After cooling to ambient temperature, the reactionmixture was loaded onto silica gel and purified by flash columnchromatography (SNAP Ultra 25 g, cyclohexane/ethyl acetate gradient 95/5to 35/65) to yield the desired product (175 mg, 44% yield).

LC-MS (method 9): R_(t)=1.28 min; MS (ESIpos): m/z=500 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.008 (0.83), 1.158(0.45), 1.176 (0.87), 1.194 (0.45), 1.290 (3.70), 1.308 (7.55), 1.326(3.77), 1.398 (2.19), 1.989 (1.52), 2.078 (16.00), 2.380 (2.99), 2.914(14.30), 3.704 (9.62), 4.231 (1.12), 4.249 (3.37), 4.267 (3.35), 4.285(1.15), 7.784 (2.97), 7.805 (4.05), 7.916 (3.30), 7.937 (2.46), 8.552(0.64), 9.629 (1.13).

Example 363 ethyl1-(6-{[3-(2,4-difluorophenyl)-1,4-dimethyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

3-(2,4-difluorophenyl)-1,4-dimethyl-1H-pyrazol-5-amine (300 mg, 1.34mmol) and sodium phenolate (156 mg, 1.34 mmol) were suspended in1,4-dioxane (4.9 mL). The reaction mixture was degassed with Ar for 3min. Tris(dibenzylideneacetone)dipalladium (14.5 mg, 15.9 μmol),XantPhos (21.2 mg, 36.7 μmol) and ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (343mg, 1.22 mmol) were added and the reaction mixture was degassed againfor 1 min. The reaction mixture was heated at 90° C. overnight whilevigorously stirring. After cooling to ambient temperature, the reactionmixture was loaded onto silica gel and purified by flash columnchromatography (SNAP Ultra 25 g, cyclohexane/ethyl acetate gradient 95/5to 35/65) to yield the desired product (263 mg, 46% yield).

LC-MS (method 9): R_(t)=1.18 min; MS (ESIpos): m/z=468 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.18), −0.008(1.60), 0.008 (1.47), 0.146 (0.17), 1.157 (0.80), 1.175 (1.58), 1.193(0.80), 1.291 (4.33), 1.309 (9.02), 1.327 (4.42), 1.824 (8.11), 1.828(8.35), 1.909 (0.29), 1.989 (2.84), 2.328 (0.34), 2.384 (5.22), 2.671(0.29), 2.915 (16.00), 3.679 (9.94), 4.003 (0.22), 4.021 (0.68), 4.039(0.69), 4.057 (0.22), 4.233 (1.28), 4.251 (3.95), 4.268 (3.94), 4.286(1.28), 7.153 (0.66), 7.160 (0.72), 7.175 (1.21), 7.180 (1.28), 7.194(0.76), 7.200 (0.82), 7.326 (0.72), 7.332 (0.73), 7.352 (1.24), 7.357(1.24), 7.376 (0.75), 7.382 (0.74), 7.540 (0.64), 7.561 (1.35), 7.579(1.32), 7.600 (0.61), 8.558 (1.09), 9.597 (0.91).

Example 364 ethyl1-(6-{[1-(cyclopropylmethyl)-3-(2,4-difluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

A microwave vial was charged with ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (275mg, 95% purity, 932 μmol),1-(cyclopropylmethyl)-3-(2,4-difluorophenyl)-4-methyl-1H-pyrazol-5-amine(300 mg, 90% purity, 1.03 mmol) and sodium phenolate (119 mg, 1.03 mmol)and the contents were suspended in 1,4-dioxane (3.0 mL). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (17.1 mg, 18.6 μmol) and XantPhos(21.6 mg, 37.3 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously shaking. After cooling to ambient temperature, thereaction mixture was filtered and concentrated. The residue wasredissolved in dimethylsulfoxide and purified by preparative HPLC(column: Chromatorex C18; 250*40 mm, 10 μM, flow 100 mL/min, gradientacetonitrile/water (containing 0.1% trifluoroacetic acid) 10/90 to 95/5)and further purified by flash column chromatography (SNAP Ultra 25 g,cyclohexane/ethyl acetate gradient) to yield the desired product (117mg, 23% yield).

LC-MS (method 11): R_(t)=1.58 min; MS (ESIpos): m/z=508 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.33), −0.008(2.67), 0.008 (2.03), 0.146 (0.29), 0.279 (0.69), 0.291 (2.86), 0.304(3.12), 0.316 (0.87), 0.429 (2.63), 0.449 (2.79), 1.149 (0.23), 1.168(0.40), 1.180 (0.72), 1.187 (0.69), 1.199 (1.07), 1.211 (0.67), 1.218(0.68), 1.231 (0.49), 1.290 (4.66), 1.308 (9.61), 1.326 (4.74), 1.398(11.27), 1.819 (9.11), 1.824 (9.09), 2.328 (0.48), 2.333 (0.42), 2.379(4.01), 2.419 (0.42), 2.671 (0.40), 2.711 (0.22), 2.915 (16.00), 2.951(0.27), 3.575 (0.18), 3.592 (0.39), 3.608 (0.18), 3.847 (2.43), 3.864(2.42), 4.231 (1.35), 4.249 (4.22), 4.267 (4.23), 4.284 (1.41), 7.160(0.69), 7.167 (0.76), 7.181 (1.39), 7.187 (1.50), 7.202 (0.86), 7.208(0.92), 7.329 (0.74), 7.335 (0.76), 7.359 (1.27), 7.379 (0.79), 7.385(0.79), 7.558 (0.60), 7.580 (1.33), 7.597 (1.29), 7.618 (0.61), 8.548(0.73), 9.545 (0.36).

Example 3654-[1-(cyclopropylmethyl)-4-methyl-5-{[6-(3-methyl-4-oxo-5,6-dihydrocyclopenta[c]pyrazol-1(4H)-yl)pyrimidin-4-yl]amino}-1H-pyrazol-3-yl]benzonitrile

1-(6-chloropyrimidin-4-yl)-3-methyl-5,6-dihydrocyclopenta[c]pyrazol-4(1H)-one(500 mg, 2.01 mmol) and sodium phenolate (257 mg, 2.21 mmol) weresuspended in 1,4-dioxane (X mL). The reaction mixture was degassed withAr for 3 min. Tris(dibenzylideneacetone)dipalladium (34.9 mg, 60.3μmol), XantPhos (27.6 mg, 30.2 μmol) and4-[5-amino-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(558 mg, 2.21 mmol) were added and the reaction mixture was degassedagain for 1 min. The reaction mixture was heated at 90° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with water and extracted with ethyl acetate(3×). The combined organic phase extracts were dried over sodium sulfateand concentrated. The residue was dissolved in dimethylsulfoxide (20 mL)purified by preparative HPLC (Kinetex C18 5 μm, 150×30 mm;water/acetonitrile gradient 65/35 to 5/95; flow: 75 mL/min, 500 μLinjections every 10 min) to yield the desired product (230 mg, 22%yield).

LC-MS (method 9): R_(t)=1.03 min; MS (ESIpos): m/z=465 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.120 (0.23), −0.007(2.52), 0.007 (1.77), 0.117 (0.23), 0.305 (2.41), 0.313 (2.45), 0.435(2.81), 0.451 (2.83), 1.182 (0.47), 1.191 (0.85), 1.197 (0.84), 1.206(1.25), 1.216 (0.78), 1.221 (0.78), 1.231 (0.40), 2.070 (16.00), 2.074(7.68), 2.306 (1.28), 2.359 (0.59), 2.363 (0.65), 2.366 (0.49), 2.520(0.72), 2.523 (0.54), 2.633 (0.29), 2.636 (0.40), 2.640 (0.29), 2.813(1.23), 2.939 (2.27), 2.948 (2.66), 2.954 (2.40), 2.958 (2.32), 3.165(0.23), 3.175 (0.25), 3.339 (3.05), 3.344 (2.76), 3.350 (2.98), 3.354(2.63), 3.359 (2.58), 3.874 (1.76), 7.910 (7.53), 8.518 (0.28), 9.608(0.27).

Example 3664-[4-({6-[4-(2-hydroxypropan-2-yl)-3,5-dimethyl-1H-pyrazol-1-yl]pyrimidin-4-yl}amino)-3,5-dimethyl-1H-pyrazol-1-yl]benzonitrile

A solution of ethyl1-(6-{[1-(4-cyanophenyl)-3,5-dimethyl-1H-pyrazol-4-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(193 mg, 423 μmol) in tetrahydrofuran (8.3 ml, 100 mmol) was treated at0° C. with chloro(methyl)magnesium (490 3.0 M, 1.5 mmol) and stirredovernight at ambient temperature. The mixture was diluted with potassiumsodium tartrate solution and water and extracted with ethyl acetate(3×). The combined organic phases were dried over Extrelut NT3 andconcentrated under reduced pressure. The crude product was purified bypreparative HPLC (method: column: Reprosil C18; 10 μm; 125×40 mm/flow:75 mL/min/solvent: A=water (0.1% formic acid), B=acetonitrile/gradient:0.00-5.50 min=10% B, 17.65-19.48 min=95% B, 19.66 min=10% B) and(method 1) to yield 7.00 mg (4%) of the desired product.

LC-MS (method 10): R_(t)=1.54 min; MS (ESIpos): m/z=443 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.464 (16.00), 2.105(15.42), 2.263 (2.37), 2.289 (14.61), 2.328 (0.49), 2.720 (12.21), 4.838(2.69), 7.804 (2.54), 7.825 (3.16), 7.975 (4.37), 7.997 (3.46), 8.399(0.59), 8.933 (2.72).

Example 367 ethyl1-(6-{[3-(4-chlorophenyl)-1,4-dimethyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

A microwave vial was charged ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (288mg, 1.03 mmol), 3-(4-chlorophenyl)-1,4-dimethyl-1H-pyrazol-5-amine (250mg, 1.13 mmol) and sodium phenolate (131 mg, 1.13 mmol) and the contentswere suspended in 1,4-dioxane (5.0 ml, 58 mmol). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylidenaceton)dipalladium(12.2 mg, 13.3 μmol) and Xantphos (17.8 mg, 30.8 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously stirring. After coolingto ambient temperature, the reaction mixture was filtered and purifiedby preparative HPLC (method 4) and (method: column: Reprosil C18; 10 μm;125×40 mm/flow: 75 mL/min/solvent: A=water (0.1% formic acid),B=acetonitrile/grradient: 0.00-5.50 min=10% B, 17.65-19.48 min=95% B,19.66 min=10% B) to yield the desired product (190 mg, 40%).

LC-MS (method 9): R_(t)=1.26 min; MS (ESIpos): m/z=466 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.40), 1.074(0.64), 1.091 (1.32), 1.109 (0.66), 1.289 (3.60), 1.306 (7.46), 1.324(3.69), 2.030 (16.00), 2.377 (2.71), 2.524 (0.40), 2.910 (13.93), 3.375(0.69), 3.392 (0.66), 3.672 (8.98), 4.230 (1.08), 4.248 (3.28), 4.265(3.24), 4.283 (1.04), 7.483 (3.85), 7.504 (4.80), 7.699 (3.48), 7.720(2.89), 8.545 (0.50), 9.597 (0.96).

Example 3682-[1-(6-{[1-(cyclopropylmethyl)-3-(2,4-difluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]propan-2-ol

Under an argon atmosphere, ethyl1-(6-{[1-(cyclopropylmethyl)-3-(2,4-difluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(80.0 mg, 158 μmol) was dissolved in tetrahydrofuran and the solutioncooled to 0° C. A solution of bromo(methyl)magnesium (790 pi, 1.0 M, 790μmol) was added dropwise and the reaction mixture was stirred overnightat ambient temperature. The reaction mixture was carefully quenched byaddition of aqueous Na₂EDTA solution (10%) and extracted with ethylacetate. The organic phase extract was dried over sodium sulfate andconcentrated. The residue was purified by flash column chromatography(SNAP Ultra 10 g, cyclohexane/ethyl acetate gradient 95/5 to 5/95) toyield the desired product (6 mg, 7% yield).

LC-MS (method 11): R_(t)=1.38 min; MS (ESIneg): m/z=492 [M−H]⁻

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.275 (0.39), 0.288(1.76), 0.300 (1.96), 0.426 (1.56), 0.446 (1.69), 1.157 (0.32), 1.164(0.25), 1.175 (0.77), 1.183 (0.45), 1.194 (0.71), 1.213 (0.45), 1.233(0.36), 1.398 (2.08), 1.468 (16.00), 1.812 (5.38), 1.818 (5.49), 1.988(0.65), 2.273 (3.61), 2.328 (0.26), 2.469 (0.29), 2.670 (0.21), 2.746(9.82), 2.894 (0.19), 3.589 (0.16), 3.841 (1.73), 3.859 (1.71), 4.020(0.20), 4.038 (0.17), 4.857 (3.27), 7.157 (0.46), 7.163 (0.49), 7.178(0.88), 7.184 (0.95), 7.199 (0.50), 7.205 (0.53), 7.327 (0.46), 7.333(0.46), 7.354 (0.81), 7.377 (0.46), 7.382 (0.45), 7.555 (0.42), 7.576(0.87), 7.593 (0.84), 7.615 (0.38), 8.469 (0.90), 9.369 (0.51).

Example 369(±)-1-cyclopropyl-2-[5-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-1-yl]ethanol(racemate)

A microwave vial was charged with(±)-2-[5-amino-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-1-yl]-1-cyclopropylethanol(racemate, 185 mg, 672 μmol),4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (154 mg, 739 μmol)and sodium phenolate (85.8 mg, 739 μmol) and the contents were suspendedin 1,4-dioxane (2.3 mL). The reaction mixture was de gassed with Ar for3 min. Tris(dibenzylideneacetone)dipalladium (12.3 mg, 13.4 μmol) andXantPhos (15.6 mg, 26.9 μmol) were added and the reaction mixture wasdegassed again for 1 min. The vial was sealed and heated at 85° C.overnight while vigorously shaking. After cooling to ambienttemperature, the reaction mixture was diluted with dimethylsulfoxide,filtered and purified by preparative HPLC (method 6) to yield thedesired product (70 mg, 23% yield).

LC-MS (method 11): R_(t)=1.42 min; MS (ESIneg): m/z=446 [M−H]⁻

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.42), −0.008(3.82), 0.008 (3.44), 0.031 (0.64), 0.146 (0.40), 0.179 (0.75), 0.187(0.92), 0.200 (0.86), 0.253 (0.22), 0.274 (0.72), 0.289 (1.62), 0.308(1.66), 0.744 (0.47), 0.756 (0.80), 0.775 (0.76), 2.003 (16.00), 2.166(3.63), 2.328 (0.53), 2.332 (0.40), 2.367 (0.26), 2.523 (1.21), 2.628(13.81), 2.665 (0.46), 2.670 (0.56), 2.674 (0.42), 2.710 (0.29), 3.988(1.63), 4.890 (0.85), 6.140 (2.78), 7.245 (2.10), 7.267 (4.36), 7.289(2.40), 7.700 (1.68), 7.714 (2.11), 7.721 (2.05), 7.735 (1.64), 8.461(0.83), 9.270 (1.04).

Example 3701-cyclopropyl-2-[5-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-1-yl]ethanol

Obtained from separation of the enantiomers of a racemic sample of(±)-1-cyclopropyl-2-[5-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-1-yl]ethanol(racemate, 40.6 mg dissolved in 2-propanol/dichloromethane 1:1, 4 mL) bypreparative HPLC (Daicel Chiralpak IC 5 μm, 250×20 mm, flow: 15 mL/min,isocratic: 2-propanol/n-heptane 20/80) to yield the title compound asthe first eluting enantiomer (10.8 mg, 27% from racemate).

LC-MS (method 11): Rt=1.43 min; MS (ESIneg): m/z=446 [M−H]−

Chiral HPLC (Daicel IC-3 3 μm, 50×4.6 mm, isocratic i-hexane/2-propanol80/20): Rt=1.17 min, >99% ee

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.029 (0.94), 0.180(0.82), 0.189 (1.01), 0.201 (0.97), 0.289 (1.97), 0.309 (1.99), 0.756(0.89), 1.238 (0.17), 1.996 (16.00), 2.165 (4.58), 2.328 (0.44), 2.366(0.45), 2.624 (15.02), 2.670 (0.53), 2.710 (0.46), 3.336 (1.89), 3.352(0.74), 3.989 (2.11), 4.004 (1.89), 6.132 (3.31), 7.241 (2.22), 7.263(4.70), 7.286 (2.55), 7.696 (1.89), 7.710 (2.34), 7.717 (2.34), 7.731(1.82), 8.440 (0.97).

Example 3711-cyclopropyl-2-[5-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-1-yl]ethanol

Obtained from separation of the enantiomers of a racemic sample of(±)-1-cyclopropyl-2-[5-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-1-yl]ethanol(racemate, 40.6 mg dissolved in 2-propanol/dichloromethane 1:1, 4 mL) bypreparative HPLC (Daicel Chiralpak IC 5 μm, 250×20 mm, flow: 15 mL/min,isocratic: 2-propanol/n-heptane 20/80) to yield the title compound asthe second eluting enantiomer (11.2 mg, 28% from racemate).

LC-MS (method 11): Rt=1.43 min; MS (ESIneg): m/z=446 [M−H]⁻

Chiral HPLC (Daicel IC-3 3 μm, 50×4.6 mm, isocratic i-hexane/2-propanol80/20): Rt=2.27 min, 98.7% ee

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.178 (0.81), 0.188(0.97), 0.201 (0.93), 0.288 (1.70), 0.308 (1.73), 0.756 (0.81), 0.775(0.83), 1.105 (1.17), 1.120 (1.11), 1.136 (0.25), 1.154 (0.54), 1.172(0.30), 1.234 (0.25), 2.003 (16.00), 2.166 (3.99), 2.328 (0.33), 2.367(0.29), 2.628 (14.50), 2.669 (0.46), 2.710 (0.39), 2.911 (0.22), 2.929(0.22), 3.344 (1.05), 3.988 (1.71), 4.885 (1.23), 4.898 (1.22), 6.140(3.21), 7.245 (2.20), 7.267 (4.56), 7.289 (2.48), 7.700 (1.77), 7.714(2.26), 7.721 (2.20), 7.735 (1.82), 8.463 (1.10), 9.270 (1.48).

Example 372N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-[3,5-dimethyl-4-(5-methyl-1,3,4-oxadiazol-2-yl)-1H-pyrazol-1-yl]pyrimidin-4-amine

A solution ofN′-acetyl-1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbohydrazide(410 mg, 792 μmol) in tetrahydrofuran (40 ml, 490 mmol) was treated withBurges reagent (264 mg, 1.11 mmol) and stirred one hour at roomtemperature. Additional 1.4 equvialents of Burgess reagent (264 mg, 1.11mmol) were added and it was stirred again for one hour. The mixture wasdiluted with water and extracted with dichloromethane (3×). The combinedorganic phases were dried over magnesium sulfate and concentrated underreduced pressure. The crud eproduct was purified by preparative HPLC(method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent:A=water (0.01% formic acid), B=acetonitrile/gradient: 0.00-5.00 min=10%B, 6.50 min=20% B, 17.0-19.75 min=100% B, 19.75-23.00 min=90% B) toyield 259 mg (65%) of the desired product.

LC-MS (method 10): R_(t)=2.05 min; MS (ESIpos): m/z=500 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.304 (2.87), 0.314(2.91), 0.435 (3.11), 0.451 (3.15), 1.183 (0.50), 1.193 (0.89), 1.199(0.88), 1.208 (1.35), 1.218 (0.81), 1.223 (0.81), 1.232 (0.48), 2.021(15.22), 2.571 (16.00), 2.970 (15.84), 3.845 (2.10), 3.857 (2.03), 5.755(0.99), 7.260 (2.54), 7.277 (5.04), 7.295 (2.73), 7.736 (2.13).

Example 3734-[1-(cyclopropylmethyl)-5-({6-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidin-4-yl}amino)-4-methyl-1H-pyrazol-3-yl]benzonitrile

4-chloro-6-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidine(500 mg, 95% purity, 1.72 mmol) and sodium phenolate (219 mg, 1.89 mmol)were suspended in 1,4-dioxane (5.5 mL). The reaction mixture wasdegassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (47.2mg, 51.5 μmol), XantPhos (59.6 mg, 103 μmol) and4-[5-amino-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(530 mg, 90% purity, 1.89 mmol) were added and the reaction mixture wasdegassed again for 1 min. The reaction mixture was heated at 90° C. for3 h while vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with water and aqueous hydrochloric acid (1N) and extracted with ethyl acetate. The organic phase extract was driedover sodium sulfate and concentrated. The residue was purified by flashcolumn chromatography (SNAP Ultra 25 g, cyclohexane/ethyl acetategradient) to yield the desired product (427 mg, 49% yield).

LC-MS (method 9): R_(t)=1.28 min; MS (ESIpos): m/z=493 [M+H]⁺

¹H-NMR (600 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.310 (2.03), 0.318(2.12), 0.443 (2.27), 0.456 (2.34), 1.187 (0.23), 1.191 (0.33), 1.200(0.64), 1.204 (0.62), 1.212 (0.99), 1.220 (0.58), 1.225 (0.62), 1.233(0.34), 1.237 (0.24), 1.346 (0.26), 2.067 (16.00), 2.165 (0.35), 2.305(1.17), 2.337 (0.54), 2.386 (0.18), 2.760 (6.87), 3.873 (1.58), 3.883(1.56), 7.888 (1.47), 7.902 (7.16), 7.910 (4.24), 7.924 (1.10), 7.947(0.16), 7.961 (0.18), 8.026 (0.30), 8.040 (0.21), 8.540 (0.25), 9.595(0.20).

Example 374(±)-1-[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]-2,2,2-trifluoroethanol(racemate)

Molecular Sieves (4 Å) were placed in a round-bottom flask and dried ina vacuum drying-oven overnight at 120° C. After cooling to ambienttemperature, tetrabutylammonium fluoride trihydrate (179 mg, 640 μmol)and toluene (5.0 mL) were added and the suspension stirred for 30 min. Asolution of1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbaldehyde(95.0 mg, 213 μmol) in dichloromethane (1.0 mL) was then added, themixture was stired for 5 min and cooled to 0° C.Trimethyl(trifluoromethyl)silane (160 μL, 1.1 mmol) was then added andstirred at ambient temperature for 1.5 h. Furthermore,trimethyl(trifluoromethyl)silane (80 μL, 0.55 mmol), tetrabutylammoniumfluoride trihydrate (70 mg, 250 μmol) and dichloromethane (1 mL) wereadded and the reaction mixture stirred for another 1 h. The reactionmixture was diluted with ethyl acetate and water, the molecular sievesremoved by filtration and washed further with ethyl acetate. Afterseparation of the layers in the filtrate, the aqueous phase wasextracted again with ethyl acetate and the combined organic phaseextracts were dried over sodium sulfate and concentrated. The residuewas purified by flash column chromatography (SNAP Ultra 25 g,cyclohexane/ethyl acetate gradient 88/12 to 30/70) to yield the desiredproduct (43 mg, 39% yield).

LC-MS (method 11): R_(t)=1.43 min; MS (ESIpos): m/z=516 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (0.65), 0.006(0.41), 0.294 (2.49), 0.303 (2.51), 0.425 (2.66), 0.441 (2.68), 1.161(2.53), 1.176 (5.23), 1.181 (0.88), 1.190 (3.06), 1.197 (1.18), 1.206(0.69), 1.213 (0.69), 1.221 (0.36), 1.227 (0.27), 1.236 (0.19), 1.398(6.28), 1.967 (1.79), 1.989 (9.25), 2.008 (15.94), 2.238 (1.76), 2.363(0.20), 2.367 (0.16), 2.637 (0.20), 2.675 (16.00), 2.943 (0.66), 3.801(0.36), 3.830 (1.94), 3.843 (1.89), 4.009 (0.69), 4.023 (2.06), 4.038(2.03), 4.052 (0.67), 5.161 (0.67), 5.754 (11.43), 6.721 (1.03), 7.177(0.19), 7.193 (0.21), 7.244 (0.38), 7.255 (2.46), 7.262 (1.15), 7.273(4.88), 7.291 (2.62), 7.446 (0.24), 7.673 (0.26), 7.684 (0.31), 7.690(0.31), 7.702 (0.38), 7.718 (1.39), 7.729 (1.90), 7.744 (1.34), 8.486(0.44), 9.431 (0.35).

Example 3751-[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]-2,2,2-trifluoroethanol

Obtained from separation of the enantiomers of a racemic sample of(±)-1-[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]-2,2,2-trifluoroethanol(racemate, 118.0 mg dissolved in 2-propanol/dichloromethane/n-Heptane3:2:1, 6 mL) by preparative HPLC (Daicel Chiralpak IA 5 μm, 250×20 mm,flow: 15 mL/min, 40° C. isocratic: 2-propanol/n-heptane 10/90, 350 μL,per injection) to yield the title compound as the first elutingenantiomer (42.5 mg, 36% from racemate).

LC-MS (method 10): R_(t)=2.09 min; MS (ESIpos): m/z=516 [M+H]⁺

Chiral HPLC (Daicel IC-3 5 μm, 250×4.6 mm, flow: 1.0 mL/min isocratici-hexane/2-propanol 90/10): Rt=9.198 min, 97% ee

¹H-NMR (600 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.005 (0.56), 0.293(2.25), 0.301 (2.35), 0.426 (2.45), 0.440 (2.50), 1.184 (0.66), 1.188(0.66), 1.196 (1.07), 1.208 (0.61), 2.007 (15.49), 2.237 (1.64), 2.384(0.41), 2.673 (16.00), 3.830 (1.79), 3.841 (1.79), 5.155 (0.72), 6.679(1.64), 6.687 (1.64), 7.254 (2.15), 7.269 (4.40), 7.284 (2.35), 7.718(1.23), 7.728 (1.74), 7.740 (1.23).

Example 3761-[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]-2,2,2-trifluoroethanol

Obtained from separation of the enantiomers of a racemic sample of(±)-1-[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]-2,2,2-trifluoroethanol(racemate, 118.0 mg dissolved in 2-propanol/dichloromethane/n-Heptane3:2:1, 6 mL) by preparative (Daicel Chiralpak IA 5 μm, 250×20 mm, flow:15 mL/min, 40° C. isocratic: 2-propanol/n-heptane 10/90, 350 μL perinjection) to yield the title compound as the second eluting enantiomer(45.6 mg, 39% from racemate).

LC-MS (method 10): R_(t)=2.09 min; MS (ESIpos): m/z=516 [M+H]⁺

Chiral HPLC (Daicel IC-3 5 μm, 250×4.6 mm, flow: 1.0 mL/min, isocratici-hexane/2-propanol 90/10): Rt=11.10 min, 99% ee

¹H-NMR (600 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.005 (0.57), 0.284(1.13), 0.293 (2.51), 0.301 (2.55), 0.426 (2.79), 0.440 (2.75), 1.176(0.48), 1.184 (0.77), 1.188 (0.77), 1.196 (1.17), 1.209 (0.69), 1.966(4.08), 2.007 (15.52), 2.237 (1.66), 2.384 (0.40), 2.673 (16.00), 2.941(0.93), 3.801 (0.69), 3.813 (0.77), 3.830 (1.94), 3.841 (1.90), 5.157(0.73), 6.678 (1.74), 6.687 (1.78), 7.186 (0.40), 7.243 (0.61), 7.254(2.51), 7.258 (2.22), 7.269 (4.77), 7.284 (2.42), 7.443 (0.57), 7.673(0.57), 7.682 (0.65), 7.687 (0.65), 7.697 (0.57), 7.717 (1.33), 7.727(1.86), 7.740 (1.33).

Example 3772-{1-[6-({1,4-dimethyl-3-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3,5-dimethyl-1H-pyrazol-4-yl}propan-2-ol

Under an argon atmosphere, ethyl1-[6-({1,4-dimethyl-3-[4-(trifluoromethoxy)phenyl]-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3,5-dimethyl-1H-pyrazole-4-carboxylate(115 mg, 223 μmol) was dissolved in tetrahydrofuran (4.4 mL) and thesolution was cooled to 0° C. A solution of bromo(methyl)magnesium (1.1ml, 1.0 M, 1.1 mmol) was added dropwise and the reaction mixture wasstirred overnight at ambient temperature. The reaction mixture wascarefully quenched by addition of aqueous Na₂EDTA solution (10%) andethyl acetate was added. The organic phase extract was dried over sodiumsulfate and concentrated. The residue was purified by flash columnchromatography (SNAP Ultra 25 g, cyclohexane/ethyl acetate gradient 95/5to 5/95) to yield the desired product (20 mg, 18% yield).

LC-MS (method 10): R_(t)=2.06 min; MS (ESIpos): m/z=502 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.91), 0.008(0.77), 1.157 (0.42), 1.175 (0.80), 1.193 (0.41), 1.235 (0.29), 1.398(2.92), 1.468 (16.00), 1.909 (0.54), 1.988 (1.24), 2.037 (10.99), 2.272(2.94), 2.328 (0.24), 2.524 (0.48), 2.670 (0.21), 2.744 (11.24), 3.673(8.09), 4.021 (0.29), 4.039 (0.30), 4.859 (3.46), 7.417 (1.95), 7.438(2.18), 7.796 (2.73), 7.818 (2.45), 8.472 (0.74), 9.424 (1.56).

Example 3782-[1-(6-{[3-(2,4-difluorophenyl)-1,4-dimethyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]propan-2-ol

Under an argon atmosphere, ethyl1-(6-{[3-(2,4-difluorophenyl)-1,4-dimethyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(259 mg, 554 μmol) was dissolved in tetrahydrofuran (11 mL) and thesolution was cooled to 0° C. A solution of bromo(methyl)magnesium (2.8ml, 1.0 M, 2.8 mmol) was added dropwise and the reaction mixture wasstirred overnight at ambient temperature. The reaction mixture wascarefully quenched by addition of aqueous Na₂EDTA solution (10%) andethyl acetate was added. The organic phase was dried over sodium sulfateand concentrated. The residue was purified by flash columnchromatography (SNAP Ultra 25 g, cyclohexane/ethyl acetate gradient 95/5to 5/95) to yield the desired product (17 mg, 7% yield).

LC-MS (method 10): R_(t)=1.81 min; MS (ESIpos): m/z=454 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.64), 0.008(1.85), 1.157 (0.99), 1.175 (2.00), 1.193 (1.03), 1.471 (16.00), 1.816(4.76), 1.821 (5.54), 1.988 (3.56), 2.279 (4.09), 2.328 (0.41), 2.434(1.33), 2.471 (3.74), 2.670 (0.43), 2.747 (9.93), 2.895 (4.06), 3.671(7.28), 3.681 (3.06), 4.021 (0.85), 4.038 (0.84), 4.861 (3.32), 7.157(0.54), 7.176 (0.97), 7.197 (0.58), 7.330 (0.53), 7.355 (0.96), 7.374(0.52), 7.380 (0.54), 7.536 (0.46), 7.558 (1.04), 7.576 (0.94), 7.596(0.42), 8.479 (1.05), 9.420 (1.06).

Example 3792-{1-[6-({1,4-dimethyl-3-[4-(trifluoromethyl)phenyl]-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3,5-dimethyl-1H-pyrazol-4-yl}propan-2-ol

Under an argon atmosphere, ethyl1-[6-({1,4-dimethyl-3-[4-(trifluoromethyl)phenyl]-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3,5-dimethyl-1H-pyrazole-4-carboxylate(170 mg, 340 μmol) was dissolved in tetrahydrofuran and the solutioncooled to 0° C. A solution of bromo(methyl)magnesium (1.7 ml, 1.0 M, 1.7mmol) was added dropwise and the reaction mixture was stirred overnightat ambient temperature. The reaction mixture was carefully quenched byaddition of aqueous Na₂EDTA solution (10%) and ethyl acetate was added.The organic phase was separated, dried over sodium sulfate andconcentrated. The residue was purified by flash column chromatography(SNAP Ultra 25 g, cyclohexane/ethyl acetate gradient 95/5 to 5/95) toyield the desired product (90 mg, 54% yield).

LC-MS (method 10): R_(t)=2.03 min; MS (ESIpos): m/z=486 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.80), 0.008(0.88), 1.157 (0.98), 1.175 (1.98), 1.193 (1.01), 1.235 (0.17), 1.398(0.80), 1.470 (16.00), 1.989 (3.49), 2.071 (10.90), 2.274 (2.96), 2.328(0.27), 2.671 (0.24), 2.746 (11.21), 2.893 (0.17), 3.695 (8.24), 4.003(0.28), 4.021 (0.84), 4.039 (0.85), 4.056 (0.29), 4.861 (3.64), 7.781(2.05), 7.802 (2.82), 7.913 (2.48), 7.934 (1.83), 8.475 (0.88), 9.451(1.60).

Example 3802-[1-(6-{[1-(cyclopropylmethyl)-4-methyl-3-(pyridin-4-yl)-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]propan-2-ol

Under an argon atmosphere, ethyl1-(6-{[1-(cyclopropylmethyl)-4-methyl-3-(pyridin-4-yl)-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(120 mg, 254 μmol) was dissolved in tetrahydrofuran and the solutioncooled to 0° C. A solution of bromo(methyl)magnesium (2.5 ml, 1.0 M, 2.5mmol) was added dropwise and the reaction mixture was stirred overnightat ambient temperature. As low conversion was observed, a second aliquotof bromo(methyl)magnesium (2.5 ml, 1.0 M, 2.5 mmol) was added. After 3h, conversion was still low and a solution of chloro(methyl)magnesium(420 μl, 3.0 M, 1.3 mmol) was added. The reaction mixture was allowed tostir overnight. The reaction mixture was carefully quenched by additionof aqueous Na₂EDTA solution (10%) and ethyl acetate was added. Theorganic phase was separated, dried over sodium sulfate and concentrated.The residue was purified by flash column chromatography (SNAP Ultra 25g,cyclohexane/ethyl acetate gradient 95/5 to 5/95, followed bydichloromethane/methanol 4:1 isocratic) to yield the desired product (20mg, 16% yield).

LC-MS (method 11): R_(t)=0.92 min; MS (ESIpos): m/z=459 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (2.50), 0.008(2.12), 0.308 (2.34), 0.318 (2.61), 0.436 (2.21), 0.454 (2.36), 1.175(0.50), 1.210 (1.00), 1.234 (0.93), 1.465 (16.00), 1.908 (1.36), 1.988(0.47), 2.076 (12.83), 2.168 (1.23), 2.270 (2.65), 2.297 (1.40), 2.328(0.78), 2.367 (0.44), 2.632 (0.45), 2.670 (0.78), 2.691 (0.48), 2.711(0.56), 2.743 (12.49), 3.865 (2.16), 3.883 (2.24), 4.857 (3.34), 7.403(0.45), 7.425 (0.45), 7.687 (3.33), 7.702 (3.57), 8.462 (0.67), 8.606(3.98), 8.621 (4.24), 9.411 (0.79).

Example 381N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidin-4-amine

A microwave vial was charged with4-chloro-6-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidine(97.1 mg, 95% purity, 334 μmol) and1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine(100 mg, 90% purity, 367 μmol) and the contents were suspended in1,4-dioxane (1.1 mL). The reaction mixture was degassed with Ar for 3min. Tris(dibenzylideneacetone)dipalladium (6.11 mg, 6.67 μmol) andXantPhos (7.72 mg, 13.3 μmol) were added and the reaction mixture wasdegassed again for 1 min. Finally, sodium phenolate (42.6 mg, 367 μmol)was added to the reaction mixture. The vial was sealed and heated at 85°C. overnight while vigorously shaking. After cooling to ambienttemperature, the reaction mixture was filtered and concentrated. Theresidue was redissolved in dimethylsulfoxide and purified by preparativeHPLC (method 8) and further by flash column chromatography (SNAP Ultra10 g, cyclohexane/ethyl acetate 1:2) to yield the desired product (41mg, 24% yield).

LC-MS (method 10): R_(t)=2.54 min; MS (ESIpos): m/z=486 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.04), 0.008(0.89), 0.293 (2.35), 0.305 (2.59), 0.426 (2.45), 0.446 (2.62), 1.165(0.34), 1.177 (0.65), 1.184 (0.63), 1.196 (0.98), 1.208 (0.60), 1.215(0.61), 1.227 (0.31), 2.010 (16.00), 2.031 (0.29), 2.300 (1.84), 2.319(4.35), 2.322 (4.21), 2.367 (0.23), 2.524 (0.57), 2.671 (0.28), 2.675(0.21), 2.759 (7.87), 2.779 (3.45), 2.782 (3.37), 3.832 (2.04), 3.849(2.02), 7.252 (2.23), 7.274 (5.03), 7.289 (2.16), 7.292 (2.23), 7.296(2.72), 7.319 (1.70), 7.321 (1.76), 7.340 (0.86), 7.359 (0.55), 7.488(1.14), 7.509 (1.37), 7.523 (0.33), 7.528 (0.74), 7.712 (1.44), 7.726(1.89), 7.746 (1.31), 8.541 (0.34), 8.776 (1.22), 8.778 (1.20), 9.574(0.31).

Example 3826-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]-N-[3-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-5-yl]pyrimidin-4-amine

A microwave vial was charged with4-chloro-6-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidine(116 mg, 95% purity, 399 μmol) and3-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-5-amine (100 mg, 90% purity,439 μmol) and the contents were suspended in 1,4-dioxane (1.3 mL). Thereaction mixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (7.30 mg, 7.97 μmol) and XantPhos(9.23 mg, 15.9 μmol) were added and the reaction mixture was degassedagain for 1 min. Finally, sodium phenolate (50.9 mg, 439 μmol) was addedto the reaction mixture. The vial was sealed and heated at 85° C.overnight while vigorously shaking. After cooling to ambienttemperature, the reaction mixture was diluted with dimethylsulfoxide,filtered and purified by preparative HPLC (method 8) and further byflash column chromatography (SNAP Ultra 10 g, cyclohexane/ethyl acetategradient 88/12 to 0:100) to yield the desired product (41 mg, 24%yield).

LC-MS (method 10): R_(t)=2.34 min; MS (ESIpos): m/z=446 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.157 (0.64), 1.175(1.38), 1.193 (0.68), 1.399 (0.16), 1.989 (2.63), 2.018 (16.00), 2.074(0.20), 2.306 (2.43), 2.367 (0.30), 2.670 (0.54), 2.710 (0.28), 2.760(7.37), 3.666 (8.40), 4.021 (0.61), 4.038 (0.61), 4.057 (0.21), 7.245(1.92), 7.267 (3.94), 7.289 (2.17), 7.694 (1.54), 7.708 (1.91), 7.729(1.43), 8.552 (0.62), 9.622 (0.67).

Example 3836-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]-N-[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]pyrimidin-4-amine

A microwave vial was charged with4-chloro-6-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidine(116 mg, 95% purity, 399 μmol) and5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-amine (100 mg, 90% purity,439 μmol) and the contents were suspended in 1,4-dioxane (1.3 mL). Thereaction mixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (7.30 mg, 7.97 μmol) and XantPhos(9.23 mg, 15.9 μmol) were added and the reaction mixture was degassedagain for 1 min. Finally, sodium phenolate (50.9 mg, 439 μmol) wasadded, the vial was sealed and heated at 85° C. overnight whilevigorously shaking. After cooling to ambient temperature, the reactionmixture was filtered and concentrated. The residue was redissolved indimethylsulfoxide and purified by preparative HPLC (method X) to yieldthe desired product (20 mg, 11% yield).

LC-MS (method 9): R_(t)=1.27 min; MS (ESIpos): m/z=446 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.70), 0.008(1.84), 1.861 (10.88), 2.019 (0.77), 2.311 (7.12), 2.313 (7.35), 2.739(7.22), 2.742 (7.44), 3.666 (0.47), 3.686 (16.00), 7.358 (1.96), 7.363(0.81), 7.380 (4.55), 7.397 (0.91), 7.403 (2.74), 7.438 (0.75), 7.461(0.54), 7.511 (2.48), 7.516 (1.09), 7.524 (2.72), 7.532 (2.26), 7.541(0.90), 7.546 (1.94), 8.538 (2.92), 9.644 (1.38).

Example 384N-[1-(cyclopropylmethyl)-4-methyl-3-(pyridin-4-yl)-1H-pyrazol-5-yl]-6-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidin-4-amine

A microwave vial was charged with4-chloro-6-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidine(104 mg, 95% purity, 358 μmol) and1-(cyclopropylmethyl)-4-methyl-3-(pyridin-4-yl)-1H-pyrazol-5-amine (100mg, 90% purity, 394 μmol) and the contents were suspended in 1,4-dioxane(1.1 mL). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (6.56 mg, 7.17 μmol) and XantPhos(8.29 mg, 14.3 μmol) were added and the reaction mixture was degassedagain for 1 min. Finally, sodium phenolate (45.8 mg, 394 μmol) was addedand the vial was sealed and heated at 85° C. overnight while vigorouslyshaking. After cooling to ambient temperature, the reaction mixture wasfiltere, diluted with dimethylsulfoxide and purified by preparative HPLC(method 6) to yield the desired product (26 mg, 15% yield).

LC-MS (method 9): R_(t)=0.92 min; MS (ESIpos): m/z=469 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.17), −0.008(1.64), 0.008 (1.07), 0.309 (2.42), 0.321 (2.62), 0.438 (2.52), 0.458(2.67), 1.179 (0.35), 1.192 (0.67), 1.199 (0.65), 1.211 (1.01), 1.223(0.63), 1.229 (0.63), 1.241 (0.32), 2.083 (16.00), 2.241 (0.26), 2.304(1.94), 2.367 (0.27), 2.761 (8.09), 3.873 (2.14), 3.890 (2.10), 7.691(3.19), 7.706 (3.37), 8.546 (0.35), 8.610 (4.36), 8.625 (4.29), 9.617(0.35).

Example 385N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

Under an argon atmosphere4-chloro-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (150 mg,100% purity, 628 μmol) was dissolved in 1,4-dioxane (2.0 mL) and theresulting solution heated to 85° C.1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine(188 mg, 90% purity, 691 μmol), tris(dibenzylideneacetone)dipalladium(17.3 mg, 18.9 μmol) and XantPhos (21.8 mg, 37.7 μmol) were added andthe reaction mixture was degassed with Ar for 3 min. Finally, sodiumphenolate (80.3 mg, 691 μmol) was added and the reaction mixture wasdegassed again for 1 min. It was then heated at 85° C. for 4 h whilevigorously stirring. After cooling to ambient temperature, the reactionmixture was quenched by addition of aqueous hydrochloric acid (1 M). Itwas extracted with ethyl acetate (2×) and the combined organic phaseextracts were dried over sodium sulfate and concentrated. The residuewas purified by flash column chromatography (SNAP Ultra 25 g,cyclohexane/ethyl acetate gradient) to yield the desired product (202mg, 70% yield).

LC-MS (method 10): R_(t)=2.25 min; MS (ESIpos): m/z=448 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (0.43), 0.292(2.30), 0.301 (2.42), 0.423 (2.48), 0.439 (2.60), 1.162 (1.60), 1.168(0.43), 1.176 (3.36), 1.184 (0.74), 1.190 (2.02), 1.193 (1.14), 1.203(0.66), 1.208 (0.67), 1.397 (0.94), 1.989 (5.46), 2.006 (16.00), 2.179(2.21), 2.226 (0.46), 3.697 (9.47), 3.726 (0.61), 3.827 (2.02), 3.840(2.02), 4.010 (0.40), 4.024 (1.20), 4.038 (1.19), 7.256 (2.25), 7.274(4.52), 7.292 (2.41), 7.720 (1.37), 7.732 (1.86), 7.747 (1.32), 8.447(0.54), 9.357 (0.52).

Example 386(±)-1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3-methyl-4-(trifluoromethyl)-1,4,5,6-tetrahydrocyclopenta[c]pyrazol-4-ol(racemate)

Molecular Sieves (poweder, 4 Å) were placed in a round-bottom flask anddried in a vacuum drying-oven overnight at 120° C. After cooling toambient temperature, tetrabutylammonium fluoride trihydrate (214 mg, 765μmol) and toluene (5.0 mL) were added and the suspension stirred for 30min. A solution of1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3-methyl-5,6-dihydrocyclopenta[c]pyrazol-4(1H)-one(70.0 mg, 153 μmol) in dichloromethane (1.0 mL) was then added, themixture was stired for 5 min and cooled to 0° C.Trimethyl(trifluoromethyl)silane (180 μL, 1.2 mmol) was then added andthe reaction mixture was stirred at ambient temperature for 3.5 h. After2.5 h, dichloromethane (1 mL) was added to solubilize the reactioncomponents. The reaction mixture was diluted with ethyl acetate andwater, the molecular sieves removed by filtration and washed furtherwith ethyl acetate. After separation of the layers in the filtrate, theaqueous phase was extracted again with ethyl acetate and the combinedorganic phase extracts were dried over sodium sulfate and concentrated.The residue was purified by preparative HPLC (column: Chromatorex C18;125*30 mm, 10 μM, flow 75 mL/min, gradient acetonitrile/water(containing 0.1% trifluoroacetic acid) 5/95 to 95/5) to yield thedesired product (43 mg, 39% yield).

LC-MS (method 11): R_(t)=1.47 min; MS (ESIpos): m/z=528 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.150 (0.35), −0.022(0.51), −0.008 (3.03), 0.008 (2.18), 0.146 (0.32), 0.284 (2.61), 0.295(2.76), 0.416 (2.90), 0.436 (3.06), 0.918 (0.85), 0.936 (1.75), 0.955(0.82), 1.154 (0.46), 1.167 (0.81), 1.174 (0.78), 1.186 (1.19), 1.204(0.76), 1.234 (0.81), 1.283 (0.25), 1.302 (0.46), 1.320 (0.42), 1.337(0.21), 1.569 (0.28), 2.006 (16.00), 2.086 (0.38), 2.196 (2.37), 2.328(0.69), 2.366 (0.47), 2.523 (1.88), 2.670 (0.61), 2.710 (0.36), 2.877(0.56), 2.888 (0.71), 2.899 (0.86), 2.911 (1.22), 2.924 (0.69), 2.934(0.65), 2.944 (0.62), 3.069 (0.54), 3.082 (0.58), 3.091 (0.55), 3.103(0.55), 3.112 (1.02), 3.125 (1.07), 3.134 (0.94), 3.147 (0.81), 3.183(0.33), 3.217 (0.80), 3.228 (0.91), 3.239 (0.99), 3.249 (0.93), 3.260(0.69), 3.271 (0.73), 3.283 (0.83), 3.829 (2.11), 3.844 (2.08), 6.595(3.35), 7.255 (2.11), 7.277 (4.25), 7.299 (2.34), 7.736 (1.95), 8.460(0.44), 9.472 (0.36).

Example 387(±)-4-{5-[(6-{3,5-dimethyl-4-[2,2,2-trifluoro-1-hydroxyethyl]-1H-pyrazol-1-yl}pyrimidin-4-yl)amino]-1,4-dimethyl-1H-pyrazol-3-yl}benzonitrile(racemic)

Molecular sieves was suspended in toluene (8.0 ml, 75 mmol) andtetrabutylammonium fluoride hydrate (305 mg, 1.09 mmol) was added underan argon atmosphere. A solution of4-(5-{[6-(4-formyl-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-1,4-dimethyl-1H-pyrazol-3-yl)benzonitrile(150 mg, 364 μmol) in toluene (2 mL) and tetrahydrofuran (3 mL) wasadded and the resulting mixture was stirred 5 minutes at ambienttemperature. At 0° C. trimethyl(trifluoromethyl)silane (270 μl, 1.8mmol) was added and it was stirred for an addition hour at ambienttemperature. The mixture was diluted with water and extracted with ethylacetate (2×). The combined organic phases were dried over sodium sulfateand concentrated under reduced pressure. The crude product was purifiedby preparative HPLC (method 2) to yield 13.9 mg (8%) of the desiredproduct along with(±)-1-{1-[6-({3-[4-(2-amino-1,1,1,3,3,3-hexafluoropropan-2-yl)phenyl]-1,4-dimethyl-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3,5-dimethyl-1H-pyrazol-4-yl}-2,2,2-trifluoroethanolas by-product.

LC-MS (method 10): R_(t)=1.83 min; MS (ESIpos): m/z=483 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.07), 0.008(1.00), 2.073 (13.30), 2.247 (2.95), 2.676 (11.93), 3.697 (8.79), 5.152(0.57), 5.165 (0.68), 5.171 (0.64), 5.184 (0.57), 5.755 (2.32), 6.701(2.14), 6.714 (2.16), 7.896 (16.00), 8.497 (0.65), 9.521 (1.62).

Example 3886-(3,5-dimethyl-1H-pyrazol-1-yl)-N-{4-ethyl-3-(4-fluorophenyl)-1-[(2-methyl-2H-tetrazol-5-yl)methyl]-1H-pyrazol-5-yl}pyrimidin-4-amine

A microwave vial was charged with4-ethyl-3-(4-fluorophenyl)-1-[(2-methyl-2H-tetrazol-5-yl)methyl]-1H-pyrazol-5-amine(36.0 mg, 119 μmol), 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine(27.4 mg, 131 μmol) and sodium phenolate (15.3 mg, 131 μmol) and thecontents were suspended in 1,4-dioxane (0.41 mL). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium(2.19 mg, 2.39 μmol) and XantPhos (2.77 mg, 4.78 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously shaking. After coolingto ambient temperature, the reaction mixture was concentrated. Theresidue was redissolved in dimethylsulfoxide, filtered and purified bypreparative HPLC (method 3) to yield the desired product (14.8 mg, 24%yield).

LC-MS (method 11): R_(t)=1.42 min; MS (ESIpos): m/z=474 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.22), −0.008(1.66), 0.008 (1.73), 0.146 (0.19), 0.957 (4.36), 0.976 (9.81), 0.995(4.55), 1.566 (0.18), 1.647 (1.23), 2.179 (5.69), 2.187 (5.39), 2.327(0.41), 2.366 (0.42), 2.442 (0.95), 2.460 (2.59), 2.479 (2.83), 2.629(16.00), 2.654 (2.48), 2.670 (0.51), 2.710 (0.45), 4.217 (2.20), 5.468(3.31), 6.148 (3.52), 6.209 (0.55), 7.151 (0.16), 7.173 (0.22), 7.207(0.67), 7.254 (2.98), 7.276 (5.73), 7.299 (2.87), 7.330 (0.41), 7.348(0.32), 7.368 (0.92), 7.384 (0.96), 7.397 (1.11), 7.466 (0.29), 7.480(0.68), 7.500 (0.73), 7.520 (0.38), 7.656 (1.68), 7.671 (2.21), 7.690(1.56), 7.854 (0.19), 7.870 (0.20), 8.413 (0.94), 8.678 (0.53), 9.350(3.45).

Example 3892-[1-(6-{[1-(cyclopropylmethyl)-4-methyl-3-(4-methylphenyl)-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]propan-2-ol

Under an argon atmosphere a solution of ethyl1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(45.4 g, 95% purity, 88.1 mmol) in tetrahydrofuran (1.8 l) was treatedwith bromo(methyl)magnesium (150 ml, 3.0 M, 440 mmol) at 0° C. Theresulting mixture was allowed to warm up to ambient temperature and wasstirred overnight. The mixture was diluted with aqueous sodiumethylendiaminetetraacetic acid solution (450 mL, 10%) and stirred for 30minutes. 2000 mL water and ethyl acetate were added and the organicphase was separated and washed over sodium sulfate. The organic phasewas concentrated under reduced pressure and the crude product waspurified by flash-chromatography (cyclo-hexane/ethyl acetate 1:1) andMPLC-column (dichloromethane/acetone 8:2) to yield 930 mg (2.1%) of thedescribed product as a byproduct along with para-flour derivative.

LC-MS (method 9): R_(t)=1.04 min; MS (ESIpos): m/z=472 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.296 (2.31), 0.305(2.43), 0.425 (2.35), 0.441 (2.43), 1.187 (0.68), 1.193 (0.69), 1.196(0.57), 1.203 (1.06), 1.209 (0.58), 1.212 (0.64), 1.217 (0.63), 1.469(15.43), 1.766 (3.47), 2.006 (15.68), 2.076 (0.84), 2.226 (0.44), 2.245(0.80), 2.269 (1.86), 2.342 (13.08), 2.750 (16.00), 3.335 (14.61), 3.828(1.93), 3.842 (1.90), 4.859 (3.44), 7.243 (3.61), 7.258 (3.94), 7.272(0.42), 7.582 (3.12), 7.598 (2.75), 8.466 (0.57), 9.348 (0.50).

Example 390N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-{4-[(3,3-difluoroazetidin-1-yl)methyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-amine

A solution of1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbaldehyde(190 mg, 426 μmol) and 3,3-difluoroazetidine hydrochloride (1:1) (71.8mg, 554 μmol) in tetrahydrofuran (3.5 ml, 43 mmol) was treated withacetic acid (49 μl, 850 μmol) and stirred one hour at ambienttemperature. Subsequently sodium triacetoxyborohydride (145 mg, 682μmol) was added and the mixture was stirred overnight at ambienttemperature. The mixture was diluted with 3 mL water and purified bypreparative HPLC (method: column: Reprosil C18; 10 μm; 125×40 mm/flow:75 mL/min/solvent: A=water (0.1% formic acid), B=acetonitrile/grradient:0.00-5.50 min=10% B, 17.65-19.48 min=95% B, 19.66 min=10% B) andsubsequent by method 7 to yield 31.9 mg of the desired product (13%).

LC-MS (method 10): R_(t)=2.01 min; MS (ESIneg): m/z=521 [M−H]⁻

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.289 (2.97), 0.301(3.10), 0.419 (2.94), 0.439 (3.04), 1.181 (0.92), 1.193 (1.20), 2.003(16.00), 2.196 (3.35), 2.216 (3.04), 2.327 (1.04), 2.366 (0.76), 2.619(0.89), 2.650 (14.07), 2.709 (0.73), 3.487 (1.96), 3.518 (3.83), 3.545(4.55), 3.655 (0.63), 3.823 (2.81), 3.839 (2.75), 4.315 (0.47), 7.208(0.54), 7.251 (2.53), 7.273 (5.38), 7.295 (2.78), 7.498 (0.47), 7.712(1.80), 7.731 (2.47), 7.746 (1.80), 7.997 (0.54), 8.132 (2.06), 8.463(0.82), 8.675 (0.47), 9.379 (0.85).

Example 3916-(3,5-dimethyl-1H-pyrazol-1-yl)-N-{4-ethyl-3-(4-fluorophenyl)-1-[(1-methyl-1H-tetrazol-5-yl)methyl]-1H-pyrazol-5-yl}pyrimidin-4-amine

A microwave vial was charged with4-ethyl-3-(4-fluorophenyl)-1-[(1-methyl-1H-tetrazol-5-yl)methyl]-1H-pyrazol-5-amine(27.0 mg, 89.6 μmol),4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (20.6 mg, 98.6 μmol)and sodium phenolate (13.5 mg, 116 μmol) and the contents were suspendedin 1,4-dioxane (0.31 mL). The reaction mixture was degassed with Ar for3 min. Tris(dibenzylideneacetone)dipalladium (2.46 mg, 2.69 μmol) andXantPhos (3.11 mg, 5.38 μmol) were added and the reaction mixture wasdegassed again for 1 min. The vial was sealed and heated at 85° C.overnight while vigorously shaking. After cooling to ambienttemperature, the reaction mixture was filtered and concentrated. Theresidue was redissolved in dimethylsulfoxide and purified by preparativeHPLC (method 3) to yield the desired product (15.6 mg, 33% yield).

LC-MS (method 11): R_(t)=1.42 min; MS (ESIneg): m/z=472 [M−H]⁻

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.960 (4.09), 0.978(8.71), 0.997 (3.96), 1.646 (1.06), 2.191 (5.88), 2.327 (1.55), 2.366(0.98), 2.463 (8.96), 2.631 (15.04), 2.670 (1.53), 2.710 (0.84), 4.014(16.00), 5.616 (6.13), 6.157 (3.54), 7.256 (2.44), 7.279 (4.95), 7.301(2.71), 7.368 (0.96), 7.385 (1.01), 7.397 (1.08), 7.639 (2.04), 7.654(2.41), 7.675 (1.72), 8.398 (0.98), 9.435 (2.93).

Example 392(±)-1-[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]-2,2-difluoroethanol(racemate)

Molecular sieves (powder, 4 Å) and tetrabutylammonium fluoridetrihydrate (82.8 mg, 296 μmol) were flame-dried under vacuum. Aftercooling to ambient temperature, the mixture was suspended in toluene(1.5 mL) and stirred for 30 min. A solution of1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbaldehyde(44.0 mg, 98.8 μmol) in toluene (1 mL) was added and the reactionmixture stirred for 20 min. It was then cooled to −20° C. an(difluoromethyl)(trimethyl)silane (67 μl, 490 μmol) was added dropwise.The reaction mixture was allowed to warm to ambient temperature andstirred for 1 h. It was then quenched by addition of water and dilutedwith ethyl acetate. The molecular sieves was removed by filtration andfurther was with ethyl acetate. After separation of the layers in thefiltrate, the aqueous phase was further extracted with ethyl acetate andthe combined organic phase extracts dried over sodium sulfate andconcentrated. The residue was purified by preparative HPLC to yield thedesired product (11.3 mg, 23% yield).

LC-MS (method 11): R_(t)=1.37 min; MS (ESIpos): m/z=498 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.150 (0.16), −0.008(1.14), 0.008 (1.00), 0.290 (2.42), 0.302 (2.65), 0.421 (2.41), 0.441(2.56), 1.176 (0.65), 1.194 (1.06), 2.005 (16.00), 2.221 (2.66), 2.328(0.67), 2.366 (0.40), 2.524 (1.61), 2.646 (15.97), 2.670 (0.74), 2.710(0.43), 3.825 (2.27), 3.843 (2.25), 4.765 (0.70), 5.944 (0.41), 6.040(1.80), 6.073 (0.83), 6.083 (0.83), 6.223 (0.40), 7.250 (2.25), 7.272(4.69), 7.295 (2.54), 7.712 (1.54), 7.726 (2.01), 7.747 (1.44), 8.475(0.67), 9.401 (0.55).

Example 3931-[1-(6-{[1-(4-fluorophenyl)-3,5-dimethyl-1H-pyrazol-4-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]-2-methylpropan-2-ol

A solution of ethyl[1-(6-{[1-(4-fluorophenyl)-3,5-dimethyl-1H-pyrazol-4-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]acetate(80.0 mg, 173 μmol) in tetrahydrofuran (1.8 ml, 22 mmol) was treatedwith bromo(methyl)magnesium (200 μl, 3.0 M in diethyl ether, 600 μmol) t0° C. The mixture was stirred 30 min at ambient temperature andadditional 3.5 equivalents of bromo(methyl)magnesium solution (200 μl,3.0 M in diethyl ether, 600 μmol) were added. The mixture was stirredovernight at ambient temperature and diluted with water. The mixture wasextracted with ethyl acetate (3×). The combined organic phases weredried over sodium sulfate and concentrated under reduced pressure. Thecrude product was purified by preparative HPLC (method: column: ReprosilC18; 10 μm; 125×40 mm/flow: 75 mL/min/solvent: A=water (0.1% formicacid), B=acetonitrile/grradient: 0.00-5.50 min=10% B, 17.65-19.48min=95% B, 19.66 min=10% B) to yield 7 mg (9%) of the desired product).

LC-MS (method 10): R_(t)=1.72 min; MS (ESIpos): m/z=450 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.087 (14.16), 1.106(1.38), 1.358 (0.99), 2.081 (16.00), 2.181 (10.82), 2.565 (13.78), 3.363(0.78), 3.377 (1.24), 3.391 (1.17), 3.405 (0.61), 7.339 (1.80), 7.357(3.53), 7.374 (1.96), 7.594 (1.73), 8.387 (0.62), 8.816 (3.32).

Example 3941-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3-methyl-5,6-dihydrocyclopenta[c]pyrazol-4(1H)-one

Under an argon atmosphere,1-(6-chloropyrimidin-4-yl)-3-methyl-5,6-dihydrocyclopenta[c]pyrazol-4(1H)-one(500 mg, 2.01 mmol) and sodium phenolate (257 mg, 2.21 mmol) and thecontents were suspended in 1,4-dioxane (5.8 mL). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium(34.9 mg, 60.3 μmol), XantPhos (27.6 mg, 30.2 μmol) and1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine(543 mg, 2.21 mmol) were added and the reaction mixture was degassedagain for 1 min. The reaction mixture was heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was quenched with brine and extracted with ethylacetate (2×). The combined organic phase extracts were dried over sodiumsulfate and concentrated. The residue was purified by flash columnchromatography (SNAP Ultra 50 g, dichloromethane/methanol gradient 99/1to 90/10) and further purified by preparative HPLC (Kinetex C18 5 μm,150×30 mm, flow: 75 mL/min, 40° C., acetonitrile/water gradient 35/65 to95/5) to yield the desired product (195 mg, 19% yield).

LC-MS (method 9): R_(t)=1.08 min; MS (ESIpos): m/z=458 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.006 (0.88), 0.293(2.40), 0.300 (2.44), 0.425 (2.70), 0.441 (2.74), 1.168 (0.44), 1.178(0.81), 1.184 (0.78), 1.193 (1.13), 1.203 (0.74), 1.208 (0.74), 1.217(0.38), 2.015 (12.55), 2.305 (1.14), 2.360 (0.44), 2.364 (0.46), 2.520(0.50), 2.524 (0.34), 2.634 (0.17), 2.637 (0.23), 2.641 (0.16), 2.812(0.57), 2.937 (2.21), 2.946 (2.63), 3.322 (16.00), 3.338 (3.21), 3.343(2.86), 3.348 (3.06), 3.352 (2.67), 3.358 (2.62), 7.262 (1.82), 7.279(3.43), 7.297 (1.92), 7.739 (1.49), 8.503 (0.25), 9.587 (0.29).

Example 3952-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3-methyl-5,6-dihydrocyclopenta[c]pyrazol-4(2H)-one

Under an argon atmosphere,2-(6-chloropyrimidin-4-yl)-3-methyl-5,6-dihydrocyclopenta[c]pyrazol-4(2H)-one(1.70 g, 95% purity, 6.49 mmol) was dissolved in 1,4-dioxane (21 mL) andthe resulting solution was heated to 85° C. and degassed with argon for3 min.1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine(1.95 g, 90% purity, 7.14 mmol), tris(dibenzylidenaceton)dipalladium(178 mg, 195 μmol) and XantPhos (225 mg, 390 μmol) were added and themixture again degassed with argon for 1 min. Sodium phenolate (829 mg,7.14 mmol) was then added and the reaction mixture stirred at 85° C. for3.5 h. After cooling to ambient temperature, the reaction mixture wasquenched with aqueous hydrochloric acid solution (1 N) and extractedwith ethyl acetate (3×). The organic phase s were filtered, the filtratewas dried over sodium sulfate and concentrated. The residue was purifiedby flash column chromatography (SNAP Ultra 50g, cyclohexane/ethylacetate gradient) and further purified by preparative HPLC (column:Reprosil C18; 250*50 mm, 10 μM, flow 150 mL/min, gradientacetonitrile/water (containing 0.1% trifluoroacetic acid) 10/90 to90/10) to yield the desired product (714 mg, 23% yield).

LC-MS (method 11): Rt=1.36 min; MS (ESIpos): m/z=458 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (0.25), 0.296(1.48), 0.303 (1.49), 0.427 (1.71), 0.442 (1.71), 1.170 (0.28), 1.179(0.52), 1.185 (0.52), 1.194 (0.71), 1.204 (0.48), 1.209 (0.47), 1.219(0.24), 2.021 (11.58), 2.813 (16.00), 2.836 (1.17), 2.885 (1.23), 2.905(0.96), 2.919 (0.96), 2.952 (0.57), 3.332 (0.21), 3.844 (1.36), 3.855(1.32), 7.260 (1.65), 7.278 (3.39), 7.296 (1.97), 7.348 (0.19), 7.356(0.32), 7.357 (0.32), 7.499 (0.16), 7.514 (0.18), 7.743 (1.26), 8.568(0.21), 8.785 (0.23), 8.787 (0.23), 9.608 (0.18).

Example 3962-{1-[6-({1-(cyclopropylmethyl)-3-[4-(difluoromethyl)phenyl]-4-methyl-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3,5-dimethyl-1H-pyrazol-4-yl}propan-2-ol

A solution of ethyl1-[6-({1-(cyclopropylmethyl)-3-[4-(difluoromethyl)phenyl]-4-methyl-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3,5-dimethyl-1H-pyrazole-4-carboxylate(177 mg, 339 μmol) in tetrahydrofuran (3.5 ml, 44 mmol) was treated withchloro(methyl)magnesium (400 μl, 3.0 M in tetrahydrofuran, 1.2 mmol) at0° C. The mixture was stirred overnight at ambient temperature. As theconversion was not fully completed, the mixture was again cooled down to0° C. and additional 3.5 eq of chloro(methyl)magnesium solution (400 μl,3.0 M in tetrahydrofuran, 1.2 mmol) were added. The mixture was stirred3 hours at ambient temperature. The mixture was diluted with potassiumsodium tartrate solution and extracted with ethyl acetate (2×). Thecombined organic phases were dried over Extrelut NT3 and concentratedunder reduced pressure. The crude product was purified by preparativeHPLC (method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 50mL/min/solvent: A=water (0.01% formic acid), B=acetonitrile/grradient:0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75 min=100% B, 19.75-23.00min=90% B) to yield 112 mg (65%) of the desired product.

LC-MS (method 10): R_(t)=2.01 min; MS (ESIpos): m/z=508 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.307 (2.29), 0.317(2.40), 0.326 (0.68), 0.435 (2.38), 0.451 (2.55), 1.188 (0.44), 1.198(0.74), 1.204 (0.68), 1.214 (1.07), 1.220 (0.55), 1.223 (0.63), 1.228(0.66), 1.239 (0.69), 1.253 (0.86), 1.267 (0.52), 1.468 (15.78), 2.048(15.95), 2.087 (1.97), 2.149 (0.64), 2.272 (2.01), 2.748 (16.00), 3.856(1.94), 3.870 (1.88), 4.858 (3.61), 5.754 (1.75), 6.964 (1.46), 7.076(3.21), 7.188 (1.30), 7.638 (2.98), 7.654 (3.51), 7.845 (2.89), 7.861(2.45), 8.468 (0.57), 9.389 (0.56).

Example 3976-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-[1-(cyclopropylmethyl)-4-methyl-3-(6-methylpyridin-3-yl)-1H-pyrazol-5-yl]pyrimidin-4-amine

A solution of1-(cyclopropylmethyl)-4-methyl-3-(6-methylpyridin-3-yl)-1H-pyrazol-5-amine(100 mg, 413 μmol) in 1,4-dioxane (2.0 ml) was degassed with argon andheated to an internal temperature of 85° C. To the heated solution wasadded 4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (110mg, 454 μmol), tris(dibenzylidenaceton)dipalladium (11.3 mg, 12.4 μmol),Xantphos (13.1 mg, 24.8 μmol) and finally sodium phenolate (52.7 mg, 454μmol) before heating at 85° C. for an additional 30 minutes. Thereaction mixture was added to a saturated aqueous solution of sodiumhydrogen carbonate (11 mL), and the solution extracted three times withethyl acetate. The combined organic phase s were washed with a saturatedaqueous solution of sodium chloride, dried with sodium sulfate andconcentrated in vacuo. The crude product was purified byflash-chromatography on silica gel (Gradient 10% to 100% ethylacetate incyclohexane, column: Biotage SNAP Ultra 10 g) to yield 122 mg (100%purity, 66% yield) of the desired product.

LC-MS (Method 10): R_(t)=1.82 min; MS (ESIpos): m/z=449 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.293 (0.85), 0.305(0.95), 0.423 (0.86), 0.442 (0.93), 1.167 (0.12), 1.186 (0.23), 1.199(0.36), 1.217 (0.23), 1.236 (0.10), 2.014 (5.42), 2.210 (1.02), 2.539(16.00), 2.647 (6.50), 3.840 (0.84), 3.857 (0.81), 7.318 (0.85), 7.339(0.89), 7.944 (0.42), 7.959 (0.39), 8.497 (0.21), 8.757 (0.75), 9.480(0.16).

Example 3986-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-{1-(cyclopropylmethyl)-3-[4-(difluoromethoxy)phenyl]-4-methyl-1H-pyrazol-5-yl}pyrimidin-4-amine

A solution of1-(cyclopropylmethyl)-3-[4-(difluoromethoxy)phenyl]-4-methyl-1H-pyrazol-5-amine(100 mg, 341 μmol) in 1,4-dioxane (1.6 ml) was degassed with argon andheated to an internal temperature of 85° C. To the heated solution wasadded 4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (91.2mg, 375 μmol), tris(dibenzylidenaceton)dipalladium (9.37 mg, 10.2 μmol),Xantphos (10.8 mg, 20.5 μmol) and finally sodium phenolate (43.5 mg, 375μmol) before heating at 85° C. for an additional 30 minutes. To thereaction mixture at 85° C. was added additional portions of4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (45.6 mg,188 μmol), tris(dibenzylidenaceton)dipalladium (4.7 mg, 5.1 μmol),Xantphos (5.4 mg, 10.3 μmol) and sodium phenolate (22 mg, 188 μmol)before heating at 85° C. for a further 30 minutes. The reaction mixturewas added to a saturated solution of sodium hydrogen carbonate (9 mL),and the solution extracted three times with ethyl acetate. The combinedorganic phase s were washed with a saturated solution of sodiumchloride, dried with sodium sulfate and concentrated in vacuo. The crudeproduct was by flash-chromatography on silica gel (gradient 2% to 20%ethylacetate in cyclohexane, column: Biotage SNAP Ultra 10 g) to yield54.0 mg (100% purity, 32% yield) of the desired product.

LC-MS (Method 10): R_(t)=2.52 min; MS (ESIpos): m/z=500 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.301 (1.45), 0.420(1.35), 0.440 (1.43), 1.136 (0.18), 1.192 (0.55), 1.242 (0.20), 1.397(16.00), 2.011 (8.72), 2.207 (1.45), 2.647 (10.93), 3.828 (1.20), 7.093(1.20), 7.242 (2.42), 7.264 (2.58), 7.278 (2.56), 7.463 (1.17), 7.735(1.50), 7.756 (1.39), 8.486 (0.23), 9.462 (0.22).

Example 399N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-[3,5-dimethyl-4-(methylsulfanyl)-1H-pyrazol-1-yl]pyrimidin-4-amine

Under an argon atmosphere,6-(4-bromo-3,5-dimethyl-1H-pyrazol-1-yl)-N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]pyrimidin-4-amine(50.0 mg, 101 μmol) was dissolved in tetrahydrofuran (1.0 mL) and sodiumhydride (4.43 mg, 60% purity, 111 μmol) was added. The reaction mixturewas stirred for 10 min and was then cooled to −70° C. A solution ofn-butyllithium in hexanes (178 μL, 2.5 M, 440 μmol) was added. After 10min, (S)-methyl methanethiosulfonate (19 μl, 200 μmol) was added and thereaction mixture allowed to warm to ambient temperature. After reachingambient temperature, the reaction mixture was quenched with saturatedammonium chloride solution and diluted with water. It was extracted withethyl acetate (3×). The combined organic phase extracts were washed withbrine, dried over sodium sulfate and concentrated. The residue waspurified by preparative HPLC (column: Chromatorex C18; 125*30 mm, 10 μM,flow 100 mL/min, gradient acetonitrile/water (containing 0.1%trifluoroacetic acid) 10/90 to 90/10) to yield the desired product (22mg, 41% yield) along with a by-product(N-{1-(cyclopropylmethyl)-3-[4-fluoro-3-(methylsulfanyl)phenyl]-4-methyl-1H-pyrazol-5-yl}-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine,see below).

LC-MS (method 11): R_(t)=1.65 min; MS (ESIpos): m/z=464 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.019 (0.82), −0.007(0.27), 0.006 (0.20), 0.297 (2.37), 0.306 (2.50), 0.427 (2.64), 0.444(2.73), 0.852 (0.20), 1.170 (0.26), 1.176 (0.38), 1.185 (0.71), 1.191(0.78), 1.200 (1.11), 1.207 (0.74), 1.209 (0.74), 1.216 (0.77), 1.229(1.86), 1.340 (0.26), 1.988 (0.23), 2.013 (14.67), 2.029 (2.37), 2.135(5.48), 2.171 (7.92), 2.196 (0.86), 2.215 (0.33), 2.224 (0.42), 2.266(1.83), 2.309 (0.35), 2.421 (0.34), 2.432 (0.34), 2.582 (0.19), 2.632(1.87), 2.713 (0.17), 2.733 (16.00), 3.837 (1.91), 3.849 (2.00), 6.140(0.34), 7.257 (2.08), 7.261 (1.20), 7.275 (4.28), 7.293 (2.39), 7.298(0.82), 7.522 (0.19), 7.592 (0.22), 7.605 (0.22), 7.723 (1.25), 7.735(1.74), 7.750 (1.29), 8.499 (0.47), 9.454 (0.36).

Example 400N-[4-(difluoromethoxy)-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged with4-(difluoromethoxy)-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (300mg, 1.17 mmol) and 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine(268 mg, 1.28 mmol), and the contents were suspended in 1,4-dioxane (4.0mL). The reaction mixture was degassed with Ar for 5 min.Tris(dibenzylideneacetone)dipalladium (320 mg, 350 μmol), XantPhos (405mg, 700 μmol) and sodium phenolate (149 mg, 1.28 mmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously shaking. After coolingto ambient temperature, the reaction mixture was filtered andconcentrated. The residue was redissolved in dimethylsulfoxide andpurified by preparative HPLC (method 3) to yield the desired product(146 mg, 29% yield).

LC-MS (method 11): R_(t)=1.39 min; MS (ESIpos): m/z=430 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.196 (16.00), 2.629(12.16), 3.316 (13.56), 6.144 (3.48), 6.651 (1.49), 6.799 (2.88), 6.946(1.25), 7.342 (2.36), 7.386 (2.37), 7.391 (0.85), 7.400 (1.08), 7.404(4.95), 7.409 (0.95), 7.418 (0.89), 7.422 (2.68), 7.591 (2.65), 7.596(1.12), 7.602 (2.89), 7.609 (2.47), 7.616 (0.96), 7.620 (2.19), 8.461(3.81), 8.463 (3.66), 9.486 (3.10).

Example 401N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-[3,5-dimethyl-4-(methylsulfinyl)-1H-pyrazol-1-yl]pyrimidin-4-amine

N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-[3,5-dimethyl-4-(methylsulfanyl)-1H-pyrazol-1-yl]pyrimidin-4-amine(40.0 mg, 95% purity, 82.0 μmol) was dissolved in dichloromethane (2.0mL) and the solution cooled to 0° C. Meta-chloroperbenzoicacid (18.4 mg,77% purity, 82.0 μmol) was slowly added and the reaction mixture stirredfor 15 min at 0° C. It was then quenched by addition of aqueoussaturated sodium hydrogencarbonate solution, and extracted withdichloromethane (3×). The combined organic phase extracts were washedwith brine, dried over sodium sulfate and concentrated. The residue waspurified by preparative HPLC (column: Chromatorex C18; 120*30 mm, 10 μM,flow 75 mL/min, gradient acetonitrile/water (containing 0.1%trifluoroacetic acid) 10/90 to 90/10) to yield the desired product (16mg, 35% yield).

LC-MS (method 11): R_(t)=1.23 min; MS (ESIpos): m/z=480 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.08), 0.008(0.73), 0.290 (2.39), 0.302 (2.52), 0.424 (2.45), 0.443 (2.55), 0.917(0.20), 1.161 (1.00), 1.180 (1.90), 1.193 (1.10), 1.198 (1.21), 1.212(0.66), 1.231 (0.61), 1.246 (1.72), 1.262 (2.87), 1.279 (1.42), 1.408(2.79), 1.564 (0.16), 1.646 (0.27), 2.007 (14.00), 2.073 (0.28), 2.131(1.21), 2.162 (0.96), 2.328 (0.36), 2.367 (0.73), 2.410 (1.99), 2.560(0.54), 2.670 (0.25), 2.710 (0.28), 2.767 (16.00), 2.909 (8.18), 2.972(0.60), 3.011 (0.30), 3.080 (0.37), 3.092 (0.34), 3.098 (0.32), 3.110(0.35), 3.125 (0.22), 3.136 (0.20), 3.144 (0.18), 3.155 (0.19), 3.614(0.28), 3.624 (0.29), 3.640 (0.26), 3.831 (2.41), 3.848 (2.38), 6.970(0.37), 7.097 (0.42), 7.225 (0.44), 7.253 (1.92), 7.275 (3.99), 7.297(2.22), 7.713 (1.31), 7.728 (1.81), 7.747 (1.29), 8.524 (0.38), 9.536(0.34).

Example 4021-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-N,N,3,5-tetramethyl-1H-pyrazole-4-carboxamide

A solution of1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylicacid (360 mg, 780 μmol) and N-methylmethanamine (430 2.0 M intetrahydrofuran, 860 μmol) in dimethylformamide (6.7 ml, 88 mmol) wastreated with N,N-diisopropylethylamine (410 μl, 2.3 mmol) and HATU (386mg, 1.01 mmol). The mixture was stirred overnight at ambienttemperature. The mixture was diluted with saturated sodium hydrogencarbonate solution and extracted with ethyl acetate (3×). The combinedorganic phases were washed with brine, dried over sodium sulfate andconcentrated under reduced pressure. The crude product was purified bypreparative HPLC (method: column: Reprosil C18; 10 μm; 125×40 mm/flow:75 mL/min/solvent: A=water (0.1% formic acid), B=acetonitrile/grradient:0.00-5.50 min=10% B, 17.65-19.48 min=95% B, 19.66 min=10% B) to yield340 mg (89%) of the desired product.

LC-MS (method 10): R_(t)=1.84 min; MS (ESIpos): m/z=489 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.295 (2.18), 0.306(2.35), 0.426 (2.28), 0.446 (2.39), 1.074 (0.41), 1.091 (0.82), 1.109(0.41), 1.179 (0.62), 1.187 (0.60), 1.198 (0.94), 1.210 (0.57), 1.217(0.57), 2.012 (13.19), 2.150 (2.19), 2.586 (16.00), 2.906 (3.01), 2.978(3.29), 3.375 (0.42), 3.392 (0.41), 3.832 (1.91), 3.848 (1.91), 7.253(1.97), 7.275 (4.18), 7.298 (2.32), 7.717 (1.23), 7.731 (1.72), 7.751(1.30), 8.500 (0.50), 9.452 (0.41).

Example 403(±)-2-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3-methyl-4-(trifluoromethyl)-2,4,5,6-tetrahydrocyclopenta[c]pyrazol-4-ol(racemate)

Molecular Sieves (4 Å) and tetrabutylammonium fluoride trihydrate (110mg, 393 μmol) were placed in a round-bottom flask and flame-dried. Aftercooling to ambient temperature, tetrabutylammonium under an argonatmosphere, it was suspended in toluene (2 mL) and the suspension wasstirred at ambient temperature for 30 min.2-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3-methyl-5,6-dihydrocyclopenta[c]pyrazol-4(2H)-one(75.0 mg, 80% purity, 131 μmol) was added and the reaction mixturestirred for 5 min before being cooled to 0° C.trimethyl(trifluoromethyl)silane (97 μl, 660 μmol) was added dropwiseand the reaction mixture was allowed to stir overnight at ambienttemperature. Further batches of dry molecular sieves (4 Å),tetrabutylammonium fluoride (110 mg, 393 μmol) andtrimethyl(trifluoromethyl)silane (97 μl, 660 μmol) were added and thereaction mixture was stirred for another 3 h. Further batches of drymolecular sieves (4 Å), tetrabutylammonium fluoride (110 mg, 393 μmol)and trimethyl(trifluoromethyl)silane (97 μl, 660 μmol) were added andthe reaction mixture was stirred for another 1 h. Further batches of drymolecular sieves (4 Å), tetrabutylammonium fluoride (110 mg, 393 μmol)and trimethyl(trifluoromethyl)silane (97 μl, 660 μmol) were added andthe reaction mixture was stirred for another 1 h. The reaction mixturewas then quenched by addition of water and diluted with ethyl acetate.The solids were removed by filtration and the layers in the filtrateseparated. The aqueous phase was extracted with ethyl acetate. Thecombined organic phase extracts were washed with brine, dried oversodium sulfate and concentrated. The residue was purified by preparativeHPLC (column: Chromatorex C18; 125*30 mm, 10 μM, flow 75 mL/min,gradient acetonitrile/water (containing 0.1% trifluoroacetic acid) 10/90to 90/10) to yield the desired product (34 mg, 47% yield).

LC-MS (method 11): R_(t)=1.43 min; MS (ESIpos): m/z=528 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.021 (0.18), −0.006(1.01), 0.006 (0.56), 0.288 (1.96), 0.296 (2.01), 0.419 (2.20), 0.435(2.24), 1.161 (0.37), 1.171 (0.67), 1.176 (0.67), 1.186 (0.94), 1.200(0.62), 1.210 (0.33), 1.233 (0.18), 2.013 (16.00), 2.074 (0.19), 2.422(0.71), 2.435 (0.55), 2.672 (15.24), 2.697 (0.68), 2.800 (0.89), 2.943(0.42), 2.965 (0.26), 3.834 (2.03), 3.847 (1.98), 4.329 (0.22), 6.651(0.17), 7.257 (2.34), 7.275 (4.78), 7.293 (2.57), 7.335 (0.16), 7.728(1.39), 7.740 (1.89), 7.754 (1.34), 8.514 (0.45), 9.471 (0.44).

Example 404(±)-2-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,4-dimethyl-2,4,5,6-tetrahydrocyclopenta[c]pyrazol-4-ol(racemate)

Under an argon atmosphere,2-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3-methyl-5,6-dihydrocyclopenta[c]pyrazol-4(2H)-one(80.0 mg, 80% purity, 140 μmol) was dissolved in tetrahydrofuran and thesolution cooled to 0° C. A solution of bromo(methyl)magnesium (700 μl,1.0 M in tetrahydrofuran, 700 μmol) was added dropwise and the reactionmixture was allowed to slowly warm to ambient temperature and stirredfor 2 h. The reaction mixture was carefully quenched by addition ofaqueous Na₂EDTA solution (10%) and extracted with ethyl acetate (3×).The combined organic phase extracts were washed with brine, dried oversodium sulfate and concentrated. The residue was purified by flashcolumn chromatography (SNAP Ultra 10 g, cyclohexane/ethyl acetategradient) and further purified by preparative HPLC (column: ChromatorexC18; 125*30 mm, 10 μM, flow 75 mL/min, gradient acetonitrile/water 10/90to 90/10) to yield the desired product (30 mg, 45% yield).

LC-MS (method 10): R_(t)=1.92 min; MS (ESIpos): m/z=474 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.284 (1.88), 0.294(2.04), 0.413 (1.97), 0.433 (2.10), 1.181 (0.81), 1.470 (7.75), 2.007(14.48), 2.289 (0.91), 2.304 (1.80), 2.323 (1.25), 2.655 (16.00), 2.710(0.57), 3.827 (2.15), 3.844 (2.08), 5.030 (3.48), 7.252 (2.07), 7.274(4.27), 7.296 (2.27), 7.721 (1.44), 7.735 (1.82), 7.742 (1.77), 7.756(1.36), 8.469 (0.78), 9.363 (0.87).

Example 405(±)-cyclopropyl[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]methanol(racemate)

Under an argon atmosphere,1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbaldehyde(80.0 mg, 180 μmol) was dissolved in tetrahydrofuran and the solutioncooled to 0° C. A solution of bromo(cyclopropyl)magnesium (1.8 ml, 0.50M in tetrahydrofuran, 900 μmol) was added dropwise and the reactionmixture was stirred for 1 h at ambient temperature. The reaction mixturewas carefully quenched by addition of aqueous Na₂EDTA solution (10%) andextracted with ethyl acetate (2×). The combined organic phase extractswere dried over sodium sulfate and concentrated. The residue waspurified by flash column chromatography (SNAP Ultra 25 g,cyclohexane/ethyl acetate gradient 95/5 to 20/80) to yield the desiredproduct (49 mg, 56% yield).

LC-MS (method 11): R_(t)=1.38 min; MS (ESIpos): m/z=488 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.008 (0.53), 0.120(0.83), 0.132 (1.01), 0.141 (0.71), 0.292 (2.44), 0.304 (2.85), 0.316(1.17), 0.328 (0.88), 0.348 (1.76), 0.365 (1.83), 0.380 (1.02), 0.391(0.72), 0.422 (2.44), 0.442 (2.60), 0.481 (0.65), 0.499 (0.86), 0.514(0.85), 0.526 (0.39), 1.157 (1.03), 1.175 (2.30), 1.183 (1.37), 1.193(1.92), 1.214 (1.04), 1.233 (0.46), 1.398 (0.88), 1.988 (2.69), 2.007(14.02), 2.199 (0.29), 2.250 (2.92), 2.328 (0.35), 2.366 (0.20), 2.626(16.00), 2.670 (0.45), 2.710 (0.27), 3.827 (2.28), 3.844 (2.30), 3.949(0.90), 3.957 (0.99), 3.968 (0.99), 3.976 (0.97), 4.002 (0.28), 4.021(0.66), 4.038 (0.65), 4.056 (0.24), 4.958 (2.09), 4.966 (2.15), 5.754(2.47), 7.251 (1.94), 7.274 (4.14), 7.296 (2.31), 7.713 (1.42), 7.728(1.92), 7.734 (1.93), 7.748 (1.51), 8.457 (0.62), 9.352 (0.73).

Example 4066-(4-bromo-3,5-dimethyl-1H-pyrazol-1-yl)-N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]pyrimidin-4-amine

Under an argon atmosphere,4-(4-bromo-3,5-dimethyl-1H-pyrazol-1-yl)-6-chloropyrimidine (1.00 g, 95%purity, 3.30 mmol) was suspended in 1,4-dioxane (11 mL). The reactionmixture was degassed with Ar for 3 min and heated to 85° C.1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine(991 mg, 90% purity, 3.63 mmol), tris(dibenzylideneacetone)dipalladium(90.8 mg, 99.1 μmol) and XantPhos (115 mg, 198 μmol) were added and wasdegassed again for 1 min. Finally, sodium phenolate (422 mg, 3.63 mmol)were added and the reaction mixture was heated at 85° C. for 3 h whilevigorously stirring. After cooling to ambient temperature, the reactionmixture was quenched with aqueous hydrochloric acid solution (1 N) andextracted with ethyl acetate. The organic phase extracts were filteredand dried over sodium sulfate. The residue was purified by flash columnchromatography (SNAP Ultra 50 g, cyclohexane/ethyl acetate gradient toyield the desired product (1.04 g, 60% yield).

LC-MS (method 10): R_(t)=2.56 min; MS (ESIpos): m/z=496 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.289 (1.68), 0.301(1.81), 0.421 (1.72), 0.441 (1.82), 1.174 (0.49), 1.193 (0.71), 1.398(16.00), 2.005 (10.52), 2.205 (1.84), 2.328 (0.16), 2.367 (0.24), 2.660(12.10), 2.710 (0.18), 3.826 (1.59), 3.843 (1.57), 7.252 (1.51), 7.274(3.02), 7.296 (1.63), 7.713 (1.02), 7.727 (1.39), 7.747 (0.93), 8.502(0.39), 9.469 (0.28).

Example 407N-{3-[4-(difluoromethyl)phenyl]-1,4-dimethyl-1H-pyrazol-5-yl}-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (99.9 mg, 479 μmol)and 3-[4-(difluoromethyl)phenyl]-1,4-dimethyl-1H-pyrazol-5-amine (125mg, 527 μmol) and the contents were suspended in 1,4-dioxane (1.8 ml, 21mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (13.2 mg, 14.4 μmol) and Xantphos(16.6 mg, 28.7 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (61.2 mg, 527 μmol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was filtered and purified bypreparative HPLC (method: column: Reprosil C18; 10 gm; 125×30 mm/flow:50 mL/min/solvent: A=water (0.01% formic acid),B=acetonitrile/grradient: 0.00-5.00 min=10% B, 6.50 min=20% B,17.0-19.75 min=100% B, 19.75-23.00min=90% B) to yield the desiredproduct (100 mg, 48%).

LC-MS (method 10): R_(t)=2.05 min; MS (ESIpos): m/z=410 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.904 (16.00), 1.981(0.91), 2.199 (15.29), 2.243 (0.55), 2.632 (13.78), 2.718 (0.46), 3.569(1.69), 3.707 (1.00), 5.166 (0.65), 6.164 (3.99), 7.031 (1.31), 7.143(2.77), 7.254 (1.20), 7.457 (3.04), 7.633 (3.57), 7.649 (4.25), 7.742(4.05), 7.758 (3.09), 8.519 (4.59), 9.805 (0.54).

Example 4086-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]-N-{3-[4-(difluoromethyl)phenyl]-1,4-dimethyl-1H-pyrazol-5-yl}pyrimidin-4-amine

A microwave vial was charged4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (117mg, 479 μmol) and3-[4-(difluoromethyl)phenyl]-1,4-dimethyl-1H-pyrazol-5-amine (125 mg,527 μmol) and the contents were suspended in 1,4-dioxane (1.8 ml, 21mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (13.2 mg, 14.4 μmol) and Xantphos(16.6 mg, 28.7 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (61.2 mg, 527 μmol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with water andextracted with dichloromethane (2×). The combined organic phases weredried over sodium sulfate and concentrated under reduced pressure. Thecrude product was purified by preparative HPLC (method 4) to yield thedesired product (39.0 mg, 17%).

LC-MS (method 10): R_(t)=2.17 min; MS (ESIpos): m/z=446 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.886 (9.21), 2.299(13.47), 3.736 (16.00), 6.774 (3.77), 7.024 (1.16), 7.136 (2.47), 7.248(1.01), 7.442 (0.55), 7.633 (2.66), 7.650 (3.41), 7.723 (1.11), 7.738(3.20), 7.754 (2.32), 7.832 (2.23), 7.941 (0.90), 8.485 (2.70), 9.621(1.32).

Example 409N-{5-[4-(difluoromethyl)phenyl]-1,4-dimethyl-1H-pyrazol-3-yl}-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (72.0 mg, 345 μmol),5-[4-(difluoromethyl)phenyl]-1,4-dimethyl-1H-pyrazol-3-amine (90.0 mg,379 μmol) and sodium phenolate (44.0 mg, 379 μmol) and the contents weresuspended in 1,4-dioxane (1.3 ml, 15 mmol). The reaction mixture wasdegassed with Ar for 3 min. Tris(dibenzylidenaceton)dipalladium (9.47mg, 10.3 μmol) and Xantphos (12.0 mg, 20.7 μmol) were added and thereaction mixture was degassed again for 1 min. The vial was sealed andheated at 85° C. overnight while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with water andextracted with dichloromethane (2×). The combined organic phases weredried over sodium sulfate and concentrated under reduced pressure. Thecrude product was purified by preparative HPLC (method 3) to yield thedesired product (50.7 mg, 36%).

LC-MS (method 10): R_(t)=2.06 min; MS (ESIpos): m/z=410 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.063 (16.00), 2.177(2.14), 2.634 (11.00), 3.323 (14.41), 6.145 (2.13), 6.962 (1.13), 7.074(2.38), 7.186 (1.00), 7.633 (2.24), 7.649 (2.57), 7.837 (2.17), 7.853(1.83), 8.479 (0.60), 9.439 (1.53).

Example 4104-[3-({6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-yl}amino)-4-methoxy-1-methyl-1H-pyrazol-5-yl]benzonitrile

A microwave vial was charged4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (487mg, 1.99 mmol) and4-(3-amino-4-methoxy-1-methyl-1H-pyrazol-5-yl)benzonitrile (500 mg, 2.19mmol) and the contents were suspended in 1,4-dioxane (12 ml, 140 mmol).The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (54.7 mg, 59.7 μmol) and Xantphos(69.1 mg, 119 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (254 mg, 2.19 mmol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was filtered and purified bypreparative HPLC (method: column: Reprosil C18; 10 μm; 125×30 mm/flow:50 mL/min/solvent: A=water (0.01% formic acid),B=acetonitrile/grradient: 0.00-5.00 min=10% B, 6.50 min=20% B,17.0-19.75 min=100% B, 19.75-23.00 min=90% B) to yield the desiredproduct (373 mg, 43%).

LC-MS (method 9): R_(t)=1.04 min; MS (ESIpos): m/z=437 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.288 (9.06), 3.564(16.00), 3.784 (0.53), 3.794 (11.99), 6.774 (2.71), 7.246 (3.11), 7.248(3.02), 7.716 (0.75), 7.780 (3.19), 7.784 (1.13), 7.794 (1.32), 7.798(3.52), 7.824 (1.62), 7.933 (0.65), 8.005 (0.86), 8.008 (3.80), 8.012(1.19), 8.022 (1.27), 8.026 (3.12), 8.487 (2.09), 9.644 (0.63).

Example 4114-[5-({6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-yl}amino)-4-methoxy-1-methyl-1H-pyrazol-3-yl]benzonitrile

A microwave vial was charged4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (97.4mg, 398 μmol) and4-(5-amino-4-methoxy-1-methyl-1H-pyrazol-3-yl)benzonitrile (100 mg, 438μmol) and the contents were suspended in 1,4-dioxane (3.2 ml, 37 mmol).The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (10.9 mg, 11.9 μmol) and Xantphos(13.8 mg, 23.9 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (50.9 mg, 438 _(t)tmol) was added. The vial was sealed andheated at 85° C. for 120 minutes while vigorously stirring. Aftercooling to ambient temperature, the reaction mixture was diluted withhydrochlorid acid and extracted with ethyl acetate (2×). The combinedorganic phases were washer with water and brine, dried over sodiumsulfate and concentrated under reduced pressure. The crude product waspurified by flash-chromatography (column: SNAP Ultra 10 g, solvent.dichloromethane/ethyl acetate 4:1) to yield the desired product (136 mg,78%).

LC-MS (method 10): R_(t)=2.04 min; MS (ESIpos): m/z=437 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.615 (0.48), 2.289(2.65), 3.633 (0.43), 3.659 (6.23), 3.728 (16.00), 6.798 (2.27), 7.685(0.94), 7.821 (2.01), 7.873 (2.72), 7.894 (3.53), 7.957 (0.84), 8.034(3.12), 8.055 (2.39), 8.534 (0.85), 9.703 (0.83).

Example 412N-[4-(difluoromethoxy)-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-amine

A microwave vial was charged with4-(difluoromethoxy)-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (120mg, 467 μmol) and4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (126mg, 513 μmol), and the contents were suspended in 1,4-dioxane (1.6 mL).The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (128 mg, 140 μmol) and XantPhos(162 mg, 280 μmol) were added and the reaction mixture was degassedagain for 1 min. Finally, sodium phenolate (59.6 mg, 513 μmol) was addedand the vial was sealed and heated at 85° C. overnight while vigorouslyshaking. After cooling to ambient temperature, the reaction mixture wasfiltered and concentrated. The residue was redissolved indimethylsulfoxide and purified by preparative HPLC (method 6) andrepurified by flash column chromatography (SNAP Ultra 10 g,cyclohexane/ethyl acetate gradient 100/0 to 50/50) to yield the desiredproduct (71 mg, 32% yield).

LC-MS (method 11): R_(t)=1.45 min; MS (ESIpos): m/z=466 [M+H]⁺

¹H-NMR (600 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.308 (14.67), 3.741(16.00), 5.748 (2.58), 6.673 (1.30), 6.780 (3.84), 6.796 (2.53), 6.919(1.12), 7.380 (1.29), 7.390 (2.29), 7.393 (0.86), 7.401 (0.98), 7.404(4.42), 7.408 (0.96), 7.416 (0.79), 7.419 (2.46), 7.597 (2.28), 7.601(1.02), 7.606 (2.52), 7.612 (2.31), 7.617 (0.89), 7.620 (2.08), 7.738(0.98), 7.829 (2.18), 7.920 (0.86), 8.494 (3.20), 9.684 (1.97).

Example 4136-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-[4-(difluoromethoxy)-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]pyrimidin-4-amine

A microwave vial was charged with4-(difluoromethoxy)-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (100mg, 389 μmol),4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (104 mg,428 μmol) and the contents were suspended in 1,4-dioxane (1.4 mL). Theresulting reaction mixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (107 mg, 117 μmol) and XantPhos(135 mg, 233 μmol) were added and the reaction mixture was degassedagain for 1 min. Finally, sodium phenolate (49.6 mg, 428 μmol) was addedand the vial was sealed and heated at 85° C. overnight while vigorouslyshaking. After cooling to ambient temperature, the reaction mixture wasfiltered and concentrated. The residue was redissolved indimethylsulfoxide and purified by preparative HPLC (method 6) to yieldthe desired product (59 mg, 33% yield).

LC-MS (method 11): R_(t)=1.55 min; MS (ESIpos): m/z=464 [M+H]⁺

¹H NMR (500 MHz, dimethylsulfoxide-d₆) δ ppm: 2.23 (s, 3H), 2.65 (s,3H), 3.73 (s, 3H), 6.80 (t, J=74 Hz, 1H), 7.33-7.46 (m, 3H), 7.55-7.66(m, 2H), 8.50 (s, 1H), 9.61 (s, 1H).

Example 4146-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-[3-(4-fluorophenyl)-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-yl]pyrimidin-4-amine

A solution of1-(cyclopropylmethyl)-4-methyl-3-(6-methylpyridin-3-yl)-1H-pyrazol-5-amine(100 mg, 413 μmol) in 1,4-dioxane (1.5 ml) was degassed with argon andheated to an internal temperature of 85° C. To the heated solution wasadded 3-(4-fluorophenyl)-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-amine(88.0 mg, 353 μmol), tris(dibenzylidenaceton)dipalladium (8.82 mg, 9.63μmol), Xantphos (10.2 mg, 19.3 μmol) and finally sodium phenolate (41.0mg, 353 μmol) before heating at 85° C. for an additional 30 minutes. Thereaction mixture was added to a saturated aqueous solution of sodiumhydrogen carbonate (180 mL), and the solution extracted three times withethyl acetate. The combined organic phase s were washed with a saturatedsolution of sodium chloride, dried with sodium sulfate and concentratedin vacuo. The crude product was purified by flash-chromatography onsilica gel (Gradient 18% to 100% ethylacetate in cyclohexane, column:Biotage SNAP Ultra 10 g) to yield 91.0 mg (100% purity, 62% yield) ofthe desired product.

LC-MS (Method 9): R_(t)=1.27 min; MS (ESIpos): m/z=456 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.002 (13.79), 2.205(1.68), 2.646 (16.00), 3.142 (2.96), 3.647 (1.55), 3.658 (3.06), 3.669(1.57), 4.112 (0.94), 7.257 (1.72), 7.261 (0.72), 7.275 (3.49), 7.293(1.88), 7.716 (0.96), 7.727 (1.31), 7.743 (0.96), 8.503 (0.45), 9.419(0.92).

Example 415N-[1-(cyclopropylmethyl)-4-methyl-3-(6-methylpyridin-3-yl)-1H-pyrazol-5-yl]-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-amine

In a sealed microwave tube under argon,1-(cyclopropylmethyl)-4-methyl-3-(6-methylpyridin-3-yl)-1H-pyrazol-5-amine(60.0 mg, 248 μmol),4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (66.6mg, 272 μmol), (31.6 mg, 272 μmol), (6.80 mg, 7.43 μmol), (7.85 mg, 14.9μmol) were dissolved in 1,4-dioxane (1.2 ml). The reaction mixture washeated at 90° C. for 30 minutes. The cooled reaction mixture was dilutedwith ethylacetate, washed with a saturated aqueous solution of sodiumhydrogen carbonate and the aqueous phase then extracted twice withethylacetate. The combined organic phase s were dried with sodiumsulfate and concentrated in vacuo. The crude product was purified byflash-chromatography on silica gel (Gradient 18% to 100% ethylacetate incyclohexane, column: Biotage SNAP Ultra 10 g) to yield the desiredproduct 57.4 mg (100% purity, 51% yield).

LC-MS (Method 10): R_(t)=1.60 min; MS (ESIpos): m/z=451 [M+H]⁺

¹H-NMR (500 MHz, CHLOROFORM-d) δ [ppm]: 0.335 (0.68), 0.345 (2.84),0.356 (2.88), 0.366 (0.73), 0.556 (0.75), 0.566 (2.36), 0.568 (2.36),0.582 (2.44), 0.594 (0.58), 1.269 (0.61), 1.275 (0.59), 1.285 (0.93),1.295 (0.55), 1.301 (0.59), 1.316 (0.28), 2.122 (16.00), 2.248 (0.16),2.302 (12.32), 2.615 (15.34), 3.952 (3.20), 3.966 (3.14), 6.594 (3.59),6.728 (0.55), 6.848 (0.56), 7.236 (2.14), 7.252 (2.24), 7.644 (1.18),7.753 (2.36), 7.863 (1.09), 7.969 (1.67), 7.974 (1.64), 7.986 (1.59),7.990 (1.54), 8.529 (3.96), 8.530 (4.07), 8.871 (2.34), 8.875 (2.21).

Example 4162-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-1,2,4,5,6,7-hexahydro-3H-indazol-3-one

A solution ofN-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-hydrazinylpyrimidin-4-amine(95.0 mg, 70% purity, 188 μmol) in methanol (2.0 ml, 49 mmol) wastreated with methyl 2-oxocyclohexanecarboxylate (28 μl, 190 μmol) andstirred for 4 hours at 80° C. The mixture was concentrated under reducedpressure and purified by preparative HPLC ((method: column: ReprosilC18; 10 μm; 125×40 mm/flow: 75 mL/min/solvent: A=water (0.1% formicacid), B=acetonitrile/gradient: 0.00-5.50 min=10% B, 17.65-19.48 min=95%B, 19.66 min=10% B) and subsequent by using (method 18) to yield 12.0 mg(14%) of the desired product.

LC-MS (method 10): R_(t)=2.01 min; MS (ESIpos): m/z=460 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.277 (2.99), 0.286(3.13), 0.407 (2.84), 0.423 (2.97), 1.071 (0.66), 1.085 (1.32), 1.099(0.67), 1.156 (0.49), 1.166 (0.85), 1.170 (0.86), 1.180 (1.19), 1.190(0.80), 1.195 (0.78), 1.204 (0.42), 1.353 (0.44), 1.624 (1.88), 1.632(1.96), 1.682 (1.97), 1.692 (1.88), 1.993 (16.00), 2.118 (1.83), 2.446(1.81), 2.458 (2.98), 3.355 (0.59), 3.369 (0.79), 3.383 (0.72), 3.827(2.49), 3.840 (2.40), 7.251 (2.51), 7.268 (4.90), 7.286 (2.60), 7.697(2.51), 7.709 (3.04), 7.715 (2.89), 7.726 (2.31), 8.424 (0.98), 9.393(3.80), 11.409 (2.35).

Example 4176-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-{1-(cyclopropylmethyl)-4-methyl-3-[4-(methylamino)phenyl]-1H-pyrazol-5-yl}pyrimidin-4-amine

In a sealed microwave tube under argon,1-(cyclopropylmethyl)-4-methyl-3-[4-(methylamino)phenyl]-1H-pyrazol-5-amine(60.0 mg, 234 μmol),4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (62.6 mg,257 μmol), (29.9 mg, 257 μmol), (6.43 mg, 7.02 μmol), (7.42 mg, 14.0μmol) were dissolved in 1,4-dioxane (1.1 ml). The reaction mixture washeated at 90° C. for 45 minutes. The cooled reaction mixture was dilutedwith dichloromethane, washed with a saturated aqueous solution of sodiumhydrogen carbonate and the aqueous phase then extracted twice withdichloromethane. The combined organic phase s were dried with sodiumsulfate and concentrated in vacuo. The crude product was purified byflash-chromatography on silica gel (Gradient 8% to 60% ethylacetate incyclohexane, column: Biotage SNAP Ultra 10 g) to yield the desiredproduct 75.3 mg (100% purity, 69% yield).

LC-MS (Method 10): R_(t)=2.33 min; MS (ESIpos): m/z=463 [M+H]⁺

¹H-NMR (600 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.279 (1.55), 0.408(1.78), 0.421 (1.82), 1.173 (0.82), 1.184 (0.53), 1.960 (11.87), 2.198(1.12), 2.644 (16.00), 2.703 (9.03), 2.712 (9.13), 3.784 (1.35), 3.794(1.35), 5.708 (0.69), 5.746 (0.20), 6.589 (3.72), 6.604 (3.82), 7.429(1.45), 7.442 (1.41), 8.486 (0.22), 9.389 (0.18).

Example 418 ethyl1-(6-{[1-(cyclopropylmethyl)-4-methyl-3-(6-methylpyridin-3-yl)-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

In a sealed microwave tube under argon,1-(cyclopropylmethyl)-4-methyl-3-(6-methylpyridin-3-yl)-1H-pyrazol-5-amine(150 mg, 619 μmol), ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (191mg, 681 μmol), tris(dibenzylidenaceton)dipalladium (17.0 mg, 18.6 μmol),Xantphos (19.6 mg, 37.1 μmol) were dissolved in 1,4-dioxane (3.0 ml).The reaction mixture was heated to 90° C. and after 2 minutes was addedsodium phenolate (79.0 mg, 681 μmol), and the reaction continuedstirring for an additional 30 minutes. The cooled reaction mixture wasdiluted with dichloromethane, washed with a saturated aqueous solutionof sodium hydrogen carbonate and the aqueous phase then extracted twicewith dichloromethane. The combined organic phase s were dried withsodium sulfate and concentrated in vacuo. The crude product was purifiedby flash-chromatography on silica gel (Gradient 20% to 100% ethylacetatein cyclohexane, column: Biotage SNAP Ultra 10 g) to yield 181 mg (100%purity, 60% yield) of the desired product.

LC-MS (Method 10): R_(t)=1.69 min; MS (ESIpos): m/z=487 [M+H]⁺

¹H-NMR (500 MHz, CHLOROFORM-d) δ [ppm]: 0.008 (12.21), 0.014 (0.36),0.338 (0.54), 0.348 (2.19), 0.359 (2.17), 0.369 (0.61), 0.558 (0.63),0.568 (1.80), 0.570 (1.78), 0.574 (0.85), 0.584 (1.88), 0.586 (1.71),0.596 (0.50), 1.250 (0.14), 1.264 (0.30), 1.274 (0.45), 1.280 (0.45),1.290 (0.74), 1.300 (0.43), 1.304 (0.41), 1.316 (0.27), 1.364 (4.47),1.378 (9.65), 1.393 (4.54), 2.119 (13.19), 2.423 (10.66), 2.610 (12.82),2.988 (16.00), 3.952 (2.56), 3.966 (2.52), 4.304 (1.33), 4.318 (4.23),4.332 (4.16), 4.347 (1.28), 6.678 (0.44), 6.876 (0.37), 7.229 (1.72),7.245 (1.79), 7.958 (1.48), 7.962 (1.48), 7.974 (1.39), 7.978 (1.39),8.587 (3.75), 8.589 (3.70), 8.858 (1.82), 8.861 (1.80).

Example 419cyclopropyl[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]methanol

Obtained from separation of the enantiomers of a racemic sample of(±)-1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbaldehyde(racemate 49 mg dissolved in ethanol/n-heptane 1:2, 3 mL) by preparativeHPLC (Daicel Chiralpak IG 5 μm, 250×20 mm, 35° C., flow: 15 mL/min,isocratic ethanol/n-heptane 90/10, injections of 0.4 mL every 17 min) toyield the title compound as the first eluting enantiomer (18 mg, 37%from racemate).

LC-MS (method 11): R_(t)=1.37 min; MS (ESIpos): m/z=488 [M+H]⁺

Chiral HPLC (Daicel Chiralpak IG 5 μm, 250×4.6 mm, isocratici-hexane/ethanol 90/10 +0.2% diethylamine) Rt=11.7 min, 99% ee

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (1.38), 0.007(0.83), 0.293 (0.95), 0.303 (0.99), 0.349 (0.48), 0.363 (0.55), 0.369(0.46), 0.424 (1.00), 0.440 (1.02), 1.186 (0.54), 1.196 (0.68), 1.210(0.42), 1.378 (16.00), 1.387 (14.69), 1.818 (0.52), 1.828 (0.67), 1.839(0.74), 2.007 (6.37), 2.250 (0.85), 2.626 (8.04), 2.941 (0.49), 3.424(0.72), 3.446 (0.58), 3.452 (0.59), 3.468 (0.46), 3.484 (1.26), 3.491(0.78), 3.504 (0.51), 3.543 (0.46), 3.551 (0.50), 3.634 (0.63), 3.655(0.48), 3.696 (0.61), 3.718 (0.53), 3.828 (0.79), 3.841 (0.77), 4.958(0.76), 4.964 (0.77), 7.255 (0.96), 7.273 (1.94), 7.291 (1.04), 7.717(0.55), 7.728 (0.73), 7.745 (0.54).

Example 420cyclopropyl[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]methanol

Obtained from separation of the enantiomers of a racemic sample of(±)-1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbaldehyde(racemate 49 mg dissolved in ethanol/n-heptane 1:2, 3 mL) by preparativeHPLC (Daicel Chiralpak IG 5 μm, 250×20 mm, 35° C., flow: 15 mL/min,isocratic ethanol/n-heptane 90/10, injections of 0.4 mL every 17 min) toyield the title compound as the second eluting enantiomer (18 mg, 37%from racemate).

LC-MS (method 11): R_(t)=1.37 min; MS (ESIpos): m/z=488 [M+H]⁺

Chiral HPLC (Daicel Chiralpak IG 5 μm, 250×4.6 mm, isocratici-hexane/ethanol 90/10 +0.2% diethylamine) Rt=13.2 min, 99%ee

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.120 (0.17), −0.007(1.99), 0.007 (1.11), 0.116 (0.66), 0.122 (0.71), 0.132 (0.81), 0.293(2.12), 0.303 (2.19), 0.331 (0.71), 0.349 (1.04), 0.363 (1.24), 0.379(0.81), 0.388 (0.58), 0.424 (2.19), 0.440 (2.25), 0.495 (0.78), 0.501(0.75), 0.511 (0.63), 1.141 (0.27), 1.156 (0.66), 1.170 (0.88), 1.186(1.19), 1.196 (1.46), 1.210 (0.93), 1.388 (0.17), 2.007 (13.07), 2.251(1.89), 2.362 (0.30), 2.626 (16.00), 3.828 (1.77), 3.841 (1.71), 3.958(0.81), 3.967 (0.80), 4.958 (1.76), 4.964 (1.69), 7.255 (1.99), 7.273(3.93), 7.291 (2.05), 7.717 (1.23), 7.729 (1.66), 7.744 (1.16), 8.455(0.50), 9.347 (0.46).

Example 421N-[1-(cyclopropylmethyl)-3-(5-fluoropyridin-2-yl)-4-methyl-1H-pyrazol-5-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (86.6 mg, 415 μmol)and1-(cyclopropylmethyl)-3-(5-fluoropyridin-2-yl)-4-methyl-1H-pyrazol-5-amine(225 mg, 50% purity, 457 μmol) and the contents were suspended in1,4-dioxane (1.6 ml, 19 mmol). The reaction mixture was degassed with Arfor 3 min. Tris(dibenzylidenaceton)dipalladium (11.4 mg, 12.5 μmol) andXantphos (14.4 mg, 24.9 μmol) were added and the reaction mixture wasdegassed again for 1 min and heated to 85° C. At this temperature andsodium phenolate (53.0 mg, 457 μmol) was added. The vial was sealed andheated at 85° C. for 90 minutes while vigorously stirring. After coolingto ambient temperature, the reaction mixture was left overnight andpurified by preparative HPLC (method: column: Reprosil C18; 10 μm;125×30 mm/flow: 50 mL/min/solvent: A=water (0.01% formic acid),B=acetonitrile/grradient: 0.00-5.00 min=10% B, 6.50 min=20% B,17.0-19.75 min=100% B, 19.75-23.00 min=90% B) and subsequently byflash-chromatography (column: SNAP KP-Sil 10 g, solvent: 96%dichloromethane/4% ethyl acetate to 66% dichloromethane/34% ethylacetate to 54% dichloromethane/46% ethyl acetate) to yield the desiredproduct (45.3 mg, 25%).

LC-MS (method 10): R_(t)=2.19 min; MS (ESIpos): m/z=419 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.311 (1.79), 0.320(1.84), 0.404 (0.41), 0.416 (0.41), 0.437 (1.99), 0.453 (2.00), 1.198(0.58), 1.204 (0.57), 1.213 (0.88), 1.220 (0.48), 1.223 (0.55), 1.229(0.58), 1.519 (1.31), 2.154 (16.00), 2.171 (1.55), 2.629 (12.81), 3.864(1.43), 3.877 (1.38), 6.136 (1.70), 7.755 (0.55), 7.761 (0.61), 7.773(1.16), 7.779 (1.24), 7.790 (0.67), 7.796 (0.68), 7.996 (0.69), 8.005(0.76), 8.013 (0.69), 8.022 (0.61), 8.462 (0.42), 8.595 (2.28), 8.601(2.26), 9.395 (0.44), 9.664 (0.49).

Example 422N-[1-(cyclopropylmethyl)-3-(5-fluoropyridin-2-yl)-4-methyl-1H-pyrazol-5-yl]-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-amine

A microwave vial was charged4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (102mg, 415 μmol) and1-(cyclopropylmethyl)-3-(5-fluoropyridin-2-yl)-4-methyl-1H-pyrazol-5-amine(225 mg, 50% purity, 457 μmol) and the contents were suspended in1,4-dioxane (1.6 ml, 19 mmol). The reaction mixture was degassed with Arfor 3 min. Tris(dibenzylidenaceton)dipalladium (11.4 mg, 12.5 μmol) andXantphos (14.4 mg, 24.9 μmol) were added and the reaction mixture wasdegassed again for 1 min and heated to 85° C. At this temperature andsodium phenolate (53.0 mg, 457 μmol) was added. The vial was sealed andheated at 85° C. for 90 minutes while vigorously stirring. After coolingto ambient temperature, the reaction mixture was left overnight andpurified by preparative HPLC (method: column: Reprosil C18; 10 μm;125×30 mm/flow: 50 mL/min/solvent: A=water (0.01% formic acid),B=acetonitrile/grradient: 0.00-5.00 min=10% B, 6.50 min=20% B,17.0-19.75 min=100% B, 19.75-23.00min=90% B) and subsequently byflash-chromatography (column: SNAP KP-Sil 10 g, solvent: 96%dichloromethane/4% ethyl acetate to 34% ethyl acetate) to yield thedesired product (36.4 mg, 18%).

LC-MS (method 10): R_(t)=2.23 min; MS (ESIpos): m/z=455 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.847 (0.68), 2.193(0.55), 2.197 (0.75), 2.201 (0.53), 3.026 (16.00).

Example 423N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-[3,5-dimethyl-4-(methylsulfonyl)-1H-pyrazol-1-yl]pyrimidin-4-amine

N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-[3,5-dimethyl-4-(methylsulfanyl)-1H-pyrazol-1-yl]pyrimidin-4-amine(20.0 mg, 95% purity, 41.0 μmol) was dissolved in dichloromethane (1.0mL) and cooled to 0° C. Meta-chloroperbenzoic acid (18.4 mg, 77% purity,82.0 μmol) was added slowly and the reaction mixture stirred for 30 minat 0° C. The reaction was quenched by careful addition of aqueoussaturated sodium hydrogencarbonate solution and extracted withdichloromethane (3×). The combined organic phase extracts were washedwith brine, dried over sodium sulfate and concentrated. The residue waspurified by preparative HPLC (column: Chromatorex C18; 125*30 mm, 10 μM,flow 75 mL/min, gradient acetonitrile/water (containing 0.1%trifluoroacetic acid) 10/90 to 90/10) to yield the desired product (6mg, 28% yield).

LC-MS (method 11): R_(t)=1.34 min; MS (ESIneg): m/z=494 [M−H]⁻

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (1.65), 0.007(0.90), 0.293 (2.45), 0.302 (2.51), 0.428 (2.73), 0.444 (2.76), 1.169(0.45), 1.179 (0.78), 1.185 (0.74), 1.194 (1.13), 1.204 (0.71), 1.209(0.74), 1.234 (0.30), 2.009 (16.00), 2.045 (0.38), 2.168 (0.22), 2.233(0.26), 2.390 (1.39), 2.620 (0.18), 2.631 (0.54), 2.876 (10.29), 3.384(0.26), 3.836 (1.84), 3.847 (1.81), 4.354 (0.20), 7.256 (2.30), 7.274(4.56), 7.292 (2.47), 7.727 (2.01), 8.549 (0.31), 9.576 (0.21).

Example 424N-[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]-6-[4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidin-4-amine

A microwave vial was charged4-chloro-6-[4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidine (100 mg, 402μmol) and 5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-amine (90.8 mg,442 μmol) and the contents were suspended in 1,4-dioxane (1.7 ml, 20mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (4.79 mg, 5.23 μmol) and Xantphos(6.98 mg, 12.1 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (70.0 mg, 603 μmol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was left overnight, dilutedwith water and extracted with dichloromethane (2×). The combined organicphases were dried over sodium sulfate and concentrated under reducedpressure. The crude product was purified by preparative HPLC (method:column: Reprosil C18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent: A=water(0.01% formic acid), B=acetonitrile/grradient: 0.00-5.00 min=10% B, 6.50min=20% B, 17.0-19.75 min=100% B, 19.75-23.00 min=90% B) to yield thedesired product (90.2 mg, 54%).

LC-MS (method 11): R_(t)=1.46 min; MS (ESIneg): m/z=416 [M−H]⁻

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (0.44), 2.026(16.00), 3.677 (5.60), 7.254 (1.75), 7.272 (3.47), 7.290 (1.87), 7.707(1.19), 7.719 (1.62), 7.734 (1.11), 9.187 (3.39), 9.760 (0.51).

Example 425(±)-4-{5-[(6-{3,5-dimethyl-4-[2,2,2-trifluoro-1-hydroxyethyl]-1H-pyrazol-1-yl}pyrimidin-4-yl)amino]-4-methoxy-1-methyl-1H-pyrazol-3-yl}benzonitrile(racemic)

Under an argon atmosphere a Schlenk tube was charged with molecularsieves in toluene (6 mL). To this mixture tetrabutylammonium fluoridehydrate (256 mg, 917 μmol) was added and the mixture was stirred atambient temperature for 30 minutes. Subsequently a solution of4-(5-{[6-(4-formyl-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-4-methoxy-1-methyl-1H-pyrazol-3-yl)Dbenzonitrile(131 mg, 306 μmol) in toluene (3 mL) was added and it was stirred for 5minutes. Then, trimethyl(trifluoromethyl)silane (230 μl, 1.5 mmol) at−18° C. was added and the reaction mixture was stirred 10 minutes at−18° C. and one hour at ambient temperature. The mixture was dilutedwith water, filtered and extracted with ethyl acetate (2×). The combinedorganic phases were dried over sodium sulfate, concentrated underreduced pressure and the crude product was purified using preparativeHPLC (method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 50mL/min/solvent: A=water (0.01% formic acid), B=acetonitrile/grradient:0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75 min=100% B, 19.75-23.00min=90% B) and by (method 7) to yield the desired product (30.2 mg,20%).

LC-MS (method 10): R_(t)=1.82 min; MS (ESIpos): m/z=499 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.078 (1.50), 1.092(3.10), 1.106 (1.51), 2.250 (1.77), 2.684 (8.33), 3.363 (0.50), 3.377(1.48), 3.391 (1.45), 3.405 (0.47), 3.656 (5.09), 3.729 (16.00), 5.170(0.41), 6.709 (1.45), 6.719 (1.46), 7.872 (2.58), 7.875 (0.99), 7.885(1.13), 7.889 (3.12), 8.035 (2.78), 8.038 (0.99), 8.048 (0.97), 8.052(2.13), 8.525 (0.73), 9.574 (0.71).

Example 426N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-[4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidin-4-amine

A microwave vial was charged4-chloro-6-[4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidine (100 mg, 402μmol) and1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine(109 mg, 442 μmol) and the contents were suspended in 1,4-dioxane (1.7ml, 20 mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (4.79 mg, 5.23 μmol) and Xantphos(6.98 mg, 12.1 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (70.0 mg, 603 μmol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. The mixture was leftovernight at ambient temperature, diluted with water and dichloromethane(2×). The combined organic phases were dried over sodium sulfate andconcentrated under reduced pressure. The crude product was purified bypreparative HPLC (method: column: Reprosil C18; 10 μm; 125×30 mm/flow:50 mL/min/solvent: A=water (0.01% formic acid),B=acetonitrile/grradient: 0.00-5.00 min=10% B, 6.50 min=20% B,17.0-19.75 min=100% B, 19.75-23.00 min=90% B) and byflash-chromatography (column: SNAP KP-Sil 10 g, solvent: 96%dichloromethane/4% ethyl acetate to 34% ethyl acetate) to yield thedesired product (87.8 mg, 48%).

LC-MS (mehtod 10): R_(t)=2.32 min; MS (ESIpos): m/z=458 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.296 (1.34), 0.418(1.35), 0.433 (1.35), 1.190 (0.56), 2.017 (16.00), 3.850 (1.09), 7.262(1.40), 7.280 (2.79), 7.298 (1.50), 7.739 (1.22), 9.181 (3.15).

Example 427N-[3-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-5-yl]-6-[4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidin-4-amine

A microwave vial was charged4-chloro-6-[4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidine (100 mg, 402μmol) and 3-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-5-amine (90.8 mg,442 μmol) and the contents were suspended in 1,4-dioxane (1.7 ml, 20mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (4.79 mg, 5.23 μmol) and Xantphos(6.98 mg, 12.1 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (70.0 mg, 603 μmol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. The mixture was leftovernight at ambient temperature, diluted with water and dichloromethane(2×). The combined organic phases were dried over sodium sulfate andconcentrated under reduced pressure. The crude product was purified bypreparative HPLC (method: column: Reprosil C18; 10 μm; 125×30 mm/flow:50 mL/min/solvent: A=water (0.01% formic acid), B=acetonitrile/gradient:0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75 min=100% B, 19.75-23.00min=90% B) and by flash-chromatography (column: SNAP KP-Sil 10 g,solvent: 96% dichloromethane/4% ethyl acetate to 45% ethyl acetate) toyield the desired product (66.9 mg, 40%).

LC-MS (method 10): R_(t)=2.19 min; MS (ESIpos): m/z=418 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.880 (9.59), 3.328(16.00), 7.368 (2.31), 7.372 (0.91), 7.382 (1.26), 7.386 (4.93), 7.390(1.12), 7.399 (1.00), 7.404 (2.77), 7.522 (0.49), 7.528 (2.77), 7.532(1.31), 7.539 (3.10), 7.545 (2.57), 7.552 (1.15), 7.556 (2.24), 8.337(4.37), 8.560 (2.52), 9.166 (3.34), 9.789 (1.45).

Example 4284-[5-({6-[4-(2-hydroxy-2-methylpropyl)-3,5-dimethyl-1H-pyrazol-1-yl]pyrimidin-4-yl}amino)-4-methoxy-1-methyl-1H-pyrazol-3-yl]benzonitrile

Under an argon atmosphere a solution of ethyl[1-(6-{[3-(4-cyanophenyl)-4-methoxy-1-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]acetate(80.0 mg, 164 μmol) in tetrahydrofuran (3.2 ml, 39 mmol) was treatedwith chloro(methyl)magnesium (190 μl, 3.0 M in tetrahydrofuran, 580μmol) at 0° C. The mixture was stirred overnight at ambient temperature.The mixture was diluted with potassium sodium tartrate solution andwater and extracted with ethyl acetate. The organic phase was dried overmagnesium sulfate and concentrated under reduced pressure. The crudeproduct was purified by flash-chromatography for two times (column: SNAPUltra 10 g, solvent: 100% dichloromethane to 6% methanol/dichloromethaneand column: KP-Sil 10 g, solvent: ethyl acetate/cyclohexane 1:1 to ethylacetate) to yield 9.20 mg (10%) of the desired product.

LC-MS (method 10): R_(t)=1.80 min; MS (ESIpos): m/z=473 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (0.63), 0.007(0.42), 1.090 (11.74), 1.161 (1.34), 1.175 (2.65), 1.190 (1.32), 1.989(4.62), 2.146 (0.78), 2.169 (2.30), 2.436 (3.07), 2.584 (9.75), 3.578(0.46), 3.633 (0.72), 3.636 (0.63), 3.652 (6.64), 3.729 (16.00), 3.750(0.49), 4.023 (1.04), 4.037 (1.04), 4.241 (3.29), 7.870 (2.95), 7.874(1.19), 7.884 (1.35), 7.888 (3.53), 8.035 (3.19), 8.039 (1.16), 8.052(2.44), 8.482 (0.98), 9.463 (1.25).

Example 4291-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-ol

A microwave vial was charged with1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-ol (75.0 mg, 334μmol) and1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine(100 mg, 90% purity, 367 μmol) and the contents were suspended in1,4-dioxane (1.1 mL). The reaction mixture was degassed with Ar for 3min. Tris(dibenzylideneacetone)dipalladium (6.11 mg, 6.68 μmol) andXantPhos (7.73 mg, 13.4 μmol) were added and the reaction mixture wasdegassed again for 1 min. Finally, sodium phenolate (42.6 mg, 367 μmol)was added and the vial was sealed and heated at 85° C. overnight whilevigorously shaking. After cooling to ambient temperature, the reactionmixture was diluted with ethyl acetate and filtered. The filtrate waswashed with brine, dried over sodium sulfate and concentrated. Theresidue was purified by flash column chromatography (SNAP Ultra 25 g,cyclohexane/ethyl acetate gradient) and further by preparative HPLC(column: Chromatorex C18; 125*30 mm, 10 μM, flow 75 mL/min, gradientacetonitrile/water (containing 0.1% trifluoroacetic acid) 10/90 to 95/5)to yield the desired product (5.5 mg, 4% yield).

LC-MS (method 10): R_(t)=1.87 min; MS (ESIpos): m/z=434 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.291 (2.45), 0.300(2.53), 0.420 (2.42), 0.436 (2.50), 1.183 (0.79), 1.193 (1.06), 1.233(0.35), 1.412 (0.29), 1.649 (0.64), 1.983 (0.58), 2.002 (12.79), 2.073(0.64), 2.106 (2.92), 2.515 (16.00), 3.820 (2.47), 3.833 (2.38), 7.110(0.18), 7.255 (1.95), 7.273 (3.96), 7.290 (2.20), 7.717 (1.43), 7.730(2.01), 7.745 (1.43), 8.403 (0.76), 9.270 (0.96).

Example 430N-{1-(cyclopropylmethyl)-3-[4-fluoro-3-(methylsulfanyl)phenyl]-4-methyl-1H-pyrazol-5-yl}-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

This compound was obtained as a by-product during the synthesis ofN-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-[3,5-dimethyl-4-(methylsulfanyl)-1H-pyrazol-1-yl]pyrimidin-4-amine.It was purified by preparative HPLC (column: Chromatorex C18; 125*30 mm,10 μM, flow 100 mL/min, gradient acetonitrile/water (containing 0.1%trifluoroacetic acid) 10/90 to 90/10) to yield the title compound (10mg, 5% yield).

LC-MS (method 11): R_(t)=1.58 min; MS (ESIpos): m/z=464 [M+H]⁺

¹H-NMR (600 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.319 (2.53), 0.326(2.55), 0.449 (2.57), 0.462 (2.60), 1.205 (0.41), 1.213 (0.73), 1.218(0.73), 1.225 (1.01), 1.233 (0.72), 1.238 (0.74), 1.249 (0.77), 2.033(0.72), 2.046 (11.47), 2.154 (7.62), 2.191 (2.64), 2.241 (0.60), 2.249(0.92), 2.272 (0.69), 2.558 (16.00), 2.650 (12.22), 3.863 (2.24), 3.874(2.26), 4.133 (0.87), 6.155 (2.27), 7.279 (1.07), 7.295 (1.75), 7.310(1.28), 7.541 (0.92), 7.614 (1.12), 7.625 (1.20), 8.485 (0.63), 9.398(0.59).

Example 431 tert-butyl1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate

In a sealed microwave tube under argon,1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine(60.0 mg, 245 μmol), tert-butyl1-(6-chloropyrimidin-4-yl)-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate(86.6 mg, 269 μmol), sodium phenolate (31.2 mg, 269 μmol),tris(dibenzylidenaceton)dipalladium (6.72 mg, 7.34 μmol), Xantphos (7.76mg, 14.7 μmol) were dissolved in 1,4-dioxane (1.2 ml). The reactionmixture was heated at 90° C. for 45 minutes. The cooled reaction mixturewas diluted with dichloromethane, washed with a saturated aqueoussolution of sodium hydrogen carbonate and the aqueous phase thenextracted twice with dichloromethane. The combined organic phase s weredried with sodium sulfate and concentrated in vacuo. The crude productwas purified by flash-chromatography on silica gel (Gradient 20% to 100%ethylacetate in cyclohexane, column: Biotage SNAP Ultra 10 g) and thenby preparative HPLC (method 19) to yield 78.2 mg (100% purity, 60%yield) of the desired product.

LC-MS (Method 9): R_(t)=1.26 min; MS (ESIpos): m/z=531 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.292 (1.18), 0.413(1.29), 0.429 (1.30), 1.183 (0.53), 1.230 (0.41), 1.453 (12.33), 1.468(16.00), 2.007 (10.49), 3.837 (0.96), 4.326 (0.94), 4.352 (0.78), 4.738(1.20), 4.766 (1.41), 7.257 (1.19), 7.275 (2.30), 7.292 (1.22), 7.634(0.11), 7.735 (1.10), 8.513 (0.18), 9.557 (0.19).

Example 4326-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]-N-{5-[4-(difluoromethyl)phenyl]-1,4-dimethyl-1H-pyrazol-3-yl}pyrimidin-4-amine

A microwave vial was charged4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (84.4mg, 345 μmol),5-[4-(difluoromethyl)phenyl]-1,4-dimethyl-1H-pyrazol-3-amine (90.0 mg,379 μmol) and sodium phenolate (44.0 mg, 379 μmol) and the contents weresuspended in 1,4-dioxane (1.3 ml, 15 mmol). The reaction mixture wasdegassed with Ar for 3 min. Tris(dibenzylidenaceton)dipalladium (9.47mg, 10.3 μmol) and Xantphos (12.0 mg, 20.7 μmol) were added and thereaction mixture was degassed again for 1 min. The vial was sealed andheated at 85° C. overnight while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with water andextracted with dichloromethane (2×). The combined organic phases weredried over sodium sulfate and concentrated under reduced pressure. Thecrude product was purified by preparative HPLC (method 4) and furtherflash-chromatography on silica gel to yield the desired product (65.0mg, 40%).

LC-MS (method 10): R_(t)=2.15 min; MS (ESIpos): m/z=446 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.162 (0.55), 1.176(1.11), 1.190 (0.58), 1.989 (2.08), 2.064 (16.00), 2.290 (1.51), 2.340(0.43), 3.694 (5.68), 4.024 (0.47), 4.038 (0.47), 6.789 (2.05), 6.963(1.22), 7.075 (2.56), 7.187 (1.09), 7.634 (2.52), 7.650 (2.84), 7.714(1.13), 7.822 (2.59), 7.838 (1.86), 7.853 (1.55), 7.931 (1.01), 9.639(1.13).

Example 433 tert-butyl2-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-2,6-dihydropyrrolo[3,4-c]pyrazole-5(4H)-carboxylate

In a sealed microwave tube under argon,1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine(60.0 mg, 245 μmol), tert-butyl2-(6-chloropyrimidin-4-yl)-2,6-dihydropyrrolo[3,4-c]pyrazole-5(4H)-carboxylate(86.6 mg, 269 μmol), sodium phenolate (31.2 mg, 269 μmol),tris(dibenzylidenaceton)dipalladium (6.72 mg, 7.34 μmol), Xantphos (7.76mg, 14.7 μmol) were dissolved in 1,4-dioxane (1.2 ml). The reactionmixture was heated at 90° C. for 45 minutes. The cooled reaction mixturewas diluted with dichloromethane, washed with a saturated aqueoussolution of sodium hydrogen carbonate and the aqueous phase thenextracted twice with dichloromethane. The combined organic phase s weredried with sodium sulfate and concentrated in vacuo. The crude productwas purified by flash-chromatography on silica gel (Gradient 20% to 100%ethylacetate in cyclohexane, column: Biotage SNAP Ultra 10 g) and thenby preparative HPLC (method 19) to yield 80.2 mg (100% purity, 62%yield) of the desired product.

LC-MS (Method 9): R_(t)=1.24 min; MS (ESIpos): m/z=531 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.009 (0.72), 0.290(1.47), 0.411 (1.63), 0.426 (1.65), 1.159 (0.52), 1.173 (0.99), 1.181(0.73), 1.187 (0.75), 1.230 (0.69), 1.448 (16.00), 1.514 (0.53), 1.987(0.91), 2.011 (6.91), 2.015 (6.96), 3.835 (1.42), 4.370 (1.42), 4.393(1.70), 7.259 (1.44), 7.276 (2.81), 7.294 (1.50), 7.740 (1.27), 8.377(1.64), 8.396 (1.30), 8.501 (0.22), 9.546 (0.24).

Example 434N-[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged with4-chloro-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (100 mg,100% purity, 419 μmol) and5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-amine (94.6 mg, 461 μmol)and the contents were suspended in 1,4-dioxane (1.3 mL). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (11.5 mg, 12.6 μmol) and XantPhos(14.5 mg, 25.1 μmol) were added and the reaction mixture was degassedagain for 1 min. Finally, sodium phenolate (53.5 mg, 461 μmol) was addedand the vial was sealed and heated at 85° C. overnight while vigorouslyshaking. After cooling to ambient temperature, the reaction mixture wasdiluted with dimethylsulfoxide, filtered and purified by preparativeHPLC (method 3) to yield the desired product (92 mg, 53% yield).

LC-MS (method 9): R_(t)=1.10 min; MS (ESIpos): m/z=408 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.847 (8.63), 2.194(10.48), 3.687 (11.28), 3.703 (16.00), 7.355 (1.03), 7.361 (1.77), 7.365(0.71), 7.374 (0.92), 7.379 (3.13), 7.383 (0.83), 7.392 (0.75), 7.397(1.85), 7.512 (1.70), 7.516 (0.72), 7.523 (1.87), 7.529 (1.49), 7.536(0.61), 7.540 (1.30), 8.429 (2.21), 9.366 (1.70).

Example 4354-(3-{[6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-1,4-dimethyl-1H-pyrazol-5-yl)benzonitrile

A microwave vial was charged with4-chloro-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (100 mg,100% purity, 419 μmol) and4-(3-amino-1,4-dimethyl-1H-pyrazol-5-yl)benzonitrile (97.8 mg, 461μmol), and the contents were suspended in 1,4-dioxane (1.3 mL). Thereaction mixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (11.5 mg, 12.6 μmol) and XantPhos(14.5 mg, 25.1 μmol) were added and the reaction mixture was degassedagain for 1 min. Finally, sodium phenolate (53.5 mg, 461 μmol) wasadded, the vial was sealed and heated at 85° C. overnight whilevigorously shaking. After cooling to ambient temperature, the reactionmixture was diluted with dimethylsulfoxide, filtered and purified bypreparative HPLC (method 3) to yield the desired product (108 mg, 55%yield).

LC-MS (method 9): R_(t)=1.02 min; MS (ESIpos): m/z=415 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (0.41), 1.647(0.60), 1.882 (7.84), 2.195 (9.66), 2.212 (0.48), 2.558 (0.54), 3.703(16.00), 3.713 (0.75), 3.735 (10.38), 7.359 (0.80), 7.370 (0.53), 7.384(0.48), 7.394 (0.48), 7.698 (2.65), 7.702 (0.94), 7.711 (1.03), 7.715(2.90), 8.004 (3.01), 8.008 (0.97), 8.018 (0.97), 8.021 (2.67), 8.433(1.91), 8.434 (1.90), 9.412 (1.50).

Example 4364-(5-{[6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-1,4-dimethyl-1H-pyrazol-3-yl)benzonitrile

A microwave vial was charged with4-chloro-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (100 mg,100% purity, 419 μmol) and4-(5-amino-1,4-dimethyl-1H-pyrazol-3-yl)benzonitrile (97.8 mg, 461μmol), and the contents were suspended in 1,4-dioxane (1.3 mL). Thereaction mixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (11.5 mg, 12.6 μmol) and XantPhos(14.5 mg, 25.1 μmol) were added and the reaction mixture was degassedagain for 1 min. Finally, sodium phenolate (53.5 mg, 461 μmol) was addedand the vial was sealed and heated at 85° C. overnight while vigorouslyshaking. After cooling to ambient temperature, the reaction mixture wasdiluted with dimethylsulfoxide, filtered and purified by preparativeHPLC (method 3) to yield the desired product (78 mg, 43% yield).

LC-MS (method 9): R_(t)=1.05 min; MS (ESIpos): m/z=415 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (0.40), 0.006(0.28), 1.526 (0.23), 1.647 (0.59), 2.068 (16.00), 2.187 (2.54), 3.691(9.61), 3.702 (10.96), 7.371 (0.39), 7.385 (0.42), 7.395 (0.45), 7.896(14.92), 7.914 (0.37), 8.454 (0.70), 9.444 (1.66).

Example 437N-[3-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-5-yl]-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged with4-chloro-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (100 mg,100% purity, 419 μmol) and3-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-5-amine (94.6 mg, 461 μmol),and the contents were suspended in 1,4-dioxane (1.3 mL). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (11.5 mg, 12.6 μmol) and XantPhos(14.5 mg, 25.1 μmol) were added and the reaction mixture was degassedagain for 1 min. Finally, sodium phenolate (53.5 mg, 461 μmol) was addedand the vial was sealed and heated at 85° C. overnight while vigorouslyshaking. After cooling to ambient temperature, the reaction mixture wasfiltered and concentrated. The residue was redissolved indimethylsulfoxide and purified by preparative HPLC (method 3) to yieldthe desired product (67 mg, 38% yield).

LC-MS (method 9): R_(t)=1.09 min; MS (ESIpos): m/z=408 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (0.42), 2.012(16.00), 2.183 (2.57), 3.655 (9.20), 3.700 (10.51), 7.249 (1.97), 7.253(0.76), 7.267 (3.93), 7.284 (2.05), 7.700 (1.36), 7.711 (1.66), 7.717(1.59), 7.728 (1.20), 8.454 (0.68), 9.393 (1.60).

Example 438 ethyl1-(6-{[1-(cyclopropylmethyl)-3-(5-fluoropyridin-2-yl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

A microwave vial was charged ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (117mg, 415 μmol) and1-(cyclopropylmethyl)-3-(5-fluoropyridin-2-yl)-4-methyl-1H-pyrazol-5-amine (225 mg, 50% purity, 457 μmol) and the contents weresuspended in 1,4-dioxane (1.6 ml, 19 mmol). The reaction mixture wasdegassed with Ar for 3 min. Tris(dibenzylidenaceton)dipalladium (11.4mg, 12.5 μmol) and Xantphos (14.4 mg, 24.9 μmol) were added and thereaction mixture was degassed again for 1 min and heated to 85° C. Atthis temperature and sodium phenolate (53.0 mg, 457 μmol) was added. Thevial was sealed and heated at 85° C. for 90 minutes while vigorouslystirred. After cooling to ambient temperature, the reaction mixture wasfiltered and preparative HPLC (method: column: Reprosil C18; 10 μm;125×30 mm/flow: 50 mL/min/solvent: A=water (0.01% formic acid),B=acetonitrile/grradient: 0.00-5.00 min=10% B, 6.50 min=20% B,17.0-19.75 min=100% B, 19.75-23.00 min=90% B) and further byflash-chromatography (column: SNAP KP-Sil 10 g, solvent: 96%dichloromethane/4% ethyl acetate to 66% dichloromethane/34% ethylacetate to 50% dichloromethane/50% ethyl acetate) to yield the desiredproduct (62.7 mg, 31%).

LC-MS (method 10): R_(t)=2.34 min; MS (ESIpos): m/z=491 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (0.53), 0.314(2.05), 0.323 (2.09), 0.442 (2.26), 0.458 (2.30), 1.177 (0.42), 1.191(0.52), 1.201 (0.69), 1.207 (0.67), 1.217 (1.04), 1.226 (0.75), 1.231(0.74), 1.242 (0.49), 1.289 (2.49), 1.303 (4.64), 1.317 (2.39), 1.991(0.54), 2.156 (16.00), 2.368 (1.64), 2.909 (10.82), 3.867 (1.47), 3.878(1.44), 4.230 (0.81), 4.244 (2.14), 4.258 (2.12), 4.272 (0.78), 7.754(0.60), 7.760 (0.67), 7.772 (1.27), 7.778 (1.37), 7.789 (0.75), 7.795(0.77), 7.991 (0.73), 8.000 (0.83), 8.008 (0.76), 8.017 (0.66), 8.592(2.63), 8.598 (2.64).

Example 4396-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-[1-(cyclopropylmethyl)-3-(5-fluoropyridin-2-yl)-4-methyl-1H-pyrazol-5-yl]pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (101 mg,415 μmol) and1-(cyclopropylmethyl)-3-(5-fluoropyridin-2-yl)-4-methyl-1H-pyrazol-5-amine(225 mg, 50% purity, 457 μmol) and the contents were suspended in1,4-dioxane (1.6 ml, 19 mmol). The reaction mixture was degassed with Arfor 3 min. Tris(dibenzylidenaceton)dipalladium (11.4 mg, 12.5 μmol) andXantphos (14.4 mg, 24.9 μmol) were added and the reaction mixture wasdegassed again for 1 min and heated to 85° C. At this temperature andsodium phenolate (53.0 mg, 457 μmol) was added. The vial was sealed andheated at 85° C. for 90 minutes while vigorously stirred. After coolingto ambient temperature, the reaction mixture was filtered and purifiedby preparative HPLC (method: column: Reprosil C18; 10 μm; 125×30mm/flow: 50 mL/min/solvent: A=water (0.01% formic acid),B=acetonitrile/grradient: 0.00-5.00 min=10% B, 6.50 min=20% B,17.0-19.75 min=100% B, 19.75-23.00 min=90% B) and further byflash-chromatography (column: SNAP KP-Sil 10 g, solvent: 96%dichloromethane/4% ethyl acetate to 66% dichloromethane/34% ethylacetate to 55% dichloromethane/45% ethyl acetate) to yield the desiredproduct (50.6 mg, 27%).

LC-MS (method 10): R_(t)=2.50 min; MS (ESIpos): m/z=453 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.310 (1.78), 0.319(1.78), 0.438 (1.97), 0.454 (1.95), 1.079 (0.58), 1.093 (1.17), 1.107(0.59), 1.163 (1.91), 1.178 (3.84), 1.192 (2.15), 1.196 (0.64), 1.202(0.59), 1.212 (0.83), 1.221 (0.54), 1.226 (0.55), 1.991 (7.07), 2.153(14.26), 2.199 (1.13), 2.645 (16.00), 3.378 (0.58), 3.391 (0.57), 3.571(1.75), 3.866 (1.40), 3.877 (1.35), 4.011 (0.58), 4.026 (1.66), 4.040(1.64), 4.054 (0.55), 7.755 (0.52), 7.761 (0.57), 7.773 (1.06), 7.779(1.10), 7.790 (0.61), 7.796 (0.60), 7.995 (0.67), 8.003 (0.75), 8.011(0.68), 8.020 (0.57), 8.593 (2.14), 8.599 (2.08).

Example 440 propan-2-yl[1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]acetate

Under an argon atmosphere a Schlenk tube was charged with a ethyl[1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]acetate(235 mg, 90% purity, 443 μmol) in tetrahydrofuran (2.0 ml, 25 mmol).Titanium isopropoxylate (140 μl, 490 μmol) and ethylmagnesium bromide(1.6 ml, 1.0 M in tetrahydrofuran, 1.6 mmol) were added at 0° C. Themixture was stirred 2 hours at 0° C. and overnight at ambienttemperature. The mixture was diluted with saturated ammonium chloridesolution. The occurring precipitate was filtered off. The filtrate wasextracted with ethyl acetate (3×). The combined organic phases werewashed with brine, dried over sodium sulfate and concentrated underreduced pressure. The crude product was purified by preparative HPLC(method: column: Reprosil C18; 10 μm; 125×40 mm/flow: 75 mL/min/solvent:A=water (0.1% formic acid), B=acetonitrile/grradient: 0.00-5.50 min=10%B, 17.65-19.48 min=95% B, 19.66 min=10% B) to yield 85.0 mg (39%) of thedescribed by-product along with the desired product1-{[1-(6-{[4-ethyl-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]methyl}cyclopropanol.

LC-MS (method 10): R_(t)=2.31 min; MS (ESIpos): m/z=492 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.006 (0.48), 0.874(2.95), 0.889 (6.35), 0.904 (2.94), 1.091 (0.55), 1.180 (16.00), 1.192(15.88), 2.145 (11.95), 2.289 (0.74), 2.304 (2.08), 2.319 (2.01), 2.334(0.65), 2.571 (12.11), 3.312 (14.32), 3.435 (6.49), 4.862 (0.45), 4.875(1.13), 4.887 (1.51), 4.900 (1.11), 4.912 (0.43), 7.329 (1.88), 7.361(1.66), 7.379 (3.55), 7.396 (2.02), 7.503 (2.05), 7.507 (1.04), 7.514(2.33), 7.520 (1.92), 7.531 (1.57), 8.446 (2.96), 9.335 (1.91).

Example 4414-[4-chloro-1-(cyclopropylmethyl)-5-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-1H-pyrazol-3-yl]benzonitrile

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (100 mg, 479 μmol),4-[5-amino-4-chloro-1-(cyclopropylmethyl)-1H-pyrazol-3-yl]benzonitrile(144 mg, 527 μmol) and sodium phenolate (61.2 mg, 527 μmol) and thecontents were suspended in 1,4-dioxane (2.2 ml, 26 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (5.71 mg, 6.23 μmol) and Xantphos(8.32 mg, 14.4 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with water and extracted with ethyl acetate(2×). The combined organic phases were washed with water and brine,dried over sodium sulfate and concentrated under reduced pressure. Thecrude product was purified by preparative HPLC (method: column: ReprosilC18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent: A=water (0.1% formicacid), B=acetonitrile/grradient: 0.00-4.25 min=20% B, 4.50 min=30% B,19.00-22.50 min=100% B, 22.75-25.00 min=20% B) to yield the desiredproduct (33.1 mg, 16%).

LC-MS (method 10): R_(t)=2.32 min; MS (ESIpos): m/z=445 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (2.40), 0.008(2.44), 0.326 (0.76), 0.338 (3.16), 0.352 (3.42), 0.363 (1.12), 0.458(0.95), 0.468 (2.73), 0.472 (2.70), 0.488 (2.93), 0.504 (0.66), 1.210(0.43), 1.223 (0.72), 1.242 (1.15), 1.261 (0.69), 2.187 (9.98), 2.328(0.82), 2.636 (16.00), 2.670 (0.92), 3.930 (3.79), 3.948 (3.79), 6.163(4.02), 7.952 (4.51), 7.973 (6.68), 8.086 (5.99), 8.107 (4.48), 8.489(2.27), 9.693 (2.24).

Example 442 ethyl1-(6-{[4-chloro-3-(4-cyanophenyl)-1-(cyclopropylmethyl)-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

A microwave vial was charged ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (250mg, 891 μmol),4-[5-amino-4-chloro-1-(cyclopropylmethyl)-1H-pyrazol-3-yl]benzonitrile(267 mg, 980 μmol) and sodium phenolate (114 mg, 980 μmol) and thecontents were suspended in 1,4-dioxane (4.2 ml, 49 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (10.6 mg, 11.6 μmol) and Xantphos(15.5 mg, 26.7 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with water and extracted with ethyl acetate(2×). The combined organic phases were washed with water and brine,dried over sodium sulfate and concentrated under reduced pressure. Thecrude product was purified by preparative HPLC (method: column: ReprosilC18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent: A=water (0.1% formicacid), B=acetonitrile/grradient: 0.00-4.25 min=20% B, 4.50 min=30% B,19.00-22.50 min=100% B, 22.75-25.00 min=20% B) to yield the desiredproduct (62.5 mg, 13%).

LC-MS (method 10): R_(t)=2.42 min; MS (ESIpos): m/z=517 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.71), 0.008(1.01), 0.330 (0.78), 0.341 (2.73), 0.355 (2.76), 0.367 (0.86), 0.461(0.95), 0.472 (2.39), 0.475 (2.21), 0.492 (2.47), 0.507 (0.53), 1.091(0.44), 1.227 (0.72), 1.234 (0.87), 1.246 (1.04), 1.258 (0.68), 1.265(0.74), 1.292 (4.88), 1.298 (1.49), 1.310 (9.90), 1.316 (2.18), 1.327(4.72), 1.334 (0.98), 1.356 (0.53), 2.388 (7.78), 2.418 (2.38), 2.920(16.00), 2.933 (1.59), 2.950 (2.27), 3.936 (2.92), 3.953 (2.79), 4.234(1.40), 4.252 (4.20), 4.270 (4.20), 4.287 (1.41), 7.951 (3.92), 7.956(1.68), 7.968 (2.14), 7.973 (5.53), 7.999 (0.43), 8.002 (0.42), 8.083(5.13), 8.087 (1.90), 8.104 (3.66), 8.570 (1.54), 9.858 (1.29).

Example 4434-(3-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-4-methoxy-1-methyl-1H-pyrazol-5-yl)benzonitrile

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (499 mg, 2.39 mmol)and 4-(3-amino-4-methoxy-1-methyl-1H-pyrazol-5-yl)benzonitrile (600 mg,2.63 mmol) and the contents were suspended in 1,4-dioxane (19 ml, 220mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (65.6 mg, 71.7 μmol) and Xantphos(83.0 mg, 143 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (305 mg, 2.63 mmol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with hydrochloricacid and extracted with ethyl acetate (2×). The combined organic phaseswere washed with water and brine, dried over sodium sulfate andconcentrated under reduced pressure. The crude product was purified byflash-chromatography (column: SNAP Ultra 25 g, solvent:dichloromethane/ethyl acetate 1:1) to yield the desired product (630 mg,65%).

LC-MS (method 10): R_(t)=1.82 min; MS (ESIpos): m/z=401 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.016 (1.05), 2.159(4.70), 2.522 (16.00), 3.292 (2.94), 3.525 (4.97), 3.548 (5.33), 3.766(5.36), 6.115 (1.41), 7.183 (1.50), 7.752 (2.91), 7.983 (3.21), 8.435(1.57), 9.403 (1.42).

Example 4444-(5-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-4-methoxy-1-methyl-1H-pyrazol-3-yl)benzonitrile

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (83.1 mg, 398 μmol)and 4-(5-amino-4-methoxy-1-methyl-1H-pyrazol-3-yl)benzonitrile (100 mg,438 μmol) and the contents were suspended in 1,4-dioxane (2.8 ml, 33mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (4.74 mg, 5.18 μmol) and Xantphos(6.91 mg, 11.9 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (50.9 mg, 438 μmol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was filtered and purified bypreparative HPLC (method 7) to yield the desired product (43.0 mg, 27%).

LC-MS (method 9): R_(t)=1.01 min; MS (ESIpos): m/z=401 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.62), 0.008(0.68), 2.178 (3.94), 2.637 (9.70), 3.652 (8.39), 3.729 (16.00), 6.157(2.40), 7.870 (2.84), 7.891 (3.85), 8.033 (3.50), 8.055 (2.73), 8.498(1.40), 9.516 (1.65).

Example 4454-[4-chloro-1-(cyclopropylmethyl)-5-({6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-yl}amino)-1H-pyrazol-3-yl]benzonitrile

A microwave vial was charged4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (100mg, 409 μmol),4-[5-amino-4-chloro-1-(cyclopropylmethyl)-1H-pyrazol-3-yl]benzonitrile(123 mg, 450 μmol) and sodium phenolate (52.2 mg, 450 μmol) and thecontents were suspended in 1,4-dioxane (1.9 ml, 22 mmol). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (4.87 mg, 5.31 μmol) and Xantphos(7.10 mg, 12.3 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was diluted with water and extracted with ethyl acetate(2×). The combined organic phases were washed with water and brine,dried over sodium sulfate and concentrated under reduced pressure. Thecrude product was purified by preparative HPLC (method: column: ReprosilC18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent: A=water (0.01% formicacid), B=acetonitrile/grradient: 0.00-5.00 min=10% B, 6.50 min=20% B,17.0-19.75 min=100% B, 19.75-23.00 min=90% B) to yield the desiredproduct (34.7 mg, 18%).

LC-MS (method 11): R_(t)=1.55 min; MS (ESIpos): m/z=481 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.95), −0.007(9.69), 0.146 (0.97), 0.325 (1.72), 0.337 (7.15), 0.350 (7.92), 0.362(2.38), 0.458 (2.10), 0.468 (6.41), 0.471 (6.23), 0.488 (6.92), 0.503(1.46), 1.210 (0.90), 1.222 (1.74), 1.230 (1.74), 1.241 (2.64), 1.253(1.59), 1.260 (1.62), 2.073 (0.95), 2.298 (16.00), 2.328 (1.36), 2.670(1.00), 2.708 (1.10), 3.939 (7.33), 3.957 (7.23), 5.754 (1.97), 6.804(9.15), 7.679 (3.23), 7.815 (6.62), 7.954 (10.97), 7.976 (14.00), 8.087(11.85), 8.108 (8.77), 8.528 (3.46), 9.875 (2.79).

Example 446 ethyl1-(6-{[3-(4-cyanophenyl)-4-methoxy-1-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

A microwave vial was charged ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (215mg, 766 μmol) and4-(5-amino-4-methoxy-1-methyl-1H-pyrazol-3-yl)benzonitrile (192 mg, 842μmol) and the contents were suspended in 1,4-dioxane (6.8 ml, 80 mmol).The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (9.12 mg, 9.96 μmol) and Xantphos(13.3 mg, 23.0 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (97.8 mg, 842 μmol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with hydrochloricacid and extracted with ethyl acetate (2×). The combined organic phaseswere dried over Extrelut NT3 and concentrated under reduced pressure.The crude product was recrystallized from acetonitrile to yield thedesired product (167 mg, 46%).

LC-MS (method 10): R_(t)=2.11 min; MS (ESIpos): m/z=473 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.290 (3.15), 1.308(6.39), 1.325 (3.21), 2.378 (3.97), 2.919 (11.28), 3.633 (0.43), 3.657(8.77), 3.728 (16.00), 4.231 (0.99), 4.249 (2.89), 4.267 (2.86), 4.284(0.96), 7.870 (3.05), 7.891 (3.80), 8.029 (3.92), 8.050 (3.00), 8.575(1.21), 9.684 (1.29).

Example 447 ethyl1-(6-{[4-chloro-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate

A microwave vial was charged with4-chloro-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (200 mg, 886μmol) and sodium phenolate (103 mg, 886 μmol) and the contents weresuspended in 1,4-dioxane (1.9 mL). The reaction mixture was degassedwith Ar for 3 min. ethyl1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate (239 mg,90% purity, 806 μmol), Tris(dibenzylideneacetone)dipalladium (9.59 mg,10.5 μmol) and XantPhos (14.0 mg, 24.2 μmol) were added and the reactionmixture was degassed again for 1 min. The vial was sealed and heated at90° C. overnight while vigorously shaking. After cooling to ambienttemperature, the reaction mixture was loaded onto silica gel andpurified by flash column chromatography (SNAP Ultra 25 g,cyclohexane/ethyl acetate gradient 95/5 to 20/80) to yield the desiredproduct (124 mg, 30% yield).

LC-MS (method 10): R_(t)=2.10 min; MS (ESIpos): m/z=456 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.90), 0.008(1.07), 1.157 (0.44), 1.175 (0.90), 1.198 (4.38), 1.215 (9.45), 1.226(0.72), 1.233 (4.65), 1.292 (0.45), 1.310 (0.94), 1.328 (0.45), 1.398(4.08), 1.989 (1.59), 2.278 (12.99), 2.685 (1.10), 3.740 (0.45), 3.776(16.00), 4.243 (1.35), 4.260 (4.35), 4.278 (4.33), 4.296 (1.37), 4.305(0.49), 4.322 (0.42), 6.761 (4.57), 7.155 (3.16), 7.157 (3.26), 7.410(1.98), 7.415 (0.74), 7.432 (4.32), 7.449 (0.81), 7.454 (2.41), 7.634(2.41), 7.639 (1.07), 7.647 (2.64), 7.656 (2.31), 7.664 (0.88), 7.669(2.01), 8.443 (2.84), 9.769 (2.35).

Example 448 ethyl4-chloro-1-(6-{[4-chloro-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate

A microwave vial was charged with4-chloro-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-amine (200 mg, 886μmol) and sodium phenolate (103 mg, 886 μmol) and the contents weresuspended in 1,4-dioxane (1.9 mL). The reaction mixture was degassedwith Ar for 3 min. ethyl4-chloro-1-(6-chloropyrimidin-4-yl)-3-methyl-1H-pyrazole-5-carboxylate(324 mg, 75% purity, 806 μmol), tris(dibenzylideneacetone)dipalladium(9.59 mg, 10.5 μmol) and XantPhos (14.0 mg, 24.2 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously shaking. After coolingto ambient temperature, the reaction mixture was loaded onto silica geland purified by flash column chromatography (SNAP Ultra 25 g,cyclohexane/ethyl acetate 95/5 to 20/80) to yield the desired product(154 mg, 33% yield).

LC-MS (method 10): R_(t)=2.35 min; MS (ESIpos): m/z=490 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.29), 0.008(1.55), 1.157 (1.51), 1.175 (3.02), 1.193 (1.53), 1.237 (7.34), 1.245(1.40), 1.255 (15.51), 1.272 (7.41), 1.304 (0.50), 1.321 (0.86), 1.338(0.51), 1.398 (13.21), 1.989 (5.51), 2.287 (10.21), 2.329 (0.43), 2.671(0.41), 2.675 (0.44), 2.687 (3.42), 3.738 (16.00), 3.779 (1.22), 4.003(0.43), 4.021 (1.30), 4.039 (1.29), 4.056 (0.43), 4.336 (2.40), 4.342(0.73), 4.354 (7.54), 4.371 (7.47), 4.389 (2.37), 7.303 (3.64), 7.325(7.42), 7.347 (3.94), 7.433 (0.41), 7.873 (0.93), 7.881 (3.00), 7.886(2.11), 7.895 (3.79), 7.903 (3.38), 7.912 (1.48), 7.917 (2.74), 8.479(2.28), 9.965 (2.57).

Example 449 ethyl1-(6-{[4-chloro-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

A microwave vial was charged with4-chloro-3-(4-fluorophenyl)-1-methyl-1H-pyrazol-5-amine (200 mg, 886μmol) and sodium phenolate (103 mg, 886 μmol) and the contents weresuspended in 1,4-dioxane (1.9 mL). The reaction mixture was degassedwith Ar for 3 min. ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (226mg, 806 μmol), tris(dibenzylideneacetone)dipalladium (9.59 mg, 10.5μmol) and XantPhos (14.0 mg, 24.2 μmol) were added and the reactionmixture was degassed again for 1 min. The vial was sealed and heated at85° C. overnight while vigorously shaking. After cooling to ambienttemperature, the reaction mixture was loaded onto silica gel andpurified by flash column chromatography (cyclohexane/ethyl acetate 95/5to 20/80) to yield the desired product (185 mg, 49% yield).

LC-MS (method 10): R_(t)=2.33 min; MS (ESIpos): m/z=470 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.80), 0.008(0.53), 1.158 (0.62), 1.175 (1.23), 1.193 (0.63), 1.293 (4.71), 1.311(9.76), 1.328 (4.65), 1.398 (0.91), 1.989 (2.04), 2.390 (7.85), 2.471(0.70), 2.899 (1.16), 2.919 (16.00), 3.734 (11.85), 3.772 (0.86), 4.021(0.48), 4.039 (0.47), 4.235 (1.40), 4.253 (4.11), 4.271 (4.01), 4.288(1.24), 7.302 (2.49), 7.307 (1.00), 7.319 (1.23), 7.324 (4.66), 7.341(0.93), 7.346 (2.47), 7.878 (2.22), 7.883 (1.13), 7.891 (2.46), 7.900(2.36), 7.908 (0.98), 7.914 (2.00), 8.580 (1.65), 9.863 (2.55).

Example 450N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methoxy-1H-pyrazol-5-yl]-6-[3,5-dimethyl-4-(5-methyl-1,3,4-oxadiazol-2-yl)-1H-pyrazol-1-yl]pyrimidin-4-amine

A solution ofN′-acetyl-1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methoxy-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbohydrazide(250 mg, 469 μmol) in tetrahydrofuran (10 ml, 120 mmol) was treated withBurgess reagent (223 mg, 937 μmol) and stirred over the weekend atambient temperature. The mixture was purified by preparative HPLC(method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent:A=water (0.01% formic acid), B=acetonitrile/grradient: 0.00-5.00 min=10%B, 6.50 min=20% B, 17.0-19.75 min=100% B, 19.75-23.00 min=90% B) toyield 168 mg (69%) of the desired product.

LC-MS (method 10): R_(t)=2.03 min; MS (ESIpos): m/z=516 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.296 (0.62), 0.309(2.92), 0.322 (3.24), 0.334 (0.94), 0.439 (0.85), 0.450 (2.39), 0.453(2.37), 0.470 (2.58), 0.485 (0.68), 1.189 (0.62), 1.196 (0.60), 1.208(0.91), 1.220 (0.58), 1.227 (0.61), 2.571 (13.24), 2.976 (13.06), 3.693(16.00), 3.782 (2.06), 3.799 (2.05), 7.248 (1.93), 7.270 (3.86), 7.292(2.07), 7.886 (1.75), 7.900 (2.16), 7.907 (2.11), 7.921 (1.68), 8.578(0.83), 9.614 (0.55).

Example 4514-(4-{[6-(4-acetyl-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-3,5-dimethyl-1H-pyrazol-1-yl)benzonitrile

A microwave vial was charged1-[1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]ethanone (250mg, 997 μmol) and 4-(4-amino-3,5-dimethyl-1H-pyrazol-1-yl)benzonitrile(274 mg, 85% purity, 1.10 mmol) and the contents were suspended in1,4-dioxane (4.0 ml, 47 mmol). The reaction mixture was degassed with Arfor 3 min. Tris(dibenzylidenaceton)dipalladium (27.4 mg, 29.9 μmol) andXantphos (34.6 mg, 59.8 μmol) were added and the reaction mixture wasdegassed again for 1 min and heated to 85° C. At this temperature andsodium phenolate (127 mg, 1.10 mmol) was added. The vial was sealed andheated at 85° C. for 90 minutes while vigorously stirring. After coolingto ambient temperature, the reaction mixture was diluted withhydrochloric acid and extracted with ethyl acetate (2×). The combinedorganic phases were washed with water and brine, dried over sodiumsulfate and concentrated under reduced pressure. The remaining residuewas suspended in acetonitrile, the occurring precipitate was collectedby filtration, washed and dried to yield 200 mg of the desired product.The filtrate was concentrated and purified by preparative HPLC (method:column: Reprosil C18; 10 μm; 125×40 mm/flow: 75 mL/min/solvent: A=water(0.1% formic acid), B=acetonitrile/grradient: 0.00-5.50 min=10% B,17.65-19.48 min=95% B, 19.66 min=10% B) to yield further 50 mg of thedesired product (total yield: 250 mg, 60%).

LC-MS (method 10): R_(t)=1.62 min; MS (ESIpos): m/z=427 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.007 (1.11), 2.114(16.00), 2.293 (14.46), 2.307 (1.33), 2.328 (0.43), 2.367 (0.61), 2.462(7.23), 2.866 (5.87), 7.806 (2.10), 7.827 (2.68), 7.979 (3.88), 8.001(3.14), 9.133 (0.93).

Example 452N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-{4-[(3-fluoroazetidin-1-yl)methyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-amine

A solution of1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbaldehyde(180 mg, 404 μmol) and 3-fluoroazetidine hydrochloride (1:1) (58.6 mg,525 μmol) in tetrahydrofuran (3.5 ml, 43 mmol) was treated with aceticacid (46 μl, 810 μmol) and stirred for one hour at ambient temperature.Subsequently, sodium triacetoxyborohydride (137 mg, 646 μmol) was addedand the mixture was stirred overnight at ambient temperature. Themixture was diluted with water (3 mL) and purified by preparative HPLC(method: column: Reprosil C18; 10 μm; 125×40 mm/flow: 75 mL/min/solvent:A=water (0.1% formic acid), B=acetonitrile/grradient: 0.00-5.50 min=10%B, 17.65-19.48 min=95% B, 19.66 min=10% B) to yield 80.0 mg (37%) of thedesired product.

LC-MS (method 10): R_(t)=1.44 min; MS (ESIneg): m/z=503 [M−H]⁻

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.008 (0.65), 0.290(2.81), 0.302 (2.79), 0.420 (2.86), 0.440 (2.79), 1.164 (0.50), 1.175(0.81), 1.183 (0.86), 1.195 (1.15), 1.212 (0.67), 1.975 (1.02), 2.005(14.84), 2.180 (3.15), 2.524 (1.08), 2.637 (16.00), 3.005 (0.82), 3.028(1.01), 3.040 (0.88), 3.065 (0.87), 3.082 (1.01), 3.437 (5.46), 3.470(1.74), 3.485 (1.29), 3.507 (0.80), 3.823 (2.60), 3.840 (2.39), 5.026(0.55), 5.039 (0.74), 5.052 (0.50), 5.170 (0.54), 5.183 (0.74), 5.196(0.49), 7.251 (2.54), 7.273 (4.83), 7.296 (2.50), 7.713 (1.85), 7.727(2.30), 7.748 (1.49), 8.138 (1.60), 8.457 (0.73), 9.363 (0.77).

Example 453 ethyl1-(6-{[1-(4-fluorophenyl)-3,5-dimethyl-1H-pyrazol-4-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

A microwave vial was charged ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (301mg, 1.07 mmol), 1-(4-fluorophenyl)-3,5-dimethyl-1H-pyrazol-4-amine (285mg, 85% purity, 1.18 mmol) and sodium phenolate (137 mg, 1.18 mmol) andthe contents were suspended in 1,4-dioxane (5.2 ml, 61 mmol). Thereaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (12.8 mg, 13.9 μmol) and Xantphos(18.6 mg, 32.2 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was sealed and heated at 85° C. overnightwhile vigorously stirring. After cooling to ambient temperature, thereaction mixture was filtered and purified by preparative HPLC (method:column: Reprosil C18; 10 μm; 125×40 mm/flow: 75 mL/min/solvent: A=water(0.1% formic acid), B=acetonitrile/grradient: 0.00-5.50 min=10% B,17.65-19.48 min=95% B, 19.66 min=10% B) to yield the desired product(150 mg, 31%).

LC-MS (method 10): R_(t)=2.09 min; MS (ESIpos): m/z=450 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.091 (0.61), 1.285(2.43), 1.303 (4.80), 1.320 (2.48), 2.082 (16.00), 2.175 (11.93), 2.368(1.46), 2.885 (7.23), 4.224 (0.76), 4.242 (2.13), 4.259 (2.10), 4.277(0.78), 7.333 (1.46), 7.355 (3.23), 7.377 (1.87), 7.590 (1.59), 9.054(0.58).

Example 454 ethyl1-[6-({1-(cyclopropylmethyl)-3-[4-(difluoromethyl)phenyl]-4-methyl-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3,5-dimethyl-1H-pyrazole-4-carboxylate

A microwave vial was charged ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (368mg, 1.31 mmol) and1-(cyclopropylmethyl)-3-[4-(difluoromethyl)phenyl]-4-methyl-1H-pyrazol-5-amine(400 mg, 1.44 mmol) and the contents were suspended in 1,4-dioxane (5.0ml, 58 mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (36.0 mg, 39.3 μmol) and Xantphos(45.5 mg, 78.7 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (167 mg, 1.44 mmol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. The mixture was leftovernight at ambient temperature, the reaction mixture was filtered andpurified by preparative HPLC (method: column: Reprosil C18; 10 μm;125×30 mm/flow: 50 mL/min/solvent: A=water (0.01% formic acid),B=acetonitrile/grradient: 0.00-5.00 min=10% B, 6.50 min=20% B,17.0-19.75 min=100% B, 19.75-23.00 min=90% B) and further byflash-chromatography (column: SNAP KP-Sil 10 g, solvent: 92%dichloromethane/8% ethyl acetate to 34% dichloromethane/66% ethylacetate) to yield the desired product (364 mg, 53%).

LC-MS (method 10): R_(t)=2.37 min; MS (ESIpos): m/z=522 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.308 (2.61), 0.319(2.85), 0.435 (2.67), 0.455 (2.84), 1.176 (0.83), 1.183 (0.41), 1.194(0.95), 1.203 (0.73), 1.215 (1.13), 1.227 (0.70), 1.233 (0.73), 1.288(3.54), 1.305 (7.16), 1.323 (3.62), 1.990 (1.12), 2.052 (16.00), 2.373(2.15), 2.913 (13.30), 3.315 (12.00), 3.859 (2.27), 3.876 (2.23), 4.228(1.09), 4.246 (3.21), 4.264 (3.19), 4.281 (1.10), 6.938 (1.62), 7.078(3.47), 7.218 (1.46), 7.637 (3.29), 7.657 (4.07), 7.844 (3.04), 7.864(2.59), 8.540 (0.50).

Example 455N-[1-(cyclopropylmethyl)-4-methyl-3-(6-methylpyridin-3-yl)-1H-pyrazol-5-yl]-6-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidin-4-amine

In a sealed microwave tube under argon,1-(cyclopropylmethyl)-4-methyl-3-(6-methylpyridin-3-yl)-1H-pyrazol-5-amine(60.0 mg, 248 μmol),4-chloro-6-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidine(75.3 mg, 272 μmol), (31.6 mg, 272 μmol), (6.80 mg, 7.43 μmol), (7.85mg, 14.9 μmol) were dissolved in 1,4-dioxane (1.2 ml). The reactionmixture was heated at 90° C. for 30 minutes. The cooled reaction mixturewas diluted with ethylacetate, washed with a saturated aqueous solutionof sodium hydrogen carbonate and the aqueous phase then extracted twicewith ethylacetate. The combined organic phase s were dried with sodiumsulfate and concentrated in vacuo. The crude product was purified byflash-chromatography on silica gel (gradient 18% to 100% ethylacetate incyclohexane, column: Biotage SNAP Ultra 10 g) to yield 72.8 mg (100%purity, 61% yield) of the desired product.

LC-MS (Method 10): R_(t)=1.84 min; MS (ESIpos): m/z=483 [M+H]⁺

¹H-NMR (500 MHz, CHLOROFORM-d) δ [ppm]: 0.330 (0.68), 0.340 (2.77),0.351 (2.74), 0.361 (0.73), 0.555 (0.77), 0.564 (2.30), 0.566 (2.26),0.570 (1.05), 0.580 (2.37), 0.582 (2.16), 0.592 (0.59), 1.255 (0.46),1.264 (0.63), 1.271 (0.58), 1.274 (0.47), 1.280 (0.94), 1.290 (0.57),1.294 (0.55), 2.110 (16.00), 2.309 (7.02), 2.311 (6.83), 2.604 (15.69),2.804 (8.27), 2.806 (7.96), 3.946 (3.39), 3.960 (3.31), 6.599 (0.64),6.849 (0.54), 7.224 (2.11), 7.240 (2.24), 7.951 (1.75), 7.956 (1.73),7.967 (1.66), 7.972 (1.64), 8.572 (4.18), 8.574 (4.15), 8.850 (2.31),8.854 (2.22).

Example 4561-[1-(6-{[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]-3-methylbutan-1-ol

Under an argon atmosphere, ethyl1-(6-{[5-(4-fluorophenyl)-1,4-dimethyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(32.0 mg, 71.2 μmol) was dissolved in tetrahydrofuran (0.7 mL) and thesolution cooled to 0° C. Titanium isopropoxide (46 μl, 160 μmol) wasadded, followed by a solution of isobutyl magnesium chloride (250 μ, 2.0M in tetrahydrofuran, 500 μmol). The reaction mixture was stirred for 3h at 0° C. and overnight at ambient temperature. The reaction mixturewas carefully quenched by addition of aqueous saturated ammoniumchloride solution and extracted with ethyl acetate (3×). The combinedorganic phase extracts were washed with brine, dried over sodium sulfateand concentrated. The residue was purified by preparative HPLC (column:Chromatorex C18; 200*40 mm, 10 μM, flow 100 mL/min, gradientacetonitrile/water (containing 0.1% trifluoroacetic acid) 10/90 to 95/5)was added to yield the desired compound

LC-MS (method 11): R_(t)=1.42 min; MS (ESIpos): m/z=464 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.149 (0.25), −0.008(2.29), 0.008 (2.00), 0.146 (0.27), 0.875 (8.29), 0.888 (10.54), 0.891(10.59), 0.904 (9.12), 1.235 (0.54), 1.364 (0.54), 1.381 (1.06), 1.397(1.28), 1.413 (1.26), 1.430 (0.74), 1.540 (0.56), 1.557 (1.00), 1.573(1.22), 1.590 (1.00), 1.606 (0.54), 1.623 (0.25), 1.644 (0.86), 1.664(1.04), 1.678 (0.96), 1.697 (0.79), 1.713 (0.54), 1.816 (0.40), 1.849(15.01), 1.967 (0.33), 1.985 (0.35), 2.073 (0.33), 2.142 (0.28), 2.233(15.48), 2.262 (0.46), 2.328 (0.47), 2.366 (0.49), 2.389 (0.24), 2.614(16.00), 2.670 (0.44), 2.710 (0.44), 3.472 (4.07), 4.610 (1.18), 4.630(1.61), 4.646 (1.13), 7.356 (3.73), 7.379 (5.20), 7.401 (3.13), 7.508(3.01), 7.514 (1.44), 7.522 (3.37), 7.530 (2.69), 7.544 (2.18), 8.441(4.03), 9.371 (3.08).

Example 457N-(4-chloro-1-methyl-3-phenyl-1H-pyrazol-5-yl)-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged with4-chloro-1-methyl-3-phenyl-1H-pyrazol-5-amine (109 mg, 527 μmol) andsodium phenolate (83.5 mg, 719 μmol) and the contents were suspended in1,4-dioxane (1.2 mL). The reaction mixture was degassed with Ar for 3min. 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (100 mg, 479μmol), tris(dibenzylideneacetone)dipalladium (5.71 mg, 6.23 μmol) andXantPhos (8.32 mg, 14.4 μmol) were added and the reaction mixture wasdegassed again for 1 min. The vial was sealed and heated at 80° C.overnight while vigorously shaking. After cooling to ambienttemperature, the reaction mixture was filtered, diluted withdimethylsulfoxide and purified by preparative HPLC (method 4) to yieldthe desired product (15 mg, 8% yield).

LC-MS (method 10): R_(t)=2.14 min; MS (ESIpos): m/z=380 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (1.38), 0.008(1.29), 1.646 (0.50), 2.189 (10.90), 2.328 (0.17), 2.524 (0.66), 2.638(15.99), 2.665 (0.23), 2.670 (0.24), 2.710 (0.16), 3.734 (16.00), 6.162(3.96), 7.101 (0.20), 7.169 (0.16), 7.368 (0.42), 7.384 (1.09), 7.402(2.45), 7.421 (1.75), 7.466 (3.19), 7.486 (4.98), 7.504 (2.18), 7.857(4.04), 7.875 (3.86), 7.878 (2.88), 8.502 (2.69), 9.680 (4.25).

Example 4582-[1-(6-{[1-(cyclopropylmethyl)-3-(5-fluoropyridin-2-yl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]propan-2-ol

A solution of ethyl1-(6-{[1-(cyclopropylmethyl)-3-(5-fluoropyridin-2-yl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(52.0 mg, 106 μmol) in tetrahydrofuran (2.0 ml, 25 mmol) was treated at0° C. with chloro(methyl)magnesium (120 μl, 3.0 M, 370 μmol) and stirredovernight at ambient temperature. No full conversion was observed.Therefore additional chloro(methyl)magnesium (120 μl, 3.0 M, 370 μmol)was added at 0° C. and the mixture was stirred three hours at ambienttemperature. The mixture was diluted with potassium sodium tartratesolution and water and extracted with ethyl acetate. The combinedorganic phases were dried over Extrelut NT3 and concentrated underreduced pressure. The crude product was purified using preparative HPLC(method: column: Reprosil C18; 10 ∞m; 125×30 mm/flow: 50 mL/min/solvent:A=water (0.01% formic acid), B=acetonitrile/grradient: 0.00-5.00 min=10%B, 6.50 min=20% B, 17.0-19.75 min=100% B, 19.75-23.00 min=90% B) toyield 30.2 mg (60%) of the desired product.

LC-MS (method 9): R_(t)=1.00 min; MS (ESIpos): m/z=477 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.006 (1.44), 0.007(0.80), 0.307 (2.23), 0.317 (2.31), 0.436 (2.29), 0.452 (2.35), 1.023(0.45), 1.036 (0.45), 1.195 (0.68), 1.200 (0.64), 1.209 (0.99), 1.219(0.58), 1.224 (0.60), 1.461 (13.86), 1.491 (0.54), 1.969 (0.43), 2.146(16.00), 2.264 (1.88), 2.725 (0.70), 2.740 (14.95), 3.856 (1.79), 3.869(1.77), 4.839 (0.47), 4.852 (3.15), 7.751 (0.66), 7.757 (0.74), 7.769(1.40), 7.775 (1.48), 7.786 (0.78), 7.792 (0.82), 7.985 (0.95), 7.994(1.01), 8.003 (0.93), 8.012 (0.82), 8.463 (0.54), 8.590 (2.76), 8.595(2.76), 9.381 (0.62).

Example 459(±)-4-{3-[(6-{4-[cyclopropyl(hydroxy)methyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-yl)amino]-4-methoxy-1-methyl-1H-pyrazol-5-yl}benzonitrile(racemic)

Under an argon atmosphere a solution of4-(3-{[6-(4-formyl-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-4-methoxy-1-methyl-1H-pyrazol-5-yl)benzonitrile(19.0 mg, 44.3 μmol) in tetrahydrofuran (1.0 ml, 12 mmol) was treatedwith bromo(cyclopropyl)magnesium (440 μl, 0.50 M in tetrahydrofuran, 220μmol) at 0° C. The resulting mixture was stirred one hour at ambienttemperature. The mixture was purified by preparative HPLC (method:column: Reprosil C18; 10 μm; 125×30 mm/flow: 50 mL/min/solvent: A=water(0.01% formic acid), B=acetonitrile/grradient: 0.00-5.00 min=10% B, 6.50min=20% B, 17.0-19.75 min=100% B, 19.75-23.00 min=90% B) to yield 9.8 mg(47%) of the desired product.

LC-MS (method 9): R_(t)=0.89 min; MS (ESIpos): m/z=471 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.128 (0.60), 0.139(0.68), 0.146 (0.49), 0.338 (0.44), 0.347 (0.61), 0.354 (0.89), 0.364(0.78), 0.369 (1.06), 0.374 (0.74), 0.384 (0.57), 0.499 (0.57), 0.504(0.52), 0.507 (0.45), 0.515 (0.44), 1.191 (0.63), 1.197 (0.41), 1.201(0.41), 1.207 (0.62), 2.247 (0.95), 2.258 (9.62), 2.617 (10.75), 2.627(0.73), 2.662 (0.41), 3.564 (16.00), 3.784 (12.22), 3.953 (0.88), 3.960(0.88), 3.969 (0.86), 3.975 (0.82), 4.947 (2.16), 4.953 (2.12), 5.753(1.93), 7.185 (3.07), 7.186 (3.02), 7.773 (3.25), 7.777 (1.22), 7.787(1.36), 7.790 (3.67), 8.004 (3.82), 8.007 (1.30), 8.017 (1.25), 8.021(3.24), 8.449 (2.33), 8.450 (2.30), 9.411 (1.19).

Example 460(±)-cyclopropyl{1-[6-({1-(cyclopropylmethyl)-3-[4-(difluoromethyl)phenyl]-4-methyl-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3,5-dimethyl-1H-pyrazol-4-yl}methanol(racemate)

A solution of1-[6-({1-(cyclopropylmethyl)-3-[4-(difluoromethyl)phenyl]-4-methyl-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3,5-dimethyl-1H-pyrazole-4-carbaldehyde(165 mg, 346 μmol) on tetrahydrofuran (7.8 ml, 96 mmol) was treated at0° C. with bromo(cyclopropyl)magnesium (3.5 ml, 0.50 M intetrahydrofuran, 1.7 mmol). The mixture was stirred one hour at ambienttemperature. The mixture was diluted with saturated potassium sodiumtartrate solution and water and extracted with ethyl acetate (2×). Thecombined organic phases were dried over Extrelut NT3 and concentratedunder reduced pressure. The crude product was purified by preparativeHPLC (method: column: Reprosil C18; 10 μm; 125×30 mm/flow: 50mL/min/solvent: A=water (0.01% formic acid), B=acetonitrile/grradient:0.00-5.00 min=10% B, 6.50 min=20% B, 17.0-19.75 min=100% B, 19.75-23.00min=90% B) to yield 139 mg (78%) of the desired product.

LC-MS (method 9): R_(t)=1.10 min; MS (ESIpos): m/z=520 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.118 (0.50), 0.127(0.70), 0.137 (0.78), 0.145 (0.58), 0.308 (2.08), 0.317 (2.28), 0.327(0.98), 0.335 (0.76), 0.345 (0.78), 0.353 (0.96), 0.368 (1.15), 0.375(0.95), 0.384 (0.79), 0.393 (0.55), 0.436 (2.15), 0.452 (2.18), 0.489(0.48), 0.499 (0.75), 0.505 (0.71), 0.515 (0.61), 1.035 (0.54), 1.048(0.55), 1.190 (0.93), 1.199 (1.11), 1.205 (1.16), 1.215 (1.28), 1.224(0.68), 1.230 (0.66), 2.053 (13.14), 2.257 (1.65), 2.633 (16.00), 3.860(1.66), 3.873 (1.61), 3.965 (0.76), 3.976 (0.75), 4.969 (1.35), 4.974(1.34), 5.754 (2.74), 6.966 (1.27), 7.078 (2.78), 7.190 (1.14), 7.641(2.59), 7.657 (3.05), 7.851 (2.18), 7.867 (1.91), 8.466 (0.48), 9.382(0.48).

Example 461N-[5-(5-fluoropyridin-2-yl)-1,4-dimethyl-1H-pyrazol-3-yl]-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yflpyrimidine (75.0 mg,314 μmol) and 5-(5-fluoropyridin-2-yl)-1,4-dimethyl-1H-pyrazol-3-amine(71.3 mg, 346 μmol) and the contents were suspended in 1,4-dioxane (1.2ml, 14 mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (8.63 mg, 9.43 μmol) and Xantphos(10.9 mg, 18.9 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (40.1 mg, 346 μmol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. The mixture was leftovernight, the reaction mixture was diluted with water and extractedwith dichloromethane (2×). The remaining residue was suspended in amixture of tetrahydrofuran/water/dimethylsulfoxide, the occurringprecipitate was collected by filtration, washed with tetrahydrofuran anddried to yield 72.1 mg (52%) of the desired product.

LC-MS (method 10): R_(t)=1.79 min; MS (ESIpos): m/z=409 [M+H]⁺

¹H-NMR (500 MHz, CHLOROFORM-d) δ [ppm]: −0.007 (0.55), 2.224 (6.27),2.309 (11.70), 3.782 (16.00), 3.977 (11.28), 7.444 (0.70), 7.453 (0.72),7.462 (0.95), 7.470 (0.96), 7.554 (0.64), 7.559 (0.67), 7.570 (0.82),7.575 (0.84), 7.587 (0.49), 7.593 (0.49), 8.414 (1.30), 8.425 (2.30),8.626 (1.65), 8.631 (1.63).

Example 4624-(4-methoxy-5-{[6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-1-methyl-1H-pyrazol-3-yl)benzonitrile

A microwave vial was charged with4-chloro-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (100 mg,100% purity, 419 μmol) and4-(5-amino-4-methoxy-1-methyl-1H-pyrazol-3-yl)benzonitrile (105 mg, 100%purity, 461 μmol), and the contents were suspended in 1,4-dioxane (1.5mL). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (11.5 mg, 12.6 μmol) and XantPhos(14.5 mg, 25.1 μmol) were added and the reaction mixture was degassedagain for 1 min. Finally, sodium phenolate (53.5 mg, 461 μmol) was addedand the vial was sealed and heated at 85° C. overnight while vigorouslyshaking. After cooling to ambient temperature, the reaction mixture wasdiluted with dimethylsulfoxide, filtered and purified by preparativeHPLC (method 3) to yield the desired product (55 mg, 30% yield).

LC-MS (method 10): R_(t)=1.96 min; MS (ESIpos): m/z=431 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.343 (0.19), 1.530(0.30), 1.647 (0.52), 2.188 (2.14), 2.213 (0.46), 3.650 (5.99), 3.703(9.16), 3.714 (0.78), 3.725 (16.00), 7.372 (0.34), 7.385 (0.35), 7.395(0.38), 7.871 (2.63), 7.875 (0.97), 7.885 (1.16), 7.889 (3.12), 8.034(2.80), 8.038 (0.98), 8.051 (2.15), 8.481 (0.86), 9.501 (0.76).

Example 463N-[1-(4-fluorophenyl)-3,5-dimethyl-1H-pyrazol-4-yl]-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged with4-chloro-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (90.0 mg,100% purity, 377 μmol) and1-(4-fluorophenyl)-3,5-dimethyl-1H-pyrazol-4-amine (100 mg, 85% purity,415 μmol) and the contents were suspended in 1,4-dioxane (1.4 mL). Thereaction mixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (10.4 mg, 11.3 μmol) and XantPhos(13.1 mg, 22.6 μmol) were added and the reaction mixture was degassedagain for 1 min. Finally, sodium phenolate (48.2 mg, 415 μmol) was addedand the vial was sealed and heated at 85° C. overnight while vigorouslyshaking. After cooling to ambient temperature, the reaction mixture wasdiluted with dimethylsulfoxide, filtered and purified by preparativeHPLC (method 3) to yield the desired product (13.5 mg, 9% yield).

LC-MS (method 10): R_(t)=1.91 min; MS (ESIpos): m/z=408 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.544 (0.57), 2.072(16.00), 2.159 (1.40), 2.174 (8.65), 2.520 (0.32), 3.692 (4.70), 7.339(1.20), 7.357 (2.44), 7.374 (1.45), 7.591 (1.03), 8.381 (0.35), 8.844(1.80).

Example 4644-[1-(cyclopropylmethyl)-5-{[6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-4-methyl-1H-pyrazol-3-yl]benzonitrile

A microwave vial was charged with4-chloro-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (100 mg,419 μmol) and4-[5-amino-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(116 mg, 461 μmol), and the contents were suspended in 1,4-dioxane (1.3mL). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (11.5 mg, 12.6 μmol) and XantPhos(14.5 mg, 25.1 μmol) were added and the reaction mixture was degassedagain for 1 min. Finally, sodium phenolate (53.5 mg, 461 μmol) was addedand the vial was sealed and heated at 85° C. overnight while vigorouslyshaking. After cooling to ambient temperature, the reaction mixture wasdiluted with dimethylsulfoxide, filtered and purified by preparativeHPLC (method 4) and further by column chromatography (SNAP Ultra 10 g,cyclohexane/ethyl acetate gradient 90/10 to 30/70) to yield the desiredproduct after lyophilisation (85 mg, 44% yield).

LC-MS (method 11): R_(t)=1.45 min; MS (ESIpos): m/z=455 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (0.81), 0.006(0.48), 0.305 (2.08), 0.315 (2.15), 0.433 (2.21), 0.449 (2.25), 1.162(0.40), 1.176 (0.96), 1.181 (0.36), 1.191 (0.97), 1.197 (0.62), 1.207(0.95), 1.216 (0.57), 1.221 (0.57), 1.231 (0.32), 1.236 (0.22), 1.397(6.06), 1.990 (1.35), 2.061 (16.00), 2.075 (0.89), 2.181 (1.89), 3.699(8.28), 3.861 (1.79), 3.875 (1.71), 4.024 (0.32), 4.038 (0.31), 7.888(1.33), 7.892 (1.01), 7.905 (7.63), 7.912 (4.86), 7.929 (0.95), 8.443(0.48), 9.411 (0.47).

Example 4656-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]-N-[3-(5-fluoropyridin-2-yl)-1,4-dimethyl-1H-pyrazol-5-yl]pyrimidin-4-amine

A microwave vial was charged4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (108mg, 441 μmol) and3-(5-fluoropyridin-2-yl)-1,4-dimethyl-1H-pyrazol-5-amine (100 mg, 485μmol) and the contents were suspended in 1,4-dioxane (1.7 ml, 20 mmol).The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (12.1 mg, 13.2 μmol) and Xantphos(15.3 mg, 26.4 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (56.3 mg, 485 μmol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. The mixture was leftovernight at ambient temperature. The reaction mixture was diluted withwater and extracted with dichloromethane (2×). The combined organicphases were dried over sodium sulfate and concentrated under reducedpressure. The crude product was purified by preparative HPLC (method 3)and further falsh-chromatography (column: SNAP KP-Sil 10 g, solvent: 88%dichloromethane/12% ethyl acetate to 100% ethyl acetate) to yield thedesired product (51.1 mg, 28%).

LC-MS (method 10): R_(t)=2.03 min; MS (ESIpos): m/z=415 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.162 (0.44), 1.176(0.90), 1.191 (0.46), 1.990 (1.64), 2.166 (16.00), 2.281 (1.04), 3.701(3.94), 6.784 (1.57), 7.710 (1.06), 7.753 (0.41), 7.759 (0.45), 7.771(0.85), 7.777 (0.87), 7.789 (0.50), 7.794 (0.49), 7.819 (2.12), 7.927(0.95), 7.978 (0.55), 7.986 (0.62), 7.994 (0.56), 8.003 (0.47), 8.590(1.74), 8.596 (1.68), 9.617 (0.60).

Example 466N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-(3,5-dimethyl-4-nitro-1H-pyrazol-1-yl)pyrimidin-4-amine

Under an argon atmosphere,4-chloro-6-(3,5-dimethyl-4-nitro-1H-pyrazol-1-yl)pyrimidine (500 mg,100% purity, 1.97 mmol) and1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine(532 mg, 2.17 mmol) were suspended in 1,4-dioxane (6.3 mL). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (54.2 mg, 59.1 μmol) and XantPhos(68.4 mg, 118 μmol) were added and the reaction mixture was degassedagain for 1 min. Finally, sodium phenolate (252 mg, 2.17 mmol) was addedand the reaction mixture was heated at 85° C. overnight while vigorouslystirring. After cooling to ambient temperature, the reaction mixture wasdiluted with ethyl acetate and washed with brine. The organic phaseextract was dried over sodium sulfate and concentrated. The residue waspurified by flash column chromatography (SNAP Ultra 25 g,cyclohexane/ethyl acetate 90/10 to 0/100) to yield the desired product(62 mg, 7% yield) and a slightly impure product fraction (281 mg, 95%purity, 29% yield).

LC-MS (method 11): R_(t)=1.51 min; MS (ESIpos): m/z=463 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (0.82), 0.006(0.48), 0.296 (2.21), 0.305 (2.24), 0.430 (2.48), 0.446 (2.55), 1.161(0.54), 1.175 (1.15), 1.181 (0.75), 1.189 (1.02), 1.196 (1.05), 1.211(0.68), 1.221 (0.37), 1.237 (0.24), 1.398 (10.29), 1.988 (1.73), 2.011(16.00), 2.119 (0.34), 2.368 (0.51), 2.636 (0.27), 2.993 (5.30), 3.029(0.27), 3.089 (0.27), 3.568 (5.03), 3.838 (1.60), 4.023 (0.37), 4.037(0.37), 7.257 (2.31), 7.274 (4.69), 7.292 (2.62), 7.727 (1.83), 8.574(0.27), 9.619 (0.20).

Example 4676-(3,5-dimethyl-1H-pyrazol-1-yl)-N-[3-(5-fluoropyridin-2-yl)-1,4-dimethyl-1H-pyrazol-5-yl]pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (92.0 mg, 441 μmol)and 3-(5-fluoropyridin-2-yl)-1,4-dimethyl-1H-pyrazol-5-amine (100 mg,485 μmol) and the contents were suspended in 1,4-dioxane (1.7 ml, 20mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (12.1 mg, 13.2 μmol) and Xantphos(15.3 mg, 26.4 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (56.3 mg, 485 p.mol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. The mixture was leftovernight at ambient temperature. The reaction mixture was diluted withwater and extracted with dichloromethane (2×). The combined organicphases were dried over sodium sulfate and concentrated under reducedpressure. The crude product was purified by preparative HPLC (method 7)and further flash-chromatography to yield the desired product (35.4 mg,21%).

LC-MS (method 10): R_(t)=1.91 min; MS (ESIpos): m/z=379 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.078 (0.76), 1.092(1.53), 1.106 (0.76), 2.163 (16.00), 2.228 (0.75), 2.630 (11.81), 2.662(0.53), 3.377 (0.77), 3.391 (0.76), 3.694 (7.29), 6.141 (2.18), 7.749(0.52), 7.755 (0.57), 7.767 (1.11), 7.773 (1.16), 7.785 (0.63), 7.791(0.63), 7.974 (0.82), 7.983 (0.87), 7.992 (0.76), 8.001 (0.69), 8.471(0.55), 8.587 (2.14), 8.592 (2.11), 9.427 (1.90).

Example 468N-[3-(5-fluoropyridin-2-yl)-1,4-dimethyl-1H-pyrazol-5-yl]-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (75.0 mg,314 μmol) and 3-(5-fluoropyridin-2-yl)-1,4-dimethyl-1H-pyrazol-5-amine(71.3 mg, 346 μmol) and the contents were suspended in 1,4-dioxane (1.2ml, 14 mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (8.63 mg, 9.43 μmol) and Xantphos(10.9 mg, 18.9 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (40.1 mg, 346 μmol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. The mixture was leftovernight. The reaction mixture was diluted with water and extractedwith dichloromethane (2×). The combined organic phases were dried oversodium sulfate and concentrated under reduced pressure. The crudeproduct was purified by preparative HPLC (method 7) and furtherflash-chromatography (column: SNAP KP-Sil 10 g, solvent: 88%dichloromethane/12% ethyl acetate to 100% ethyl acetate) to yield thedesired product (18.7 mg, 15%).

LC-MS (method 10): R_(t)=1.91 min; MS (ESIpos): m/z=409 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.079 (1.92), 1.093(3.88), 1.107 (1.92), 2.161 (16.00), 2.177 (2.10), 3.363 (0.67), 3.377(1.91), 3.391 (1.88), 3.405 (0.62), 3.692 (8.83), 3.699 (9.77), 7.749(0.55), 7.755 (0.61), 7.766 (1.18), 7.772 (1.25), 7.784 (0.69), 7.790(0.70), 7.975 (0.84), 7.984 (0.91), 7.992 (0.81), 8.001 (0.73), 8.456(0.57), 8.586 (2.25), 8.592 (2.25), 9.415 (1.91).

Example 469N-[4-(difluoromethoxy)-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidin-4-amine

A microwave vial was charged with4-(difluoromethoxy)-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (120mg, 467 μmol),4-chloro-6-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidine(142 mg, 513 μmol) and sodium phenolate (59.6 mg, 513 μmol) and thecontents were suspended in 1,4-dioxane (1.5 mL). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium(12.8 mg, 14.0 μmol) and XantPhos (16.2 mg, 28.0 μmol) were added andthe reaction mixture was degassed again for 1 min. The vial was sealedand heated at 85° C. overnight while vigorously shaking. After coolingto ambient temperature, the suspension was diluted with ethyl acetateand filter over celite. The filtrate was concentrated, the residue wasredissolved in dimethylsulfoxide and purified by preparative HPLC(method 4) to yield the desired product (84 mg, 36% yield).

LC-MS (method 11): Rt=1.55 min; MS (ESIpos): m/z=498 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (1.49), 0.007(1.00), 2.321 (6.57), 2.324 (6.32), 2.748 (6.75), 2.751 (6.47), 3.729(16.00), 6.651 (1.28), 6.798 (2.49), 6.945 (1.06), 7.378 (1.06), 7.387(2.33), 7.391 (0.84), 7.400 (0.96), 7.404 (4.39), 7.409 (0.84), 7.418(0.78), 7.422 (2.37), 7.589 (2.33), 7.593 (0.96), 7.599 (2.52), 7.606(2.18), 7.613 (0.84), 7.617 (1.93), 8.551 (2.65), 9.746 (1.21).

Example 470N-[4-(difluoromethoxy)-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged with4-(difluoromethoxy)-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (100mg, 389 μmol),4-chloro-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (102 mg,428 μmol) and sodium phenolate (49.6 mg, 428 μmol) and the contents weresuspended in 1,4-dioxane (1.5 mL). The reaction mixture was degassedwith Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (10.7 mg, 11.7μmol) and XantPhos (13.5 mg, 23.3 μmol) were added and the reactionmixture was degassed again for 1 min. The vial was sealed and heated at85° C. overnight while vigorously shaking. After cooling to ambienttemperature, the suspension was diluted with ethyl acetate and filterover celite. The filtrate was concentrated, the residue was redissolvedin dimethylsulfoxide and purified by preparative HPLC (method 3) toyield the desired product (75 mg, 40% yield).

LC-MS (method 11): R_(t)=1.39 min; MS (ESIpos): m/z=460 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (1.06), 0.006(0.63), 2.205 (10.36), 3.707 (16.00), 3.727 (10.73), 6.643 (0.88), 6.790(1.71), 6.938 (0.73), 7.310 (1.39), 7.385 (1.41), 7.389 (0.53), 7.403(2.95), 7.407 (0.63), 7.416 (0.55), 7.421 (1.59), 7.587 (1.61), 7.591(0.71), 7.597 (1.76), 7.604 (1.49), 7.611 (0.63), 7.615 (1.31), 8.440(2.32), 8.442 (2.22), 9.470 (1.94).

Example 4711-(6-{[4-(difluoromethoxy)-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbonitrile

A microwave vial was charged with4-(difluoromethoxy)-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-amine (100mg, 389 μmol),1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbonitrile (99.9mg, 428 μmol) and sodium phenolate (49.6 mg, 428 μmol) and the contentswere suspended in 1,4-dioxane (1.5 mL). The reaction mixture wasdegassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (10.7mg, 11.7 μmol) and XantPhos (13.5 mg, 23.3 μmol) were added and thereaction mixture was degassed again for 1 min. The vial was sealed andheated at 85° C. overnight while vigorously shaking. After cooling toambient temperature, the suspension was diluted with ethyl acetate andfilter over celite. The filtrate was concentrated, the residue wasredissolved in dimethylsulfoxide and purified by preparative HPLC(method 3) to yield the desired product (36 mg, 20% yield).

LC-MS (method 11): R_(t)=1.39 min; MS (ESIpos): m/z=455 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (1.40), 0.007(0.93), 2.349 (14.87), 2.793 (16.00), 3.730 (14.77), 6.646 (1.20), 6.794(2.33), 6.941 (1.00), 7.387 (2.26), 7.391 (1.23), 7.400 (1.53), 7.404(4.46), 7.409 (0.96), 7.418 (0.80), 7.422 (2.30), 7.587 (2.20), 7.592(0.93), 7.598 (2.40), 7.605 (2.10), 7.612 (0.83), 7.616 (1.83), 8.549(2.43), 9.766 (1.06).

Example 4724-(1,4-dimethyl-5-{[6-(3-oxo-1,3,4,5,6,7-hexahydro-2H-indazol-2-yl)pyrimidin-4-yl]amino}-1H-pyrazol-3-yl)benzonitrile

A solution of4-{5-[(6-hydrazinylpyrimidin-4-yl)amino]-1,4-dimethyl-1H-pyrazol-3-yl}benzonitrile(90.0 mg, 281 μmol) in methanol (3.0 ml, 74 mmol) was treated withmethyl 2-oxocyclohexanecarboxylate (41 μl, 280 μmol) and stirred for 4hours at 80° C. The mixture was concentrated under reduced pressure andpurified by preparative HPLC (method 7) to yield 33.0 mg (28%) of thedesired product.

LC-MS (method 10): R_(t)=1.68 min; MS (ESIpos): m/z=427 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (0.98), 0.007(0.81), 1.635 (1.21), 1.645 (1.30), 1.694 (1.30), 1.704 (1.25), 2.059(12.99), 2.073 (0.66), 2.078 (0.65), 2.130 (1.44), 2.455 (1.17), 2.466(2.10), 2.477 (1.22), 3.666 (0.43), 3.687 (8.59), 7.870 (0.78), 7.888(16.00), 7.900 (1.16), 8.433 (0.91), 9.495 (2.25), 11.428 (1.72).

Example 473N-{3-[6-(difluoromethyl)pyridin-3-yl]-1,4-dimethyl-1H-pyrazol-5-yl}-6-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidin-4-amine

A microwave vial was charged with3-[6-(difluoromethyl)pyridin-3-yl]-1,4-dimethyl-1H-pyrazol-5-amine (80.0mg, 336 μmol) and4-chloro-6-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidine(102 mg, 369 μmol) and the contents were suspended in 1,4-dioxane (1.2mL). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (9.22 mg, 10.1 μmol), XantPhos(11.7 mg, 20.1 μmol) and sodium phenolate (42.9 mg, 369 μmol) were addedand the reaction mixture was degassed again for 1 min. The vial wassealed and heated at 85° C. overnight while vigorously shaking. Aftercooling to ambient temperature, the reaction mixture was diluted withethyl acetate, filtered and concentrated. The residue was redissolved indimethylsulfoxide and purified by preparative HPLC (method 4) to yieldthe desired product (64 mg, 37% yield).

LC-MS (method 11): R_(t)=1.47 min; MS (ESIpos): m/z=479 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.567 (0.33), 1.915(0.61), 2.088 (16.00), 2.315 (2.25), 2.744 (0.62), 2.747 (0.66), 2.762(6.37), 3.718 (6.95), 3.758 (1.12), 6.894 (1.28), 7.004 (2.83), 7.064(0.20), 7.115 (1.11), 7.346 (0.59), 7.378 (0.67), 7.457 (0.22), 7.463(0.84), 7.466 (0.82), 7.471 (0.34), 7.478 (0.51), 7.767 (1.91), 7.783(2.18), 7.793 (0.47), 7.796 (0.49), 7.807 (0.37), 7.812 (0.42), 7.818(0.44), 8.255 (0.98), 8.259 (0.98), 8.272 (0.92), 8.275 (0.91), 8.551(0.41), 8.563 (0.46), 9.003 (1.81), 9.687 (0.58).

Example 4746-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-{3-[6-(difluoromethyl)pyridin-3-yl]-1,4-dimethyl-1H-pyrazol-5-yl}pyrimidin-4-amine

A microwave vial was charged with3-[6-(difluoromethyl)pyridin-3-yl]-1,4-dimethyl-1H-pyrazol-5-amine (80.0mg, 336 μmol),4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (89.8 mg,369 μmol) and the contents were suspended in 1,4-dioxane (1.2 mL). Thereaction mixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (9.22 mg, 10.1 μmol), XantPhos(11.7 mg, 20.1 μmol) and sodium phenolate (42.9 mg, 369 μmol) were addedand the reaction mixture was degassed again for 1 min. The vial wassealed and heated at 85° C. overnight while vigorously shaking. Aftercooling to ambient temperature, the reaction mixture was diluted withethyl acetate, filtered through Celite and concentrated. The residue wasredissolved in dimethylsulfoxide and purified by preparative HPLC(method 4) to yield the desired product (18.6 mg, 12% yield).

LC-MS (method 11): R_(t)=1.44 min; MS (ESIpos): m/z=445 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (0.49), 0.007(0.30), 2.081 (16.00), 2.221 (2.13), 2.363 (0.19), 2.651 (15.28), 3.708(7.33), 3.757 (0.15), 6.893 (1.14), 7.003 (2.51), 7.113 (0.99), 7.345(0.23), 7.377 (0.27), 7.463 (0.30), 7.465 (0.30), 7.477 (0.19), 7.765(1.67), 7.781 (1.82), 7.796 (0.19), 7.811 (0.19), 7.816 (0.19), 8.254(0.84), 8.271 (0.80), 8.512 (0.53), 9.001 (1.56), 9.576 (0.68).

Example 475N-{1-(cyclopropylmethyl)-3-[4-(difluoromethoxy)phenyl]-4-methyl-1H-pyrazol-5-yl}-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-amine

In a sealed microwave tube under argon,1-(cyclopropylmethyl)-3-[4-(difluoromethoxy)phenyl]-4-methyl-1H-pyrazol-5-amine(60.0 mg, 205 μmol),4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (55.0mg, 225 μmol), sodium phenolate (26.1 mg, 225 μmol),tris(dibenzylidenaceton)dipalladium (5.62 mg, 6.14 μmol), Xantphos (6.49mg, 12.3 μmol) were dissolved in 1,4-dioxane (980 μl). The reactionmixture was heated at 90° C. for 45 minutes. The cooled reaction mixturewas diluted with dichloromethane, washed with a saturated aqueoussolution of sodium hydrogen carbonate and the aqueous phase thenextracted twice with dichloromethane. The combined organic phase s weredried with sodium sulfate and concentrated in vacuo. The crude productwas purified by flash-chromatography on silica gel (Gradient 7% to 60%ethylacetate in cyclohexane, column: Biotage SNAP Ultra 25 g) to yield63.5 mg (100% purity, 62% yield) of the desired product.

LC-MS (Method 10): R_(t)=2.33 min; MS (ESIpos): m/z=502 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.300 (2.78), 0.423(3.08), 0.439 (3.10), 1.193 (1.40), 2.017 (16.00), 2.282 (1.58), 2.700(0.55), 3.838 (2.05), 6.781 (2.11), 7.130 (2.76), 7.247 (4.44), 7.264(4.66), 7.278 (5.92), 7.426 (2.64), 7.709 (1.87), 7.744 (1.97), 7.817(3.69), 7.926 (1.52), 8.487 (0.37), 9.521 (0.26).

Example 476N-{1-(cyclopropylmethyl)-3-[4-(difluoromethoxy)phenyl]-4-methyl-1H-pyrazol-5-yl}-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

In a sealed microwave tube under argon,1-(cyclopropylmethyl)-3-[4-(difluoromethoxy)phenyl]-4-methyl-1H-pyrazol-5-amine(60.0 mg, 205 μmol), 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine(46.9 mg, 225 μmol), sodium phenolate (26.1 mg, 225 μmol),tris(dibenzylidenaceton)dipalladium (5.62 mg, 6.14 μmol), Xantphos (6.49mg, 12.3 μmol) were dissolved in 1,4-dioxane (980 μl). The reactionmixture was heated at 90° C. for 45 minutes. The cooled reaction mixturewas diluted with dichloromethane, washed with a saturated aqueoussolution of sodium hydrogen carbonate and the aqueous phase thenextracted twice with dichloromethane. The combined organic phase s weredried with sodium sulfate and concentrated in vacuo. The crude productwas purified by flash-chromatography on silica gel (Gradient 7% to 60%ethylacetate in cyclohexane, column: Biotage SNAP Ultra 25 g) to yield60.0 mg (100% purity, 63% yield) of the desired product.

LC-MS (Method 10): R_(t)=2.29 min; MS (ESIpos): m/z=466 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.296 (2.41), 0.305(2.48), 0.425 (2.54), 0.441 (2.60), 1.183 (0.71), 1.189 (0.71), 1.199(1.11), 1.208 (0.65), 1.214 (0.66), 2.016 (16.00), 2.169 (2.29), 2.630(15.40), 3.833 (2.08), 3.846 (2.02), 6.140 (2.47), 7.130 (2.15), 7.246(4.35), 7.264 (4.54), 7.278 (4.53), 7.427 (2.04), 7.742 (2.52), 7.759(2.35), 8.464 (0.55), 9.370 (0.53).

Example 4771-[6-({1-(cyclopropylmethyl)-3-[4-(difluoromethoxy)phenyl]-4-methyl-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3,5-dimethyl-1H-pyrazole-4-carbonitrile

In a sealed microwave tube under argon,1-(cyclopropylmethyl)-3-[4-(difluoromethoxy)phenyl]-4-methyl-1H-pyrazol-5-amine(60.0 mg, 205 μmol),1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbonitrile (52.6mg, 225 μmol), sodium phenolate (26.1 mg, 225 μmol),tris(dibenzylidenaceton)dipalladium (5.62 mg, 6.14 μmol), Xantphos (6.49mg, 12.3 μmol) were dissolved in 1,4-dioxane (980 μl). The reactionmixture was heated at 90° C. for 45 minutes. The cooled reaction mixturewas diluted with dichloromethane, washed with a saturated aqueoussolution of sodium hydrogen carbonate and the aqueous phase thenextracted twice with dichloromethane. The combined organic phase s weredried with sodium sulfate and concentrated in vacuo. The crude productwas purified by flash-chromatography on silica gel (gradient 7% to 60%ethylacetate in cyclohexane, column: Biotage SNAP Ultra 25 g) and thenby preparative TLC (cyclohexane:ethylacetate 7:3) to yield 38.4 mg (100%purity, 38% yield) of the desired product.

LC-MS (Method 10): R_(t)=2.24 min; MS (ESIpos): m/z=491 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (10.09), 0.006(6.62), 0.298 (2.05), 0.422 (2.31), 0.438 (2.33), 1.188 (1.01), 2.010(15.46), 2.328 (1.18), 2.404 (1.08), 2.795 (16.00), 2.870 (0.99), 3.833(1.56), 7.129 (2.26), 7.244 (3.72), 7.261 (3.86), 7.277 (4.88), 7.425(2.12), 7.735 (1.77), 7.750 (1.67), 8.534 (0.26), 9.549 (0.19).

Example 478

N-{1-(cyclopropylmethyl)-3-[4-(difluoromethoxy)phenyl]-4-methyl-1H-pyrazol-5-yl}-6-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidin-4-amine

In a sealed microwave tube under argon,1-(cyclopropylmethyl)-3-[4-(difluoromethoxy)phenyl]-4-methyl-1H-pyrazol-5-amine(60.0 mg, 205 μmol),4-chloro-6-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidine(62.2 mg, 225 μmol), sodium phenolate (26.1 mg, 225 μmol),tris(dibenzylidenaceton)dipalladium (5.62 mg, 6.14 μmol), Xantphos (6.49mg, 12.3 μmol) were dissolved in 1,4-dioxane (980 μl). The reactionmixture was heated at 90° C. for 45 minutes. The cooled reaction mixturewas diluted with dichloromethane, washed with a saturated aqueoussolution of sodium hydrogen carbonate and the aqueous phase thenextracted twice with dichloromethane. The combined organic phase s weredried with sodium sulfate and concentrated in vacuo. The crude productwas purified by flash-chromatography on silica gel (Gradient 7% to 60%ethylacetate in cyclohexane, column: Biotage SNAP Ultra 25 g) and thenby preparative HPLC (Method 19) to yield 49.3 mg (100% purity, 45%yield) of the desired product.

LC-MS (Method 10): R_(t)=2.52 min; MS (ESIpos): m/z=534 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.296 (2.26), 0.305(2.29), 0.429 (2.51), 0.445 (2.54), 1.172 (0.41), 1.181 (0.73), 1.188(0.73), 1.197 (1.11), 1.207 (0.67), 1.211 (0.69), 2.016 (16.00), 2.303(1.34), 2.760 (7.73), 3.838 (1.72), 3.851 (1.68), 7.130 (2.39), 7.245(4.32), 7.263 (4.55), 7.278 (5.18), 7.426 (2.26), 7.737 (2.28), 7.753(2.17).

Example 4796-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-[5-(5-fluoropyridin-2-yl)-1,4-dimethyl-1H-pyrazol-3-yl]pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (108 mg,444 μmol) and 5-(5-fluoropyridin-2-yl)-1,4-dimethyl-1H-pyrazol-3-amine(101 mg, 488 μmol) and the contents were suspended in 1,4-dioxane (1.7ml, 20 mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (12.2 mg, 13.3 μmol) and Xantphos(15.4 mg, 26.6 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (56.6 mg, 488 μmol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. The mixture was leftat ambient temperature overnight. The reaction mixture was diluted withwater and extracted with dichloromethane (2×). The combined organicphases were dried over sodium sulfate and concentrated under reducedpressure. The crude product was purified by preparative HPLC (method:column: Reprosil C18; 10 μm; 125×30 mm/flow: 50 ml/min/eluent: A=water(0.01% formic acid), B=acetonitrile/grradient: 0.00-5.00 min=10% B, 6.50min=20% B, 17.0-19.75 min=100% B, 19.75-23.00min=90% B) to yield thedesired product (54.7 mg, 30%).

LC-MS (method 10): R_(t)=2.17 min; MS (ESIpos): m/z=413 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.956 (13.71), 2.219(15.24), 2.640 (16.00), 3.571 (0.70), 3.853 (15.82), 7.307 (3.21), 7.709(1.68), 7.717 (2.01), 7.725 (2.25), 7.734 (2.01), 7.905 (1.42), 7.917(2.12), 7.922 (2.21), 7.934 (1.24), 8.482 (4.09), 8.778 (3.70), 9.510(3.78).

Example 480N-{1-(cyclopropylmethyl)-4-methyl-3-[4-(methylamino)phenyl]-1H-pyrazol-5-yl}-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

In a sealed microwave tube under argon,1-(cyclopropylmethyl)-4-methyl-3-[4-(methylamino)phenyl]-1H-pyrazol-5-amine(60.0 mg, 234 μmol), 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine(53.7 mg, 257 μmol), sodium phenolate (29.9 mg, 257 μmol),tris(dibenzylidenaceton)dipalladium (6.43 mg, 7.02 μmol), Xantphos (7.42mg, 14.0 μmol) were dissolved in 1,4-dioxane (1.1 ml). The reactionmixture was heated at 90° C. for 45 minutes. The cooled reaction mixturewas diluted with dichloromethane, washed with a saturated aqueoussolution of sodium hydrogen carbonate and the aqueous phase thenextracted twice with dichloromethane. The combined organic phase s weredried with sodium sulfate and concentrated in vacuo. The crude productwas purified by flash-chromatography on silica gel (Gradient 10% to 80%ethylacetate in cyclohexane, column: Biotage SNAP Ultra 10 g) to yield77.5 mg (100% purity, 77% yield) of the desired product.

LC-MS (Method 10): R_(t)=1.99 min; MS (ESIpos): m/z=429 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.275 (2.31), 0.284(2.34), 0.408 (2.55), 0.424 (2.62), 1.151 (0.42), 1.161 (0.77), 1.167(0.77), 1.176 (1.19), 1.186 (0.73), 1.190 (0.70), 1.963 (15.55), 2.161(2.20), 2.627 (16.00), 2.703 (11.56), 2.713 (11.35), 3.355 (0.45), 3.783(2.06), 3.795 (1.99), 5.725 (1.12), 5.734 (1.08), 6.131 (2.34), 6.590(5.24), 6.607 (5.24), 7.432 (2.41), 7.448 (2.24), 8.456 (0.49), 9.302(0.52).

Example 4816-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]-N-{3-[6-(difluoromethyl)pyridin-3-yl]-1,4-dimethyl-1H-pyrazol-5-yl}pyrimidin-4-amine

A microwave vial was charged with3-[6-(difluoromethyl)pyridin-3-yl]-1,4-dimethyl-1H-pyrazol-5-amine (80.0mg, 336 μmol) and4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (90.4mg, 369 μmol) and the contents were suspended in 1,4-dioxane (1.2 mL).The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (9.22 mg, 10.1 μmol), XantPhos(11.7 mg, 20.1 μmol) and sodium phenolate (42.9 mg, 369 μmol) were addedand the reaction mixture was degassed again for 1 min. The vial wassealed and heated at 85° C. overnight while vigorously shaking. Aftercooling to ambient temperature, the reaction mixture was filtered andconcentrated. The residue was redissolved in dimethylsulfoxide andpurified by preparative HPLC (method 4) to yield the desired product (55mg, 35% yield).

LC-MS (method 11): R_(t)=1.34 min; MS (ESIpos): m/z=447 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (0.44), 1.908(0.92), 2.086 (16.00), 2.300 (2.64), 2.336 (0.78), 3.715 (5.80), 3.768(1.59), 6.776 (0.41), 6.794 (2.03), 6.895 (1.22), 7.005 (2.64), 7.115(1.05), 7.712 (1.02), 7.767 (1.73), 7.784 (1.83), 7.821 (2.07), 7.930(0.92), 8.261 (0.78), 8.278 (0.75), 8.490 (0.41), 8.511 (0.44), 9.007(1.46), 9.656 (0.71).

Example 4826-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-[1-(cyclopropylmethyl)-3-(4-methoxyphenyl)-4-methyl-1H-pyrazol-5-yl]pyrimidin-4-amine

In a sealed microwave tube under argon,1-(cyclopropylmethyl)-3-(4-methoxyphenyl)-4-methyl-1H-pyrazol-5-amine(60.0 mg, 233 μmol),4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (68.0 mg,280 μmol), sodium phenolate (29.8 mg, 256 μmol),tris(dibenzylidenaceton)dipalladium (6.41 mg, 6.99 μmol), Xantphos (7.40mg, 14.0 μmol) were dissolved in 1,4-dioxane (1.1 ml). The reactionmixture was heated at 90° C. for 45 minutes. The cooled reaction mixturewas diluted with dichloromethane, washed with a saturated aqueoussolution of sodium hydrogen carbonate and the aqueous phase thenextracted twice with dichloromethane. The combined organic phase s weredried with sodium sulfate and concentrated in vacuo. The crude productwas purified by flash-chromatography on silica gel (Gradient 7% to 60%ethylacetate in cyclohexane, column: Biotage SNAP Ultra 10 g) to yield61.3 mg (100% purity, 57% yield) of the desired product.

LC-MS (Method 10): R_(t)=2.48 min; MS (ESIpos): m/z=464 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.291 (1.20), 0.415(1.29), 0.431 (1.31), 1.184 (0.58), 1.987 (8.04), 2.202 (0.91), 2.644(10.66), 3.794 (16.00), 3.810 (1.06), 3.823 (1.00), 6.999 (2.41), 7.017(2.50), 7.613 (1.12), 7.629 (1.07), 8.498 (0.19), 9.435 (0.15).

Example 4831-(6-{[1-(cyclopropylmethyl)-3-(4-methoxyphenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbonitrile

In a sealed microwave tube under argon,1-(cyclopropylmethyl)-3-(4-methoxyphenyl)-4-methyl-1H-pyrazol-5-amine(60.0 mg, 233 μmol),1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbonitrile (65.4mg, 280 μmol), sodium phenolate (29.8 mg, 256 μmol),tris(dibenzylidenaceton)dipalladium (6.41 mg, 6.99 μmol), Xantphos (7.40mg, 14.0 μmol) were dissolved in 1,4-dioxane (1.1 ml). The reactionmixture was heated at 90° C. for 60 minutes. The cooled reaction mixturewas diluted with dichloromethane, washed with a saturated aqueoussolution of sodium hydrogen carbonate and the aqueous phase thenextracted twice with dichloromethane. The combined organic phase s weredried with sodium sulfate and concentrated in vacuo. The crude productwas purified by flash-chromatography on silica gel (Gradient 7% to 60%ethylacetate in cyclohexane, column: Biotage SNAP Ultra 10 g) and thenby preparative TLC (cyclohexane:ethylacetate 6:4) to yield 50.0 mg (100%purity, 47% yield) of the desired product.

LC-MS (Method 10): R_(t)=2.14 min; MS (ESIpos): m/z=455 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.288 (0.98), 0.415(1.11), 0.431 (1.12), 1.180 (0.49), 1.986 (7.44), 2.324 (0.52), 2.402(0.38), 2.792 (8.06), 2.868 (0.33), 3.793 (16.00), 3.811 (0.77), 6.501(0.04), 6.999 (2.03), 7.016 (2.09), 7.292 (0.06), 7.611 (0.83), 7.626(0.80), 8.539 (0.11), 9.524 (0.08), 9.630 (0.06).

Example 4846-(4-amino-3,5-dimethyl-1H-pyrazol-1-yl)-N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]pyrimidin-4-aminetrifluoroacetate

tert-butyl[6-(4-amino-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl][1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]carbamate(24.0 mg, 45.1 μmol) was dissolved in dichloromethane (800 μL) andtrifluoroacetic acid (800 μL) was added. The reaction mixture wasstirred at ambient temperature for 15 min. The reaction mixture wasconcentrated and the residue redissolved in dichloromethane andconcentrated (3 cycles). The residue was then redissolved inacetonitrile/water and lyophilized to yield the desired product as theTFA salt (25 mg, 93% yield).

LC-MS (method 11): R_(t)=1.16 min; MS (ESIpos): m/z=433 [M+H]⁺

¹H-NMR (600 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.295 (2.65), 0.424(3.05), 0.437 (3.05), 0.854 (0.18), 1.191 (1.53), 1.235 (0.95), 1.649(0.25), 2.005 (15.34), 2.241 (1.48), 2.388 (0.66), 2.616 (0.84), 2.661(16.00), 2.709 (0.50), 2.868 (0.34), 3.828 (2.63), 7.018 (0.48), 7.103(0.50), 7.188 (0.55), 7.268 (2.40), 7.282 (4.35), 7.297 (2.44), 7.730(2.11), 8.500 (0.34), 9.463 (0.38).

Example 485N-{3-[6-(difluoromethyl)pyridin-3-yl]-1,4-dimethyl-1H-pyrazol-5-yl}-6-(4-fluoro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged with3-[6-(difluoromethyl)pyridin-3-yl]-1,4-dimethyl-1H-pyrazol-5-amine (80.0mg, 336 μmol) and4-chloro-6-(4-fluoro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (83.7 mg,369 μmol), and the contents were suspended in 1,4-dioxane (1.2 mL). Thereaction mixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (9.22 mg, 10.1 μmol), XantPhos(11.7 mg, 20.1 μmol) and sodium phenolate (42.9 mg, 369 μmol) were addedand the reaction mixture was degassed again for 1 min. The vial wassealed and heated at 85° C. overnight while vigorously shaking. Aftercooling to ambient temperature, the reaction mixture was diluted withethyl acetate, filtered over Celite and concentrated. The residue wasredissolved in dimethylsulfoxide and purified by preparative HPLC(method 4) to yield the desired product (33 mg, 23% yield).

LC-MS (method 11): Rt=1.37 min; MS (ESIneg): m/z=427 [M−H]−

¹H NMR (500 MHz, dimethylsulfoxide-d6) δ ppm: 2.05-2.12 (s, 3H),2.15-2.28 (br s, 3H), 2.60 (d, J=1.66 Hz, 3H), 3.66-3.81 (s, 3H), 6.99(t, J=55.1 Hz, 1H), 7.01-7.53 (br s, 1H), 7.70-7.85 (m, 1H), 8.18-8.29(m, 1H), 8.37-8.62 (m, 1H), 9.00 (s, 1H), 9.54 (br s, 1H).

Example 486N-[1-(cyclopropylmethyl)-3-(4-methoxyphenyl)-4-methyl-1H-pyrazol-5-yl]-6-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidin-4-amine

In a sealed microwave tube under argon,1-(cyclopropylmethyl)-3-(4-methoxyphenyl)-4-methyl-1H-pyrazol-5-amine(60.0 mg, 233 μmol),4-chloro-6-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidine(77.4 mg, 280 μmol), sodium phenolate (29.8 mg, 256 μmol),tris(dibenzylidenaceton)dipalladium (6.41 mg, 6.99 μmol), Xantphos (7.40mg, 14.0 μmol) were dissolved in 1,4-dioxane (1.1 ml). The reactionmixture was heated at 90° C. for 45 minutes. The cooled reaction mixturewas diluted with dichloromethane, washed with a saturated aqueoussolution of sodium hydrogen carbonate and the aqueous phase thenextracted twice with dichloromethane. The combined organic phase s weredried with sodium sulfate and concentrated in vacuo. The crude productwas purified by flash-chromatography on silica gel (gradient 7% to 60%ethylacetate in cyclohexane, column: Biotage SNAP Ultra 10 g) to yield73.6 mg (100% purity, 63% yield) of the desired product.

LC-MS (Method 9): R_(t)=1.29 min; MS (ESIpos): m/z=498 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.294 (1.10), 0.420(1.21), 0.436 (1.23), 1.187 (0.55), 1.991 (7.54), 2.296 (0.62), 2.756(3.92), 3.793 (16.00), 3.816 (0.87), 6.471 (0.02), 6.999 (2.40), 7.016(2.50), 7.305 (0.06), 7.610 (1.08), 7.626 (1.02), 8.537 (0.13), 9.517(0.09).

Example 487N-{1-(cyclopropylmethyl)-4-methyl-3-[4-(methylamino)phenyl]-1H-pyrazol-5-yl}-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-amine

In a sealed microwave tube under argon,1-(cyclopropylmethyl)-4-methyl-3-[4-(methylamino)phenyl]-1H-pyrazol-5-amine(60.0 mg, 234 μmol),4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (63.0mg, 257 μmol), sodium phenolate (29.9 mg, 257 μmol),tris(dibenzylidenaceton)dipalladium (6.43 mg, 7.02 μmol), Xantphos (7.42mg, 14.0 μmol) were dissolved in 1,4-dioxane (1.1 ml). The reactionmixture was heated at 90° C. for 45 minutes. The cooled reaction mixturewas diluted with dichloromethane, washed with a saturated aqueoussolution of sodium hydrogen carbonate and the aqueous phase thenextracted twice with dichloromethane. The combined organic phase s weredried with sodium sulfate and concentrated in vacuo. The crude productwas purified by flash-chromatography on silica gel (Gradient 8% to 60%ethylacetate in cyclohexane, column: Biotage SNAP Ultra 10 g) and thenby preparative TLC (dichloromethane:ethylacetate 7:3). The resultantresidue was dissolved in dichloromethane and washed with a saturatedaqueous solution of sodium bicarbonate. The aqueous phase was extractedwith dichloromethane and the combined organic phase s dried with sodiumsulfate and concentrated in vacuo to yield 63.2 mg (97% purity, 56%yield) of the desired product.

LC-MS (Method 10): R_(t)=2.07 min; MS (ESIpos): m/z=465 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.278 (2.61), 0.405(3.07), 0.421 (3.08), 1.171 (1.65), 1.232 (0.47), 1.408 (0.61), 1.421(0.32), 1.965 (15.86), 2.269 (1.43), 2.701 (16.00), 2.711 (15.62), 3.792(2.14), 3.837 (0.62), 5.736 (1.13), 6.464 (0.13), 6.589 (5.54), 6.606(5.50), 6.771 (1.89), 7.288 (0.18), 7.437 (1.99), 7.708 (1.85), 7.817(4.02), 7.925 (1.65), 8.472 (0.30), 9.432 (0.23), 9.544 (0.23).

Example 488

N-{1-(cyclopropylmethyl)-4-methyl-3-[4-(methylamino)phenyl]-1H-pyrazol-5-yl}-6-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidin-4-amine

In a sealed microwave tube under argon,1-(cyclopropylmethyl)-4-methyl-3-[4-(methylamino)phenyl]-1H-pyrazol-5-amine(60.0 mg, 234 μmol),4-chloro-6-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidine(71.2 mg, 257 μmol), sodium phenolate (29.9 mg, 257 μmol),tris(dibenzylidenaceton)dipalladium (6.43 mg, 7.02 μmol), Xantphos (7.42mg, 14.0 μmol) were dissolved in 1,4-dioxane (1.1 ml). The reactionmixture was heated at 90° C. for 45 minutes. The cooled reaction mixturewas diluted with dichloromethane, washed with a saturated aqueoussolution of sodium hydrogen carbonate and the aqueous phase thenextracted twice with dichloromethane. The combined organic phase s weredried with sodium sulfate and concentrated in vacuo. The crude productwas purified by flash-chromatography on silica gel (Gradient 8% to 60%ethylacetate in cyclohexane, column: Biotage SNAP Ultra 10 g) and thenby preparative HPLC (Method 19) to yield 63.0 mg (96% purity, 52% yield)of the desired product.

LC-MS (Method 9): R_(t)=1.18 min; MS (ESIpos): m/z=497 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.273 (2.73), 0.411(3.10), 0.426 (3.03), 1.033 (0.62), 1.174 (1.72), 1.233 (0.96), 1.962(16.00), 2.288 (1.55), 2.699 (12.12), 2.709 (11.76), 2.754 (10.12),3.788 (2.24), 5.732 (1.24), 6.474 (0.13), 6.585 (5.65), 6.602 (5.62),7.279 (0.18), 7.424 (2.72), 7.440 (2.46), 8.531 (0.34), 9.502 (0.27).

Example 489N-[1-(cyclopropylmethyl)-3-(4-methoxyphenyl)-4-methyl-1H-pyrazol-5-yl]-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-amine

In a sealed microwave tube under argon,1-(cyclopropylmethyl)-3-(4-methoxyphenyl)-4-methyl-1H-pyrazol-5-amine(60.0 mg, 233 μmol),4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (68.4mg, 280 μmol), sodium phenolate (29.8 mg, 256 μmol),tris(dibenzylidenaceton)dipalladium (6.41 mg, 6.99 μmol), Xantphos (7.40mg, 14.0 μmol) were dissolved in 1,4-dioxane (1.1 ml). The reactionmixture was heated at 90° C. for 45 minutes. The cooled reaction mixturewas diluted with dichloromethane, washed with a saturated aqueoussolution of sodium hydrogen carbonate and the aqueous phase thenextracted twice with dichloromethane. The combined organic phase s weredried with sodium sulfate and concentrated in vacuo. The crude productwas purified by flash-chromatography on silica gel (Gradient 7% to 60%ethylacetate in cyclohexane, column: Biotage SNAP Ultra 10 g) and thenby preparative HPLC (Method 19) to yield 65.0 mg (97% purity, 58% yield)of the desired product.

LC-MS (Method 10): R_(t)=2.24 min; MS (ESIpos): m/z=466 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.291 (1.08), 0.416(1.22), 0.432 (1.23), 1.169 (0.39), 1.185 (0.57), 1.993 (6.20), 2.281(0.60), 2.699 (0.24), 3.795 (16.00), 3.818 (0.85), 6.777 (0.80), 7.002(1.91), 7.020 (1.96), 7.621 (0.76), 7.708 (0.72), 7.817 (1.50), 7.926(0.63), 8.489 (0.13), 9.492 (0.09).

Example 4901-[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]propan-2-one

A solution ethyl[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]acetate(570 mg, 1.13 mmol) in tetrahydrofuran (12 ml, 140 mmol) was treatedwith chloro(methyl)magnesium (1.3 ml, 3.0 M, 4.0 mmol) at 0° C. andstirred for 2 hours at ambient temperature. The mixture was diluted withpotassium sodium tartrate and water, and extracted with ethyl acetate(3×). The combined organic phases were washed with water, dried oversodium sulfate and concentrated under reduced pressure. The crudeproduct was purified by flash-chromatography on silica gel (column:Biotage SNAP Ultra 25 g, solvent: dichloromethane/methanol 20:1) andsubsequently by preparative HPLC (column: 250×20 mm YMC ChiralartCellulose SC, 5 μM, flow: 15 mL/min, solvent: n-heptane 30%/ethanol 70%)to yield 22.0 mg (4%) of the described product along with1-[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]-2-methylpropan-2-ol.

LC-MS (method 10): R_(t)=2.06 min; MS (ESIpos): m/z=474 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (1.30), 0.007(0.93), 0.294 (2.45), 0.303 (2.54), 0.424 (2.59), 0.440 (2.68), 1.086(0.83), 1.119 (0.77), 1.133 (1.41), 1.147 (0.72), 1.171 (0.43), 1.180(0.74), 1.186 (0.75), 1.195 (1.11), 1.205 (0.69), 1.210 (0.69), 2.008(16.00), 2.068 (2.10), 2.142 (13.82), 2.576 (0.81), 2.650 (0.58), 2.858(0.42), 3.589 (4.74), 3.830 (2.03), 3.843 (1.97), 7.255 (2.48), 7.273(4.88), 7.291 (2.54), 7.719 (1.47), 7.730 (1.96), 7.746 (1.30), 8.460(0.55), 9.358 (0.43).

Example 491N-[1-(cyclopropylmethyl)-3-(4-methoxyphenyl)-4-methyl-1H-pyrazol-5-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

In a sealed microwave tube under argon,1-(cyclopropylmethyl)-3-(4-methoxyphenyl)-4-methyl-1H-pyrazol-5-amine(60.0 mg, 233 μmol), 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine(58.4 mg, 280 μmol), sodium phenolate (29.8 mg, 256 μmol),tris(dibenzylidenaceton)dipalladium (6.41 mg, 6.99 μmol), Xantphos (7.40mg, 14.0 μmol) were dissolved in 1,4-dioxane (1.1 ml). The reactionmixture was heated at 90° C. for 45 minutes. The cooled reaction mixturewas diluted with dichloromethane, washed with a saturated aqueoussolution of sodium hydrogen carbonate and the aqueous phase thenextracted twice with dichloromethane. The combined organic phase s weredried with sodium sulfate and concentrated in vacuo. The crude productwas purified by flash-chromatography on silica gel (Gradient 7% to 60%ethylacetate in cyclohexane, column: Biotage SNAP Ultra 10 g) and thenby preparative HPLC (Method 19) to yield 78.0 mg (100% purity, 78%yield) of the desired product.

LC-MS (Method 10): R_(t)=2.18 min; MS (ESIpos): m/z=430 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.285 (1.11), 0.295(1.13), 0.416 (1.20), 0.432 (1.22), 1.163 (0.19), 1.173 (0.38), 1.179(0.35), 1.188 (0.55), 1.198 (0.31), 1.203 (0.31), 1.213 (0.16), 1.990(8.05), 2.163 (1.03), 2.626 (7.44), 3.647 (0.07), 3.794 (16.00), 3.810(1.00), 3.823 (0.94), 3.936 (0.08), 6.134 (1.12), 7.000 (2.45), 7.017(2.52), 7.615 (1.15), 7.632 (1.07), 8.458 (0.24), 9.336 (0.23).

Example 492 ethyl[1-(6-{[5-(4-cyanophenyl)-4-methoxy-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]acetate

A microwave vial was charged ethyl[1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]acetate (252mg, 856 μmol) and4-(3-amino-4-methoxy-1-methyl-1H-pyrazol-5-yl)benzonitrile (215 mg, 942μmol) and the contents were suspended in 1,4-dioxane (13 ml, 150 mmol).The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (23.5 mg, 25.7 μmol) and Xantphos(29.7 mg, 51.4 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (109 mg, 942 μmol) was added. The vial was sealed and heatedat 85° C. for 120 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was filtered adn preparativeHPLC (method: column: Reprosil C18; 10 μm; 125×40 mm/flow: 75ml/min/eluent: A=water (0.1% formic acid), B=acetonitrile/grradient:0.00-5.50 min=10% B, 17.65-19.48 min=95% B, 19.66 min=10% B) and furtherflash-chromatography (column; SNAP Ultra 25 g, solvent:dichloromethane/ethyl acetate 1:1) to yield the desired product (190 mg,46%).

LC-MS (method 9): R_(t)=0.99 min; MS (ESIpos): m/z=487 [M+H]⁺

¹H-NMR (600 MHz, dimethylsulfoxide-d6) δ [ppm]: 1.175 (4.47), 1.187(9.06), 1.199 (4.30), 1.992 (0.43), 2.140 (10.65), 2.572 (12.28), 3.482(6.07), 3.566 (16.00), 3.791 (13.16), 4.060 (1.23), 4.072 (3.80), 4.084(3.81), 4.095 (1.21), 7.198 (3.47), 7.199 (3.37), 7.780 (3.43), 7.783(1.20), 7.791 (1.30), 7.794 (3.75), 8.011 (3.91), 8.014 (1.23), 8.022(1.23), 8.025 (3.35), 8.463 (2.38), 9.470 (0.82).

Example 4934-(4-methoxy-3-{[6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-1-methyl-1H-pyrazol-5-yl)benzonitrile

A microwave vial was charged4-chloro-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (143 mg,597 μmol) and 4-(3-amino-4-methoxy-1-methyl-1H-pyrazol-5-yl)benzonitrile(150 mg, 657 μmol) and the contents were suspended in 1,4-dioxane (2.2ml, 25 mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (16.4 mg, 17.9 μmol) and Xantphos(20.7 mg, 35.8 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (76.3 mg, 657 μmol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. The mixture was leftovernight at ambient temperature. The reaction mixture was filtered andpurified by preparative HPLC (method: column: Reprosil C18; 10 μm;125×30 mm/flow: 50 ml/min/eluent: A=water (0.01% formic acid),B=acetonitrile/grradient: 0.00-5.00 min=10% B, 6.50 min=20% B,17.0-19.75 min=100% B, 19.75-23.00min=90% B) and furtherflash-chromatography (column: KP-Sil 10 g, solvent:dichloromethane/ethylacetate 1:1 to yield the desired product (47 mg,18%).

LC-MS (method 10): R_(t)=1.83 min; MS (ESIpos): m/z=431 [M+H]⁺

¹H-NMR (600 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.005 (0.73), 2.187(10.69), 3.560 (14.60), 3.699 (16.00), 3.788 (12.42), 7.175 (3.54),7.778 (3.30), 7.792 (3.62), 8.012 (3.73), 8.025 (3.21), 8.439 (2.52),9.443 (0.97).

Example 4946-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]-N-[3-(6-methoxypyridin-3-yl)-1,4-dimethyl-1H-pyrazol-5-yl]pyrimidin-4-amine

In a sealed microwave tube under argon,3-(6-methoxypyridin-3-yl)-1,4-dimethyl-1H-pyrazol-5-amine (50.0 mg, 229μmol),4-chloro-6-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidine(76.1 mg, 275 μmol), sodium phenolate (29.3 mg, 252 μmol),tris(dibenzylidenaceton)dipalladium (6.29 mg, 6.87 μmol), Xantphos (7.27mg, 13.7 μmol) were dissolved in 1,4-dioxane (1.1 ml). The reactionmixture was heated at 90° C. for 60 minutes. The cooled reaction mixturewas diluted with dichloromethane, washed with a saturated aqueoussolution of sodium hydrogen carbonate and the aqueous phase thenextracted twice with dichloromethane. The combined organic phase s weredried with sodium sulfate and concentrated in vacuo. The crude productwas purified by flash-chromatography on silica gel (gradient 12% to 100%ethylacetate in cyclohexane, column: Biotage SNAP Ultra 10 g) and thenby preparative TLC (cyclohexane:ethylacetate 1:1) to yield 30.0 mg (100%purity, 29% yield) of the desired product.

LC-MS (Method 9): R_(t)=1.13 min; MS (ESIpos): m/z=459 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 2.010 (10.85), 2.071(2.91), 2.308 (1.10), 2.756 (3.97), 3.163 (0.42), 3.173 (0.45), 3.664(3.97), 3.891 (16.00), 3.926 (0.14), 6.890 (1.36), 6.907 (1.39), 7.977(0.56), 7.981 (0.61), 7.994 (0.56), 7.999 (0.56), 8.435 (1.03), 8.439(1.03), 8.553 (0.26), 9.626 (0.28).

Example 495Cyclopropyl{1-[6-({1-(cyclopropylmethyl)-3-[4-(difluoromethyl)phenyl]-4-methyl-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3,5-dimethyl-1H-pyrazol-4-yl}methanol

A sample of racemiccyclopropyl{1-[6-({1-(cyclopropylmethyl)-3-[4-(difluoromethyl)phenyl]-4-methyl-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3,5-dimethyl-1H-pyrazol-4-yl}methanol(139.2 mg, 270 μMol) was separated using chiral SFC (column: AD-H 5μ250×20 mm, temperature: 40° C., flow: 80 mL/min, wavelength: 210 nM,solvent: 87% carbon dioxide/13% ethanol) to yield 35.80 mg of the secondeluting enantiomer which was further purified by preparative HPLC(method 6) to yield 25.3 mg of the desired product (18% from racemate).

LC-MS (method 10): R_(t)=2.02 min; MS (ESIpos): m/z=520 [M+H]⁺

Chiral SFC (Daicel AD, isocratic carbon dioxide/ethanol 80/20): Rt=2.82min, 96.8% ee

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (2.26), 0.006(1.45), 0.116 (0.66), 0.123 (0.68), 0.133 (0.75), 0.141 (0.56), 0.304(1.99), 0.314 (2.18), 0.332 (0.71), 0.342 (0.77), 0.350 (1.00), 0.364(1.14), 0.370 (0.95), 0.380 (0.77), 0.389 (0.53), 0.432 (2.06), 0.449(2.09), 0.485 (0.49), 0.496 (0.75), 0.502 (0.70), 0.512 (0.61), 1.077(0.54), 1.091 (1.07), 1.105 (0.53), 1.185 (0.92), 1.194 (1.09), 1.200(1.16), 1.210 (1.24), 1.224 (0.65), 2.047 (13.70), 2.252 (1.62), 2.628(16.00), 3.325 (0.60), 3.377 (0.54), 3.390 (0.53), 3.854 (1.62), 3.868(1.53), 3.960 (0.75), 3.969 (0.73), 4.962 (1.58), 4.968 (1.53), 6.964(1.23), 7.076 (2.67), 7.188 (1.09), 7.637 (2.52), 7.654 (2.89), 7.846(2.11), 7.862 (1.79), 8.458 (0.46), 9.374 (0.44).

Example 496Cyclopropyl{1-[6-({1-(cyclopropylmethyl)-3-[4-(difluoromethyl)phenyl]-4-methyl-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3,5-dimethyl-1H-pyrazol-4-yl}methanol

A sample of racemiccyclopropyl{1-[6-({1-(cyclopropylmethyl)-3-[4-(difluoromethyl)phenyl]-4-methyl-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3,5-dimethyl-1H-pyrazol-4-yl}methanol(139.2 mg, 270 μMol) was separated using chiral SFC (column: AD-H 5μ250×20 mm, temperature: 40° C., flow: 80 mL/min, wavelength: 210 nM,solvent: 87% carbon dioxide/13% ethanol) to yield 35.80 mg of the firsteluting enantiomer which was further purified by preparative HPLC(method 6) to yield 19.2 mg of the desired product (14% from racemate).

LC-MS (method 10): R_(t)=2.02 min; MS (ESIpos): m/z=520 [M+H]⁺

Chiral SFC (Daicel AD, isocratic carbon dioxide/ethanol 80/20): Rt=2.48min, >99.5% ee

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (2.01), 0.006(1.31), 0.116 (0.64), 0.123 (0.65), 0.133 (0.76), 0.141 (0.55), 0.304(1.96), 0.314 (2.17), 0.332 (0.71), 0.342 (0.76), 0.350 (1.01), 0.364(1.16), 0.370 (0.96), 0.380 (0.76), 0.389 (0.52), 0.433 (2.05), 0.449(2.10), 0.485 (0.49), 0.496 (0.72), 0.502 (0.69), 0.513 (0.60), 1.185(0.89), 1.194 (1.07), 1.200 (1.12), 1.210 (1.24), 1.225 (0.64), 2.047(13.30), 2.251 (1.59), 2.629 (16.00), 2.690 (1.11), 3.855 (1.58), 3.868(1.54), 3.960 (0.74), 3.970 (0.72), 4.962 (1.61), 4.968 (1.56), 6.964(1.24), 7.076 (2.70), 7.188 (1.11), 7.637 (2.50), 7.654 (2.90), 7.846(2.08), 7.862 (1.80), 8.459 (0.47), 9.373 (0.44).

Example 4971-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-ylacetate

Under an argon atmosphere,1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine(418 mg, 1.70 mmol),1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl acetate (500 mg,1.87 mmol), tris(dibenzylideneacetone)dipalladium (46.8 mg, 51.1 μmol)and XantPhos (59.2 mg, 102 μmol) and were suspended in 1,4-dioxane (4mL). The reaction mixture was degassed with Ar for 5 min. Sodiumphenolate (218 mg, 1.87 mmol) was added and the reaction mixture wasdegassed again for 1 min. The reaction mixture was heated at 85° C.overnight while vigorously stirring. After cooling to ambienttemperature, the reaction mixture was diluted with ethyl acetate,filtered over Celite and concentrated. The residue was purified bypreparative HPLC (column: Chromatorex C18; 125*30 mm, 10 μM, flow 75mL/min, gradient acetonitrile/water (containing 0.1% trifluoroaceticacid) 10/90 to 95/5) to yield the desired product (118 mg, 14% yield).

LC-MS (method 11): R_(t)=1.47 min; MS (ESIpos): m/z=476 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.120 (0.43), −0.007(4.19), 0.007 (3.01), 0.116 (0.43), 0.300 (1.18), 0.424 (1.29), 0.440(1.40), 1.190 (0.54), 2.008 (7.73), 2.072 (8.59), 2.220 (0.43), 2.321(6.87), 2.358 (1.18), 2.362 (1.18), 2.486 (16.00), 2.635 (1.07), 3.830(0.86), 7.256 (1.18), 7.274 (2.47), 7.291 (1.29), 7.732 (0.97).

Example 4986-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-[1-(cyclopropylmethyl)-3-(6-methoxypyridin-3-yl)-4-methyl-1H-pyrazol-5-yl]pyrimidin-4-amine

In a sealed microwave tube under argon,1-(cyclopropylmethyl)-3-(6-methoxypyridin-3-yl)-4-methyl-1H-pyrazol-5-amine(50.0 mg, 194 μmol),4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (56.5 mg,232 μmol), sodium phenolate (24.7 mg, 213 μmol),tris(dibenzylidenaceton)dipalladium (5.32 mg, 5.81 μmol), Xantphos (6.14mg, 11.6 μmol) were dissolved in 1,4-dioxane (920 μl). The reactionmixture was heated at 90° C. for 45 minutes. The cooled reaction mixturewas diluted with dichloromethane, washed with a saturated aqueoussolution of sodium hydrogen carbonate and the aqueous phase thenextracted twice with dichloromethane. The combined organic phase s weredried with sodium sulfate and concentrated in vacuo. The crude productwas purified by flash-chromatography on silica gel (gradient 7% to 60%ethylacetate in cyclohexane, column: Biotage SNAP Ultra 10 g) to yield61.1 mg (100% purity, 68% yield) of the desired product.

LC-MS (Method 10): R_(t)=2.40 min; MS (ESIpos): m/z=465 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.122 (0.10), −0.009(1.05), 0.114 (0.10), 0.289 (1.11), 0.299 (1.15), 0.421 (1.19), 0.437(1.22), 1.176 (0.34), 1.182 (0.33), 1.191 (0.52), 1.205 (0.32), 1.999(7.55), 2.208 (0.99), 2.645 (10.17), 3.826 (0.94), 3.839 (0.91), 3.895(16.00), 6.898 (1.33), 6.915 (1.37), 8.003 (0.46),

Example 4996-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]-N-[3-(6-methoxypyridin-3-yl)-1,4-dimethyl-1H-pyrazol-5-yl]pyrimidin-4-amine

In a sealed microwave tube under argon,3-(6-methoxypyridin-3-yl)-1,4-dimethyl-1H-pyrazol-5-amine (50.0 mg, 229μmol),4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (67.2mg, 275 μmol), sodium phenolate (29.3 mg, 252 μmol),tris(dibenzylidenaceton)dipalladium (6.29 mg, 6.87 μmol), Xantphos (7.27mg, 13.7 μmol) were dissolved in 1,4-dioxane (1.1 ml). The reactionmixture was heated at 90° C. for 60 minutes. The cooled reaction mixturewas diluted with dichloromethane, washed with a saturated aqueoussolution of sodium hydrogen carbonate and the aqueous phase thenextracted twice with dichloromethane. The combined organic phase s weredried with sodium sulfate and concentrated in vacuo. The crude productwas purified by flash-chromatography on silica gel (gradient 12% to 100%ethylacetate in cyclohexane, column: Biotage SNAP Ultra 10 g) to yield60.5 mg (90% purity, 56% yield) of the desired product.

LC-MS (Method 10): R_(t)=1.94 min; MS (ESIpos): m/z=427 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.51), 2.012(9.87), 2.288 (1.10), 2.700 (0.24), 3.664 (3.61), 3.704 (0.27), 3.894(16.00), 3.928 (0.36), 6.787 (1.36), 6.894 (1.28), 6.911 (1.32), 7.709(0.68), 7.818 (1.38), 7.926 (0.60), 7.988 (0.47), 8.004 (0.46), 8.444(0.89), 8.503 (0.26), 9.594 (0.36).

Example 5002-[1-(6-{[4-(difluoromethoxy)-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]propan-2-ol

Under an argon atmosphere, ethyl1-(6-{[4-(difluoromethoxy)-5-(4-fluorophenyl)-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(119 mg, 237 μmol) was dissolved in tetrahydrofuran and the solutioncooled to 0° C. A solution of chloro(methyl)magnesium (395 μl, 3.0 M,1.2 mmol) was added dropwise over 15 min and the reaction mixture wasstirred for 6 h at ambient temperature. Another aliquot ofchloro(methyl)magnesium (395 μl, 3.0 M, 1.2 mmol) was added and thereaction mixture was allowed to stir overnight. The reaction mixture wascarefully quenched by addition of water and aqueous hydrochloric acidsolution (0.5 mL, 2 N). It was extracted with ethyl acetate (3×) and thecombined organic phase extracts were washed with brine, dried oversodium sulfate and concentrated. The residue was purified by flashcolumn chromatography (SNAP Ultra 10 g, cyclohexane/ethyl acetategradient 100/0 to 0/100) to yield the desired product (19 mg, 16% yield)after lyophilization from acetonitrile/water.

LC-MS (method 11): R_(t)=1.27 min; MS (ESIneg): m/z=486 [M−H]⁻

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (0.47), 1.475(16.00), 2.289 (8.05), 2.726 (8.49), 3.696 (0.63), 3.721 (9.06), 4.852(2.05), 6.647 (0.71), 6.795 (1.36), 6.942 (0.59), 7.286 (1.03), 7.383(1.17), 7.387 (0.42), 7.401 (2.41), 7.405 (0.51), 7.415 (0.47), 7.419(1.31), 7.584 (1.34), 7.588 (0.62), 7.595 (1.49), 7.601 (1.27), 7.608(0.53), 7.612 (1.11), 8.463 (1.90), 8.465 (1.78), 9.494 (0.78).

Example 501N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-[4-(ethylamino)-3,5-dimethyl-1H-pyrazol-1-yl]pyrimidin-4-aminetrifluoroacetate

tert-butyl[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]{6-[4-(ethylamino)-3,5-dimethyl-1H-pyrazol-1-yl]pyrimidin-4-yl}carbamate(24.0 mg, 42.8 μmol) was dissolved in dichloromethane (760 μL) andtrifluoroacetic acid (760 μL) was added. The reaction mixture wasstirred at ambient temperature for 20 min. The reaction mixture wasconcentrated and the residue redissolved in dichloromethane andconcentrated (3 cycles). The residue was then redissolved inacetonitrile/water and lyophilized to yield the desired product as theTFA salt (26 mg, 94% yield).

LC-MS (method 11): R_(t)=1.20 min; MS (ESIpos): m/z=461 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.007 (0.84), 0.006(0.39), 0.297 (2.61), 0.424 (2.83), 0.440 (2.81), 0.852 (0.19), 1.122(0.40), 1.136 (0.79), 1.161 (2.69), 1.175 (5.17), 1.190 (3.20), 1.235(0.82), 1.322 (0.21), 1.649 (0.70), 2.005 (16.00), 2.069 (0.31), 2.280(1.57), 2.363 (0.45), 2.371 (0.43), 2.428 (0.31), 2.637 (0.42), 2.651(0.79), 2.698 (11.97), 2.969 (0.31), 2.995 (0.20), 3.207 (1.43), 3.829(2.41), 3.842 (2.28), 6.994 (0.50), 7.096 (0.61), 7.198 (0.59), 7.260(2.25), 7.278 (4.59), 7.295 (2.65), 7.729 (2.20), 8.513 (0.39), 9.493(0.31).

Example 5021-[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]ethanone

Ethyl1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate(375 mg, 766 μmol) was dissolved in tetrahydrofuran (3.0 ml, 37 mmol)under an argon atmosphere and the resulting solution was cooled to 0° C.A solution of bromo(methyl)magnesium (890 μl, 3.0 M in diethyl ether,2.7 mmol) was added dropwise and the reaction mixture was stirred 2hours at ambient temperature. Additional 3.5 equivalents ofbromo(methyl)magnesium (890 μl, 3.0 M in diethyl ether, 2.7 mmol) wereadded and it was stirred another hour. The mixture was diluted withwater and extracted with ethyl acetate (2×). The combined organic phaseswere dried over Extrelut NT3 and the residue was purified byflash-chromatography (column: SNAP Ultra 10 g, solvent: 90%dichloromethane/10% ethyl acetate to 100% ethyl acetate) to yield 61.1mg (17%) of the described product as a by-product of2-[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]propan-2-ol.

LC-MS (method 10): R_(t)=2.09 min; MS (ESIpos): m/z=460 [M+H]⁺

¹H-NMR (400 MHz, dimethylsulfoxide-d6) δ [ppm]: −0.008 (0.58), 0.008(0.60), 0.296 (1.18), 0.308 (1.25), 0.427 (1.23), 0.447 (1.24), 1.074(0.48), 1.091 (0.97), 1.109 (0.49), 1.200 (0.50), 1.276 (3.67), 1.293(3.71), 1.459 (16.00), 1.475 (1.33), 1.994 (0.42), 2.010 (6.96), 2.273(8.60), 2.283 (0.89), 2.421 (1.02), 2.435 (1.01), 2.464 (4.05), 2.639(8.80), 2.770 (0.64), 2.889 (4.72), 3.375 (0.50), 3.392 (0.48), 3.544(1.18), 3.557 (1.25), 3.565 (1.24), 3.580 (1.18), 3.834 (1.07), 3.851(1.01), 4.826 (3.29), 5.334 (0.60), 5.350 (0.58), 7.149 (1.69), 7.168(2.05), 7.171 (1.91), 7.194 (1.31), 7.212 (0.71), 7.251 (1.27), 7.274(2.31), 7.296 (1.20), 7.368 (1.51), 7.389 (1.89), 7.408 (1.03), 7.711(0.79), 7.725 (1.00), 7.746 (0.71).

Example 503

N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-[4-(methoxymethyl)-3,5-dimethyl-1H-pyrazol-1-yl]pyrimidin-4-amine

A microwave vial was charged with1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine(52.9 mg, 216 μmol) and4-chloro-6-[4-(methoxymethyl)-3,5-dimethyl-1H-pyrazol-1-yl]pyrimidine(60.0 mg, 237 μmol) and the contents were suspended in 1,4-dioxane (0.86mL). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (5.93 mg, 6.48 μmol) and XantPhos(7.49 mg, 13.0 μmol) were added and the reaction mixture was degassedagain for 1 min. Finally, sodium phenolate (27.6 mg, 237 μmol) wasadded, the vial was sealed and heated at 85° C. overnight whilevigorously shaking. After cooling to ambient temperature, the reactionmixture was filtered and concentrated. The residue was redissolved indimethylsulfoxide and purified by preparative HPLC (column: ChromatorexC18; 125*30 mm, 10 μM, flow 75 mL/min, gradient acetonitrile/water(containing 0.1% trifluoroacetic acid) 10/90 to 95/5) and further byflash column chromatography (SNAP Ultra 10 g, cyclohexane/ethyl acetategradient) to yield the desired product (44 mg, 44% yield).

LC-MS (method 10): R_(t)=2.20 min; MS (ESIpos): m/z=462 [M+H]⁺

¹H-NMR (500 MHz, dimethylsulfoxide-d6) δ [ppm]: 0.295 (2.29), 0.304(2.32), 0.425 (2.42), 0.441 (2.42), 1.161 (0.89), 1.176 (1.81), 1.183(0.73), 1.190 (1.34), 1.198 (1.02), 1.207 (0.60), 1.212 (0.60), 1.989(3.02), 2.009 (13.46), 2.184 (2.04), 2.632 (16.00), 2.664 (0.41), 3.216(11.51), 3.354 (0.51), 3.830 (2.00), 3.843 (1.91), 4.023 (0.64), 4.038(0.64), 4.250 (4.36), 7.256 (2.10), 7.274 (4.20), 7.292 (2.23), 7.719(1.34), 7.730 (1.81), 7.746 (1.24), 8.473 (0.51), 9.387 (0.48).

Example 504N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-{4-[(±)-1-(dimethylamino)-2,2,2-trifluoroethyl]-3,5-dimethyl-1H-pyrazol-1-yl}pyrimidin-4-amine(racemate)

A microwave vial was charged with1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine(5.14 mg, 21.0 μmol) and(±)-1-[1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]-2,2,2-trifluoro-N,N-dimethylethanamine(racemate, 7.00 mg, 21.0 μmol) and the contents were suspended in1,4-dioxane (0.5 mL). The reaction mixture was degassed with Ar for 3min. Tris(dibenzylideneacetone)dipalladium (580 μg, 0.63 μmol) andXantPhos (730 μg, 1.3 μmol) were added and the reaction mixture wasdegassed again for 1 min. Finally, sodium phenolate (2.68 mg, 23.1 μmol)was added, the vial was sealed and heated at 85° C. overnight whilevigorously shaking. After cooling to ambient temperature, the reactionmixture was concentrated. The residue was purified by flash columnchromatography (KP Sil 10 g, cyclohexane/ethyl acetate 95/5 to 20/80) toyield the desired product (1.9 mg, 15% yield).

LC-MS (method 11): R_(t)=1.64 min; MS (ESIneg): m/z=541 [M−H]⁻

¹H NMR (600 MHz, dimethylsulfoxide-d₆) 6 ppm: 0.30 (br d, J=2.93 Hz,2H), 0.44 (br d, J=7.89 Hz, 2H), 1.16-1.23 (m, 1H), 2.01 (s, 3H),2.16-2.29 (m, 9H), 2.70 (s, 3H), 3.84 (br s, 2H), 3.99-4.19 (m, 1H),7.21-7.36 (m, 3H), 7.70-7.78 (m, 2H), 8.34-8.69 (br s, 1H) 9.29-9.71 (brs, 1H).

Example 5056-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-[3-(6-methoxypyridin-3-yl)-1,4-dimethyl-1H-pyrazol-5-yl]pyrimidin-4-amine

In a sealed microwave tube under argon,3-(6-methoxypyridin-3-yl)-1,4-dimethyl-1H-pyrazol-5-amine (50.0 mg, 229μmol), 4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine(66.8 mg, 275 μmol), sodium phenolate (29.3 mg, 252 μmol),tris(dibenzylidenaceton)dipalladium (6.29 mg, 6.87 μmol), Xantphos (7.27mg, 13.7 μmol) were dissolved in 1,4-dioxane (1.1 ml). The reactionmixture was heated at 90° C. for 45 minutes. The cooled reaction mixturewas diluted with dichloromethane, washed with a saturated aqueoussolution of sodium hydrogen carbonate and the aqueous phase thenextracted twice with dichloromethane. The combined organic phase s weredried with sodium sulfate and concentrated in vacuo. The crude productwas purified by flash-chromatography on silica gel (Gradient 12% to 100%ethylacetate in cyclohexane, column: Biotage SNAP Ultra 10 g) and thenby preparative HPLC (Method 1) to yield 44.8 mg (100% purity, 46% yield)of the desired product.

LC-MS (Method 10): R_(t)=2.14 min; MS (ESIpos): m/z=425 [M+H]⁺

¹H-NMR (500 MHz, DIMETHYLSULFOXIDE-d6) δ [ppm]: −0.007 (1.47), 0.006(0.98), 2.008 (11.85), 2.216 (1.62), 2.648 (11.45), 3.660 (5.35), 3.894(16.00), 5.754 (1.20), 6.892 (1.51), 6.909 (1.54), 7.981 (0.62), 7.985(0.63), 7.998 (0.61), 8.003 (0.59), 8.439 (1.17), 8.443 (1.14), 9.513(0.46).

Example 506{[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]oxy}acetonitrile

A microwave vial was charged with1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine(100 mg, 408 μmol),[1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]oxylacetonitrile(118 mg, 448 μmol) and sodium phenolate (52.1 mg, 448 μmol) and thecontents were suspended in dioxane (1.3 mL). The reaction mixture wasdegassed with Ar for 3 min. Tris(dibenzylideneacetone)dipalladium (11.2mg, 12.2 μmol) and XantPhos (14.2 mg, 24.5 μmol) were added and thereaction mixture was degassed again for 1 min. The vial was sealed andheated at 85° C. overnight while vigorously shaking. After cooling toambient temperature, the reaction mixture was diluted with ethylacetate, filtered over Celite and concentrated. The residue wasredissolved in dimethylsulfoxide and purified by preparative HPLC(method 3) to yield the desired product (81 mg, 40% yield).

LC-MS (method 10): R_(t)=2.15 min; MS (ESIpos): m/z=473 [M+H]⁺

¹H-NMR (500 MHz, DIMETHYLSULFOXIDE-d6) δ [ppm]: 0.291 (1.98), 0.300(2.04), 0.423 (2.14), 0.439 (2.19), 1.167 (0.33), 1.176 (0.59), 1.182(0.59), 1.191 (0.88), 1.201 (0.54), 1.206 (0.57), 1.216 (0.28), 2.006(12.47), 2.215 (1.62), 2.363 (0.21), 2.598 (16.00), 2.637 (0.21), 3.828(1.62), 3.841 (1.57), 4.949 (4.66), 7.257 (1.80), 7.275 (3.50), 7.293(1.88), 7.345 (0.70), 7.378 (0.77), 7.463 (1.11), 7.465 (1.06), 7.477(0.67), 7.720 (1.16), 7.731 (1.55), 7.784 (0.70), 7.792 (0.59), 7.796(0.64), 7.806 (0.54), 7.811 (0.59), 7.816 (0.59), 8.472 (0.39), 9.415(0.33).

Example 5071-[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]-1,1-difluoro-2-methylpropan-2-ol

Under an argon atmosphere, ethyl[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl](difluoro)acetate(30.0 mg, 55.6 μmol) was dissolved in tetrahydrofuran and the solutioncooled to 0° C. A solution of bromido(methyl)magnesium (280 μl, 1.0 M,280 μmol) was added dropwise and the reaction mixture was stirred for 35min at ambient temperature. The reaction mixture was carefully quenchedby addition of aqueous Na₂EDTA solution (10%) and extracted with ethylacetate (3×). The combined organic extracts were dried over sodiumsulfate and concentrated. The residue was dissolved standing overnight,the organic phase was decanted and concentrated. The residue wasdissolved in tetrahydrofuran and the solution cooled to 0° C. A solutionof bromido(methyl)magnesium (280 μl, 1.0 M, 280 μmol) was added dropwiseand the reaction mixture was stirred for 20 min at ambient temperature.The reaction mixture was carefully quenched by addition of aqueousNa₂EDTA solution (10%) and extracted with ethyl acetate (3×). Thecombined organic extracts were dried over sodium sulfate andconcentrated. The residue was purified by preparative HPLC (column:Chromatorex C18; 125*30 mm, 10 μM, flow 75 mL/min, gradientacetonitrile/water (containing 0.1% trifluoroacetic acid) 10/90 to 95/5)to yield the desired product (8 mg, 26% yield).

LC-MS (method 9): R_(t)=1.15 min; MS (ESIpos): m/z=526 [M+H]⁺

¹H-NMR (600 MHz, DIMETHYLSULFOXIDE-d6) δ [ppm]: 0.298 (3.18), 0.431(3.65), 0.444 (3.68), 0.853 (0.30), 1.119 (0.44), 1.162 (1.09), 1.176(1.81), 1.188 (2.04), 1.197 (2.63), 1.219 (15.64), 1.258 (0.89), 1.299(0.36), 1.500 (0.17), 1.645 (0.23), 1.991 (1.89), 2.011 (16.00), 2.116(0.17), 2.176 (0.58), 2.254 (1.50), 2.388 (0.20), 2.618 (0.20), 2.687(13.68), 3.838 (2.24), 4.023 (0.44), 4.035 (0.44), 4.047 (0.17), 5.324(2.56), 5.762 (0.59), 7.265 (2.62), 7.279 (5.14), 7.293 (2.88), 7.731(2.51), 8.492 (0.34), 9.452 (0.30), 11.232 (0.30).

Example 5086-[4-(cyclopropylmethoxy)-3,5-dimethyl-1H-pyrazol-1-yl]-N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]pyrimidin-4-amine

A microwave vial was charged with1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine(16.0 mg, 65.2 μmol) and4-chloro-6-[4-(cyclopropylmethoxy)-3,5-dimethyl-1H-pyrazol-1-yl]pyrimidine(20.0 mg, 71.8 μmol) and the contents were suspended in dioxane (0.5mL). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (1.79 mg, 1.96 μmol) and XantPhos(2.26 mg, 3.91 μmol) were added and the reaction mixture was degassedagain for 1 min. Lastly, sodium phenolate (8.33 mg, 71.8 μmol) wasadded, the vial was sealed and heated at 85° C. overnight whilevigorously shaking. After cooling to ambient temperature, the reactionmixture was diluted with ethyl acetate, filtered and concentrated. Theresidue was redissolved in dimethylsulfoxide and purified by preparativeHPLC (method 6) to yield the desired product (2 mg, 5% yield).

LC-MS (method 11): R_(t)=1.61 min; MS (ESIpos): m/z=488 [M+H]⁺

¹H-NMR (600 MHz, DIMETHYLSULFOXIDE-d6) δ [ppm]: 0.247 (4.98), 0.261(0.90), 0.291 (2.70), 0.298 (2.77), 0.421 (2.92), 0.434 (3.01), 0.527(3.45), 0.530 (3.16), 0.537 (3.51), 0.543 (2.33), 0.550 (0.69), 1.135(1.21), 1.143 (1.25), 1.155 (0.82), 1.164 (0.59), 1.168 (0.67), 1.176(0.94), 1.181 (0.85), 1.189 (1.28), 1.197 (0.84), 1.201 (0.85), 1.233(0.40), 2.000 (16.00), 2.161 (1.42), 2.181 (11.17), 2.388 (0.25), 2.579(10.35), 2.616 (0.27), 3.509 (0.18), 3.653 (2.31), 3.664 (2.31), 3.678(3.89), 3.690 (3.62), 3.831 (1.90), 7.166 (2.91), 7.254 (2.20), 7.263(2.58), 7.266 (3.26), 7.277 (4.08), 7.292 (2.18), 7.318 (0.59), 7.331(1.29), 7.343 (0.77), 7.486 (1.55), 7.500 (2.15), 7.512 (1.22), 7.731(1.87), 8.436 (0.35), 8.656 (2.69), 9.366 (0.16).

Example 509N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-[4-(difluoromethoxy)-3,5-dimethyl-1H-pyrazol-1-yl]pyrimidin-4-amine

A microwave vial was charged with1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine(110 mg, 447 μmol) and4-chloro-6-[4-(difluoromethoxy)-3,5-dimethyl-1H-pyrazol-1-yl]pyrimidine(135 mg, 492 μmol) and the contents were suspended in dioxane (1.7 mL).The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (12.3 mg, 13.4 μmol) and XantPhos(15.5 mg, 26.8 μmol) were added and the reaction mixture was degassedagain for 1 min. Lastly, sodium phenolate (57.1 mg, 492 μmol) was added,the vial was sealed and heated at 85° C. overnight while vigorouslyshaking. After cooling to ambient temperature, the reaction mixture wasfiltered and concentrated. The residue was redissolved indimethylsulfoxide and purified by preparative HPLC (method 4) to yieldthe desired product (93 mg, 41% yield).

LC-MS (method 10): R_(t)=2.32 min; MS (ESIpos): m/z=484 [M+H]⁺

¹H-NMR (500 MHz, DIMETHYLSULFOXIDE-d6) δ [ppm]: −0.007 (0.85), 0.007(0.54), 0.292 (2.08), 0.301 (2.14), 0.424 (2.29), 0.440 (2.33), 1.163(0.25), 1.168 (0.35), 1.177 (0.66), 1.183 (0.64), 1.193 (1.00), 1.202(0.59), 1.208 (0.60), 1.217 (0.30), 1.223 (0.20), 2.008 (14.36), 2.175(1.62), 2.196 (2.64), 2.577 (16.00), 2.600 (2.14), 3.831 (1.70), 3.844(1.64), 6.873 (0.58), 6.901 (0.23), 7.020 (1.13), 7.048 (0.46), 7.166(0.58), 7.194 (0.22), 7.239 (0.77), 7.241 (0.75), 7.257 (2.14), 7.261(1.37), 7.275 (4.36), 7.292 (2.16), 7.320 (0.19), 7.335 (0.35), 7.350(0.22), 7.487 (0.42), 7.502 (0.48), 7.519 (0.28), 7.720 (1.19), 7.732(1.63), 7.747 (1.12), 8.491 (0.37), 8.707 (0.63), 8.709 (0.61), 9.454(0.29).

Example 510N-{1-(cyclopropylmethyl)-3-[6-(difluoromethyl)pyridin-3-yl]-4-methyl-1H-pyrazol-5-yl}-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged with1-(cyclopropylmethyl)-3-[6-(difluoromethyl)pyridin-3-yl]-4-methyl-1H-pyrazol-5-amine(100 mg, 359 μmol) and4-chloro-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (94.3 mg,395 μmol) and the contents were suspended in dioxane (1.5 mL). Thereaction mixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (9.87 mg, 10.8 μmol) and XantPhos(12.5 mg, 21.6 μmol) were added and the reaction mixture was degassedagain for 1 min. Finally, sodium phenolate (45.9 mg, 395 μmol) was addedand the vial was sealed and heated at 85° C. overnight while vigorouslyshaking. After cooling to ambient temperature, the reaction mixture wasfiltered and concentrated. The residue was redissolved indimethylsulfoxide and purified by preparative HPLC (method 3) to yieldthe desired product (47.6 mg, 28% yield).

LC-MS (method 10): R_(t)=2.10 min; MS (ESIpos): m/z=481 [M+H]⁺

¹H-NMR (500 MHz, DIMETHYLSULFOXIDE-d6) δ [ppm]: −0.007 (0.58), 0.312(2.35), 0.322 (2.47), 0.332 (0.71), 0.439 (2.47), 0.455 (2.54), 1.203(0.68), 1.209 (0.66), 1.219 (1.05), 1.228 (0.61), 1.233 (0.62), 2.071(16.00), 2.187 (2.44), 3.316 (15.94), 3.877 (2.10), 3.890 (2.03), 6.899(1.56), 7.009 (3.41), 7.119 (1.36), 7.773 (2.37), 7.790 (2.51), 8.273(1.11), 8.289 (1.06), 8.453 (0.66), 9.017 (2.11), 9.420 (0.60).

Example 5116-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-{1-(cyclopropylmethyl)-3-[6-(difluoromethyl)pyridin-3-yl]-4-methyl-1H-pyrazol-5-yl}pyrimidin-4-amine

A microwave vial was charged with1-(cyclopropylmethyl)-3-[6-(difluoromethyl)pyridin-3-yl]-4-methyl-1H-pyrazol-5-amine(100 mg, 359 μmol) and4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (96.1 mg,395 μmol) and the contents were suspended in dioxane (1.5 mL). Thereaction mixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (9.87 mg, 10.8 μmol) and XantPhos(12.5 mg, 21.6 μmol) were added and the reaction mixture was degassedagain for 1 min. Lastly, sodium phenolate (45.9 mg, 395 μmol) was added,the vial was sealed and heated at 85° C. overnight while vigorouslyshaking. After cooling to ambient temperature, the reaction mixture wasfiltered and concentrated. The residue was redissolved indimethylsulfoxide and purified by preparative HPLC (method 4) to yieldthe desired product (78 mg, 45% yield).

LC-MS (method 10): R_(t)=2.41 min; MS (ESIpos): m/z=485 [M+H]⁺

¹H-NMR (500 MHz, DIMETHYLSULFOXIDE-d6) δ [ppm]: −0.006 (0.50), 0.007(0.27), 0.314 (2.03), 0.324 (2.10), 0.441 (2.14), 0.457 (2.18), 1.191(0.22), 1.196 (0.32), 1.206 (0.60), 1.211 (0.58), 1.221 (0.90), 1.231(0.53), 1.236 (0.55), 1.245 (0.27), 1.251 (0.18), 2.074 (13.29), 2.216(1.75), 2.264 (0.22), 2.650 (16.00), 3.880 (1.74), 3.894 (1.68), 6.899(1.32), 7.009 (2.88), 7.119 (1.16), 7.774 (2.03), 7.790 (2.16), 8.273(0.93), 8.289 (0.88), 8.503 (0.41), 9.017 (1.77), 9.528 (0.31).

Example 5121-[6-({1-(cyclopropylmethyl)-3-[6-(difluoromethyl)pyridin-3-yl]-4-methyl-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3,5-dimethyl-1H-pyrazole-4-carbonitrile

A microwave vial was charged with1-(cyclopropylmethyl)-3-[6-(difluoromethyl)pyridin-3-yl]-4-methyl-1H-pyrazol-5-amine(100 mg, 359 μmol) and1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carbonitrile (120mg, 77% purity, 395 μmol) and the contents were suspended in dioxane(1.5 mL). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (9.87 mg, 10.8 μmol) and XantPhos(12.5 mg, 21.6 μmol) were added and the reaction mixture was degassedagain for 1 min. Lastly, sodium phenolate (45.9 mg, 395 μmol) was added,the vial was sealed and heated at 85° C. overnight while vigorouslyshaking. After cooling to ambient temperature, the reaction mixture wasfiltered and concentrated. The residue was redissolved indimethylsulfoxide and purified by preparative HPLC (method 3) to yieldthe desired product (11 mg, 6% yield).

LC-MS (method 10): R_(t)=2.07 min; MS (ESIpos): m/z=476 [M+H]⁺

¹H-NMR (500 MHz, DIMETHYLSULFOXIDE-d6) δ [ppm]: −0.007 (0.83), 0.007(0.48), 0.311 (2.33), 0.320 (2.38), 0.440 (2.52), 0.456 (2.56), 1.191(0.39), 1.200 (0.72), 1.206 (0.70), 1.216 (1.06), 1.225 (0.65), 1.231(0.65), 1.240 (0.33), 1.647 (0.52), 2.071 (15.87), 2.337 (1.50), 2.799(16.00), 3.880 (1.78), 3.893 (1.72), 6.898 (1.60), 7.008 (3.50), 7.118(1.39), 7.371 (0.41), 7.384 (0.41), 7.395 (0.43), 7.773 (2.37), 7.789(2.50), 8.271 (1.03), 8.286 (0.97), 8.548 (0.34), 9.013 (1.94), 9.630(0.22).

Example 5134-[5-{[6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-3-yl]cubane-1-carbonitrile

A microwave vial was charged with4-[5-amino-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-3-yl]cubane-1-carbonitrile(60.0 mg, 216 μmol) and4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (57.6 mg,237 μmol) and the contents were suspended in dioxane (1.2 mL). Thereaction mixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (5.92 mg, 6.47 μmol) and XantPhos(7.48 mg, 12.9 μmol) were added and the reaction mixture was degassedagain for 1 min. Lastly, sodium phenolate (27.5 mg, 237 μmol) was addedand the vial was sealed and heated at 85° C. overnight while vigorouslyshaking. After cooling to ambient temperature, the reaction mixture wasfiltered and concentrated. The residue was redissolved indimethylsulfoxide and purified by preparative HPLC (method 1) to yieldthe desired product (28 mg, 27% yield).

LC-MS (method 11): R_(t)=1.55 min; MS (ESIpos): m/z=485 [M+H]⁺

¹H NMR (500 MHz, DIMETHYLSULFOXIDE-d₆) δ ppm: 0.18-0.27 (m, 2H),0.35-0.43 (m, 2H), 1.07-1.17 (m, 1H), 1.77 (s, 3H), 2.22 (s, 3H), 2.63(s, 3H), 3.72 (d, J=6.86 Hz, 2H), 4.25-4.35 (m, 3H), 4.36-4.45 (m, 3H),8.47 (br s, 1H), 9.18-9.60 (br s, 1H).

Example 5144-[1-(cyclopropylmethyl)-5-{[6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-4-methyl-1H-pyrazol-3-yl]cubane-1-carbonitrile

A microwave vial was charged with4-[5-amino-1-(cyclopropylmethyl)-4-methyl-1H-pyrazol-3-yl]cubane-1-carbonitrile(50.0 mg, 180 μmol) and4-chloro-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (47.2 mg,198 μmol) and the contents were suspended in dioxane (1.0 mL). Thereaction mixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (4.93 mg, 5.39 μmol) and XantPhos(6.24 mg, 10.8 μmol) were added and the reaction mixture was degassedagain for 1 min. Lastly, sodium phenolate (22.9 mg, 198 μmol) was added,the vial was sealed and heated at 85° C. overnight while vigorouslyshaking. After cooling to ambient temperature, the reaction mixture wasfiltered and concentrated. The residue was redissolved indimethylsulfoxide and purified by preparative HPLC (method 1) to yieldthe desired product (28 mg, 33% yield).

LC-MS (method 11): R_(t)=1.39 min; MS (ESIpos): m/z=481 [M+H]⁺

¹H NMR (500 MHz, DIMETHYLSULFOXIDE-d₆) δ ppm: 0.22 (q, J=4.83 Hz, 2H),0.36-0.41 (m, 2H), 1.08-1.16 (m, 1H), 1.77 (s, 3H), 2.18 (s, 3H), 2.53(s, 3H), 3.67-3.73 (m, 5H), 4.29-4.33 (m, 3H), 4.38-4.43 (m, 3H), 8.42(br s, 1H), 9.24 (br s, 1H).

Example 5152-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,4-dimethyl-2,4,5,6-tetrahydrocyclopenta[c]pyrazol-4-ol

Obtained from separation of the enantiomers of a racemic sample of2-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,4-dimethyl-2,4,5,6-tetrahydrocyclopenta[c]pyrazol-4-ol(racemate 293 mg dissolved in ethanol/acetonitrile 5:2, 7 mL) bypreparative HPLC (Daicel Chiralpak IA 5 μm, 250×20 mm, 50° C., flow: 15mL/min, isocratic ethanol/n-heptane 80/20 +0.2% diethylamine, injectionsof 0.15 mL every 13 min) to yield the title compound as the firsteluting enantiomer (133 mg, 45% from racemate). As partial eliminationwas observed during concentration, the compound was repurified by flashcolumn chromatography (SNAP Ultra 10 g, cyclohexane/ethyl acetategradient 80/20 to 0/100) to yield the desired product (70 mg, 24% yieldbased on racemate).

LC (Daicel Chiralpak IA-3 3 μm, 50 mm×4.6 mm, 1 mL/min n-heptane/EtOH80/20+0.2% diethylamine) R_(t)=1.42 min, enantiomeric excess=93.4%

LC-MS (method 11): R_(t)=1.33 min; MS (ESIneg): m/z=472 [M−H]⁻

¹H-NMR (500 MHz, DIMETHYLSULFOXIDE-d6) δ [ppm]: −0.120 (0.41), −0.007(4.38), 0.006 (3.18), 0.116 (0.41), 0.285 (1.47), 0.293 (1.52), 0.415(1.65), 0.430 (1.68), 1.167 (0.48), 1.175 (0.53), 1.181 (0.72), 1.189(0.47), 1.196 (0.46), 1.470 (5.78), 1.988 (0.36), 2.006 (13.90), 2.304(1.23), 2.362 (0.22), 2.519 (0.59), 2.523 (0.55), 2.635 (0.34), 2.655(16.00), 2.690 (0.37), 3.828 (1.58), 3.842 (1.53), 5.027 (2.54), 7.255(1.98), 7.259 (0.77), 7.273 (4.05), 7.287 (0.82), 7.291 (2.12), 7.724(1.08), 7.736 (1.45), 7.752 (1.03), 8.469 (0.43), 9.359 (0.53).

Example 5162-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,4-dimethyl-2,4,5,6-tetrahydrocyclopenta[c]pyrazol-4-ol

Obtained from separation of the enantiomers of a racemic sample of2-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,4-dimethyl-2,4,5,6-tetrahydrocyclopenta[c]pyrazol-4-ol(racemate 293 mg dissolved in ethanol/acetonitrile 5:2, 7 mL) bypreparative HPLC (Daicel Chiralpak IA 5 μm, 250×20 mm, 50° C., flow: 15mL/min, isocratic ethanol/n-heptane 80/20+0.2% diethylamine, injectionsof 0.15 mL every 13 min) to yield the title compound as the secondeluting enantiomer (130 mg, 44% from racemate). As partial eliminationwas observed during concentration, the compound was repurified by flashcolumn chromatography (SNAP Ultra 10g, cyclohexane/ethyl acetategradient 80/20 to 0/100) to yield the desired product (60 mg, 20% yieldbased on racemate).

LC (Daicel Chiralpak IA-3 3 μm, 50 mm×4.6 mm, 1 mL/min n-heptane/EtOH80/20+0.2% diethylamine) R_(t)=2.72 min, enantiomeric excess=90.2%

LC-MS (method 11): R_(t)=1.32 min; MS (ESIpos): m/z=474 [M+H]⁺

¹H-NMR (500 MHz, DIMETHYLSULFOXIDE-d6) δ [ppm]: −0.120 (0.29), −0.007(3.73), 0.006 (1.95), 0.117 (0.29), 0.285 (1.69), 0.293 (1.71), 0.415(1.85), 0.431 (1.87), 1.161 (0.37), 1.167 (0.56), 1.175 (0.73), 1.182(0.79), 1.189 (0.60), 1.196 (0.51), 1.398 (0.21), 1.470 (6.30), 1.988(0.67), 2.007 (14.73), 2.304 (1.39), 2.362 (0.16), 2.523 (0.51), 2.655(16.00), 2.689 (0.41), 3.829 (1.79), 3.842 (1.71), 5.028 (2.72), 7.255(2.08), 7.273 (4.20), 7.291 (2.19), 7.725 (1.24), 7.737 (1.65), 7.753(1.15), 8.467 (0.49), 9.361 (0.58).

Example 517N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-{3,5-dimethyl-4-[2-(trifluoromethyl)-1,3-dioxolan-2-yl]-1H-pyrazol-1-yl}pyrimidin-4-amine

Under an argon atmosphere,4-chloro-6-{3,5-dimethyl-4-[2-(trifluoromethyl)-1,3-dioxolan-2-yl]-1H-pyrazol-1-yl}pyrimidine(1.50 g, 90% purity, 3.87 mmol) and1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine(1.14 g, 4.65 mmol) were suspended in dioxane (25 mL). The reactionmixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (124 mg, 135 μmol) and XantPhos(146 mg, 252 μmol) were added and the reaction mixture was degassedagain for 1 min. Lastly, sodium phenolate (517 mg, 4.45 mmol) was addedand the reaction mixture heated at 85° C. overnight while vigorouslystirring. After cooling to ambient temperature, the reaction mixture wasdiluted with water and extracted with ethyl acetate (2×). The combinedorganic extracts were dried over sodium sulfate and concentrated. Theresidue was purified by flash column chromatography (SNAP Ultra 50 g,cyclohexane/ethyl acetate gradient 90/10 to 20/80) to yield the desiredproduct (1.24 g, 57% yield).

LC-MS (method 11): R_(t)=1.61 min; MS (ESIpos): m/z=558 [M+H]⁺

¹H-NMR (400 MHz, DIMETHYLSULFOXIDE-d6) δ [ppm]: −0.149 (0.16), −0.008(1.22), 0.008 (1.31), 0.145 (0.16), 0.290 (0.95), 0.300 (1.02), 0.423(0.92), 0.442 (1.02), 1.192 (0.41), 1.398 (16.00), 2.004 (5.83), 2.254(0.90), 2.327 (0.86), 2.366 (0.40), 2.523 (2.64), 2.669 (0.92), 2.674(0.71), 2.710 (0.49), 2.729 (5.38), 3.568 (0.20), 3.825 (0.82), 3.842(0.80), 4.087 (1.05), 4.223 (1.22), 4.240 (0.32), 7.250 (0.90), 7.272(1.83), 7.294 (0.98), 7.708 (0.61), 7.723 (0.80), 7.744 (0.56), 8.500(0.21), 9.459 (0.17).

Example 5181-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-ylmethyl carbonate

A microwave vial was charged with1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl methyl carbonate(100 mg, 100% purity, 354 μmol) and1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine(95.5 mg, 389 μmol) and and the contents were suspended in dioxane (1.1mL). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (6.10 mg, 10.6 μmol) and XantPhos(12.3 mg, 21.2 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was heated at 85° C. when sodium phenolate(45.2 mg, 389 μmol) was added. The vial was sealed and heated at 85° C.overnight while vigorously shaking. After cooling to ambienttemperature, the reaction mixture was diluted with aqueous saturatedsodium hydrogencarbonate solution and extracted with ethyl acetate (2×).The combined organic extracts were washed with brine, dried over sodiumsulfate and concentrated. The residue was redissolved indimethylsulfoxide and purified by preparative HPLC (method 4) to yieldthe desired product (12 mg, 7% yield).

LC-MS (method 11): R_(t)=1.49 min; MS (ESIpos): m/z=492 [M+H]⁺

¹H NMR (400 MHz, DIMETHYLSULFOXIDE-d₆) δ ppm: 0.25-0.35 (m, 2H),0.39-0.48 (m, 2H), 1.15-1.25 (m, 1H), 2.01 (s, 3H), 2.06-2.18 (br s,3H), 2.53 (s, 3H), 3.81-3.88 (m, 5H), 7.24-7.32 (m, 2H), 7.66-7.82 (m,2H), 8.41-8.62 (br s, 1H), 9.36-9.55 (br s, 1H).

Example 5191-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-ylmethylcarbamate

A microwave vial was charged with1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl methylcarbamate(100 mg, 100% purity, 355 μmol) and1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine(95.8 mg, 390 μmol) and and the contents were suspended in dioxane (1.1mL). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (6.12 mg, 10.6 p,mol) and XantPhos(12.3 mg, 21.3 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was heated at 85° C. when sodium phenolate(45.3 mg, 390 μmol) was added. The vial was sealed and heated at 85° C.overnight while vigorously shaking. After cooling to ambienttemperature, the reaction mixture was diluted with aqueous saturatedsodium hydrogencarbonate solution and extracted with ethyl acetate (2×).The combined organic extracts were washed with brine, dried over sodiumsulfate and concentrated. The residue was redissolved indimethylsulfoxide and purified by preparative HPLC (method 3) to yieldthe desired product (14 mg, 7% yield).

LC-MS (method 11): R_(t)=1.34 min; MS (ESIpos): m/z=491 [M+H]⁺

¹H-NMR (400 MHz, DIMETHYLSULFOXIDE-d6) δ [ppm]: −0.149 (0.52), −0.008(4.20), 0.008 (4.20), 0.146 (0.54), 0.289 (2.45), 0.302 (2.70), 0.423(2.53), 0.442 (2.66), 1.191 (1.08), 1.647 (1.33), 2.009 (15.09), 2.065(2.74), 2.328 (0.67), 2.366 (0.69), 2.476 (16.00), 2.665 (7.00), 2.676(6.88), 2.710 (0.64), 2.794 (0.42), 3.830 (2.12), 3.845 (2.04), 7.252(2.45), 7.274 (4.84), 7.296 (2.60), 7.368 (1.00), 7.385 (0.96), 7.397(1.21), 7.724 (2.62), 8.467 (0.69), 9.405 (0.62).

Example 5201-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yldimethylcarbamate

A microwave vial was charged with1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yldimethylcarbamate (100 mg, 100% purity, 338 μmol) and1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-amine(91.2 mg, 372 μmol) and and the contents were suspended in dioxane (1.1mL). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (5.83 mg, 10.1 μmol) and XantPhos(11.7 mg, 20.3 μmol) were added and the reaction mixture was degassedagain for 1 min. The vial was heated at 85° C. when sodium phenolate(43.2 mg, 372 μmol) was added. The vial was sealed and heated at 85° C.overnight while vigorously shaking. After cooling to ambienttemperature, the reaction mixture was diluted with aqueous saturatedsodium hydrogencarbonate solution and extracted with ethyl acetate (2×).The combined organic extracts were washed with brine, dried over sodiumsulfate and concentrated. The residue was redissolved in acetonitrileand purified by preparative HPLC (column: Chromatorex C18; 125*30 mm, 10μM, flow 75 mL/min, gradient acetonitrile/water (containing 0.1%trifluoroacetic acid) 10/90 to 95/5) and further by flash columnchromatography (SNAP Ultra 10 g, cyclohexane/ethyl acetate gradient90/10 to 20/80) to yield the desired product (61 mg, 35% yield).

LC-MS (method 10): R_(t)=2.20 min; MS (ESIpos): m/z=505 [M+H]⁺

¹H-NMR (400 MHz, DIMETHYLSULFOXIDE-d6) δ [ppm]: 0.304 (2.88), 0.422(2.71), 0.442 (2.88), 1.193 (1.22), 1.398 (1.90), 2.009 (16.00), 2.068(2.92), 2.328 (1.86), 2.366 (0.75), 2.523 (5.63), 2.669 (2.00), 2.711(0.68), 2.919 (8.95), 3.067 (9.05), 3.830 (2.24), 3.846 (2.27), 7.252(2.44), 7.274 (5.08), 7.296 (2.78), 7.732 (2.07), 8.468 (0.85), 9.407(0.64).

Example 5216-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-{1-(2-methoxyethyl)-4-methyl-3-[4-(methylamino)phenyl]-1H-pyrazol-5-yl}pyrimidin-4-amine

In a sealed microwave tube under argon,1-(2-methoxyethyl)-4-methyl-3-[4-(methylamino)phenyl]-1H-pyrazol-5-amine(50.0 mg, 192 μmol),4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (56.0 mg,230 μmol), sodium phenolate (24.5 mg, 211 μmol),tris(dibenzylidenaceton)dipalladium (5.28 mg, 5.76 μmol), Xantphos (6.09mg, 11.5 μmol) were dissolved in 1,4-dioxane (1.0 ml). The reactionmixture was heated at 90° C. for 45 minutes. The cooled reaction mixturewas diluted with ethylacetate, washed with a saturated aqueous solutionof sodium bicarbonate and the aqueous phase then extracted twice withethylacetate. The combined organic phases were dried with sodium sulfateand concentrated in vacuo. The crude product was purified by bypreparative HPLC (Method 19) and then flash-chromatography on silica gel(gradient of ethylacetate in cyclohexane, column: Biotage SNAP Ultra) toyield 38.6 mg (100% purity, 43% yield) of the desired product.

LC-MS (Method 9): R_(t)=1.14 min; MS (ESIneg): m/z=465 [M−H]⁻

¹H-NMR (500 MHz, DMSO-d6) δ [ppm]: 1.954 (15.46), 2.197 (1.54), 2.643(16.00), 2.700 (8.26), 2.710 (8.15), 3.133 (2.50), 3.620 (1.54), 3.631(3.04), 3.643 (1.57), 4.061 (0.87), 5.738 (0.75), 5.748 (0.75), 6.585(3.65), 6.602 (3.76), 7.425 (1.65), 7.441 (1.62), 8.497 (0.41), 9.346(0.80).

Example 522N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-(5-propyl-5,6-dihydropyrrolo[3,4-c]pyrazol-1(4H)-yl)pyrimidin-4-amine

ToN-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-(5,6-dihydropyrrolo[3,4-c]pyrazol-1(4H)-yl)pyrimidin-4-amine(23.8 mg, 55.3 μmol) and propanal (4.0 μl, 55 μmol) in tetrahydrofuran(500 μl) under an atmosphere of argon was added sodiumtriacetoxyborhydride (16.4 mg, 77.4 μmol) and the reaction stirredovernight at room temperature. To the reaction was then added sodiumtriacetoxyborhydride (16.4 mg, 77.4 μmol), propanal (20 μl, 275 μmol)and 2 drops of acetic acid and the reaction then stirred overnight atroom temperature. The reaction was quenched with a saturated aqueoussolution of ammonium chloride, extracted with ethylacetate and theorganic phase then washed with a saturated aqueous solution of sodiumbicarbonate, dried with sodium sulfate and concentrated in vacuo. Thecrude product was purified by preparative TLC (10:1dichloromethane:Me0H) to yield 22.9 mg (100% purity, 88% yield) of thedesired product.

LC-MS (Method 10): R_(t)=1.43 min; MS (ESIpos): m/z=473 [M+H]⁺

¹H-NMR (500 MHz, DMSO-d6) δ [ppm]: 0.288 (3.03), 0.412 (3.15), 0.427(3.10), 0.897 (4.60), 0.912 (8.68), 0.926 (4.37), 1.181 (1.27), 1.234(1.94), 1.479 (1.60), 1.493 (2.74), 1.508 (2.64), 1.523 (1.39), 2.006(16.00), 2.076 (0.54), 2.676 (2.32), 2.691 (3.65), 2.705 (2.17), 3.689(3.60), 3.846 (2.72), 4.127 (5.05), 7.258 (2.44), 7.276 (4.65), 7.293(2.59), 7.561 (0.54), 7.735 (2.90), 8.464 (0.58), 9.527 (0.62).

Example 523N-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-(5-propyl-5,6-dihydropyrrolo[3,4-c]pyrazol-2(4H)-yl)pyrimidin-4-amine

ToN-[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]-6-(5,6-dihydropyrrolo[3,4-c]pyrazol-2(4H)-yl)pyrimidin-4-amine(23.3 mg, 54.1 μmol) and propanal (3.9 μl, 54 μmol) in tetrahydrofuran(500 μl) under an atmosphere of argon was added sodiumtriacetoxyborhydride (16.1 mg, 75.8 μmol) and the reaction stirredovernight at room temperature. To the reaction was then added sodiumtriacetoxyborhydride (16.4 mg, 77.4 μmol), propanal (20 μl, 275 μmol)and 2 drops of acetic acid and the reaction then stirred overnight atroom temperature. The reaction was quenched with a saturated aqueoussolution of ammonium chloride, extracted with ethylacetate and theorganic phase then washed with a saturated aqueous solution of sodiumbicarbonate, dried with sodium sulfate and concentrated in vacuo. Thecrude product was purified by preparative TLC (10:1dichloromethane:MeOH) to yield 16.2 mg (100% purity, 63% yield) of thedesired product.

LC-MS (Method 10): R_(t)=1.38 min; MS (ESIneg): m/z=471 [M−H]⁻

¹H-NMR (500 MHz, DMSO-d6) δ [ppm]: 0.285 (1.91), 0.410 (2.15), 0.425(2.10), 0.889 (2.29), 0.903 (4.20), 0.918 (2.25), 1.179 (0.86), 1.231(1.16), 1.497 (1.32), 2.011 (16.00), 2.659 (1.67), 3.672 (4.33), 3.833(2.06), 7.258 (1.99), 7.276 (3.96), 7.293 (2.09), 7.742 (1.86), 8.252(4.32), 8.473 (0.32), 9.475 (0.48).

Example 5246-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]-N-[3-(4-fluorophenyl)-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-yl]pyrimidin-4-amine

In a sealed microwave tube under argon,3-(4-fluorophenyl)-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-amine (50.0mg, 201 μmol),4-chloro-6-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidine(66.6 mg, 241 μmol), sodium phenolate (25.6 mg, 221 μmol),tris(dibenzylidenaceton)dipalladium (5.51 mg, 6.02 μmol), Xantphos (6.36mg, 12.0 μmol) were dissolved in 1,4-dioxane (1.0 ml). The reactionmixture was heated at 90° C. for 45 minutes. The cooled reaction mixturewas purified directly by flash-chromatography on silica gel (gradient2:1 to 1:1 cyclohexane:ethyl acetate, column: Biotage SNAP Ultra) toyield 46.8 mg (100% purity, 48% yield) of the desired product.

LC-MS (Method 10): R_(t)=2.44 min; MS (ESIpos): m/z=490 [M+H]⁺

¹H-NMR (500 MHz, DMSO-d6) δ [ppm]: 2.006 (16.00), 2.298 (1.65), 2.755(7.55), 3.144 (3.16), 3.649 (1.81), 3.660 (3.48), 3.671 (1.83), 4.117(1.12), 7.257 (2.11), 7.274 (4.19), 7.292 (2.23), 7.714 (1.33), 7.726(1.79), 7.741 (1.23), 8.554 (0.44), 9.529 (0.57).

Example 5256-(3,5-dimethyl-1H-pyrazol-1-yl)-N-[3-(4-fluorophenyl)-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-yl]pyrimidin-4-amine

In a sealed microwave tube under argon,3-(4-fluorophenyl)-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-amine (50.0mg, 201 μmol), 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (50.2mg, 241 μmol), sodium phenolate (25.6 mg, 221 μmol),tris(dibenzylidenaceton)dipalladium (5.51 mg, 6.02 μmol), Xantphos (6.36mg, 12.0 μmol) were dissolved in 1,4-dioxane (1.0 ml). The reactionmixture was heated at 90° C. for 45 minutes. The cooled reaction mixturewas purified directly by flash-chromatography on silica gel (gradient2:1 to 1:1 cyclohexane:ethyl acetate, column: Biotage SNAP Ultra) toyield 31.3 mg (100% purity, 37% yield) of the desired product.

LC-MS (Method 10): R_(t)=2.14 min; MS (ESIpos): m/z=422 [M+H]⁺

¹H-NMR (500 MHz, DMSO-d6) δ [ppm]: 2.005 (16.00), 2.167 (3.34), 2.629(14.36), 3.150 (7.07), 3.651 (2.24), 3.663 (4.46), 3.674 (2.30), 4.112(1.64), 6.138 (2.81), 7.257 (2.22), 7.275 (4.40), 7.292 (2.33), 7.718(1.62), 7.729 (2.12), 7.745 (1.46), 8.467 (0.97), 9.316 (2.53).

Example 526N-[3-(4-fluorophenyl)-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-yl]-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

In a sealed microwave tube under argon,3-(4-fluorophenyl)-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-amine (50.0mg, 201 μmol),4-chloro-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (57.4 mg,241 μmol), sodium phenolate (25.6 mg, 221 μmol),tris(dibenzylidenaceton)dipalladium (5.51 mg, 6.02 μmol), Xantphos (6.36mg, 12.0 μmol) were dissolved in 1,4-dioxane (1.0 ml). The reactionmixture was heated at 90° C. for 45 minutes. The cooled reaction mixturewas purified directly by flash-chromatography on silica gel (gradient2:1 to 1:1 cyclohexane:ethyl acetate, column: Biotage SNAP Ultra) toyield 45.7 mg (100% purity, 50% yield) of the desired product.

LC-MS (Method 10): R_(t)=2.13 min; MS (ESIpos): m/z=452 [M+H]⁺

¹H-NMR (500 MHz, DMSO-d6) δ [ppm]: 1.525 (0.57), 2.000 (16.00), 2.177(2.85), 3.149 (6.83), 3.648 (1.99), 3.660 (4.04), 3.671 (2.19), 3.697(10.54), 4.110 (1.42), 7.257 (1.91), 7.274 (3.94), 7.292 (2.14), 7.716(1.39), 7.728 (1.89), 7.744 (1.37), 8.451 (0.86), 9.304 (1.98).

Example 5276-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]-N-[3-(4-fluorophenyl)-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-yl]pyrimidin-4-amine

In a sealed microwave tube under argon,3-(4-fluorophenyl)-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-amine (50.0mg, 201 μmol),4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (58.9mg, 241 μmol), sodium phenolate (25.6 mg, 221 μmol),tris(dibenzylidenaceton)dipalladium (5.51 mg, 6.02 μmol), Xantphos (6.36mg, 12.0 μmol) were dissolved in 1,4-dioxane (1.0 ml). The reactionmixture was heated at 90° C. for 45 minutes. The cooled reaction mixturewas purified directly by flash-chromatography on silica gel (gradient2:1 to 1:1 cyclohexane:ethyl acetate, column: Biotage SNAP Ultra) toyield 58.5 mg (100% purity, 64% yield) of the desired product.

LC-MS (Method 10): R_(t)=2.22 min; MS (ESIpos): m/z=458 [M+H]⁺

¹H-NMR (500 MHz, DMSO-d6) δ [ppm]: 2.009 (16.00), 2.277 (1.64), 3.137(2.46), 3.649 (1.96), 3.660 (3.71), 3.671 (1.97), 4.118 (1.15), 6.779(1.98), 7.260 (1.96), 7.278 (3.80), 7.296 (2.09), 7.714 (1.79), 7.736(1.61), 7.822 (2.70), 7.931 (1.19), 8.502 (0.48), 9.503 (0.83).

Example 528 ethyl1-(6-{[3-(4-fluorophenyl)-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

In a sealed microwave tube under argon,3-(4-fluorophenyl)-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-amine (100mg, 401 μmol), ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (135mg, 481 μmol), sodium phenolate (51.2 mg, 441 μmol),tris(dibenzylidenaceton)dipalladium (11.0 mg, 12.0 μmol), Xantphos (12.7mg, 24.1 μmol) were dissolved in 1,4-dioxane (2.0 ml). The reactionmixture was heated at 90° C. for 45 minutes. The cooled reaction mixturewas purified directly by flash-chromatography on silica gel (gradient2:1 to 1:1 cyclohexane:ethyl acetate, column: Biotage SNAP Ultra) toyield 110 mg (100% purity, 56% yield) of the desired product.

LC-MS (Method 10): R_(t)=2.29 min; MS (ESIpos): m/z=494 [M+H]⁺

¹H-NMR (500 MHz, DMSO-d6) δ [ppm]: 1.290 (3.34), 1.304 (6.43), 1.318(3.18), 2.008 (16.00), 2.368 (2.06), 2.905 (11.73), 3.146 (3.49), 3.651(2.03), 3.662 (3.88), 3.673 (2.06), 4.116 (1.39), 4.232 (1.07), 4.246(2.94), 4.260 (2.89), 4.274 (1.01), 7.256 (2.17), 7.274 (4.38), 7.292(2.38), 7.715 (1.47), 7.727 (2.02), 7.743 (1.44), 8.544 (0.54), 9.493(0.86).

Example 529N-[1-(cyclopropylmethyl)-4-methyl-3-(6-methylpyridin-3-yl)-1H-pyrazol-5-yl]-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

In a sealed microwave tube under argon,1-(cyclopropylmethyl)-4-methyl-3-(6-methylpyridin-3-yl)-1H-pyrazol-5-amine(60.0 mg, 248 μmol), 4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine(56.8 mg, 272 μmol), (31.6 mg, 272 μmol), (6.80 mg, 7.43 μmol), (7.85mg, 14.9 μmol) were dissolved in 1,4-dioxane (1.2 ml). The reactionmixture was heated at 90° C. for 30 minutes. The cooled reaction mixturewas diluted with ethylacetate, washed with a saturated aqueous solutionof sodium hydrogen carbonate and the aqueous phase then extracted twicewith ethylacetate. The combined organic phases were dried with sodiumsulfate and concentrated in vacuo. The crude product was purified byflash-chromatography on silica gel (Gradient 20% to 100% ethylacetate incyclohexane, column: Biotage SNAP Ultra 10 g) to yield the desiredproduct 53.9 mg (100% purity, 53% yield).

LC-MS (Method 10): R_(t)=1.45 min; MS (ESIpos): m/z=415 [M+H]⁺

¹H-NMR (500 MHz, CHLOROFORM-d) δ [ppm]: 0.328 (0.64), 0.338 (2.58),0.350 (2.58), 0.359 (0.73), 0.543 (0.78), 0.553 (2.09), 0.555 (2.10),0.559 (1.02), 0.569 (2.21), 0.571 (2.01), 0.581 (0.62), 1.270 (0.53),1.272 (0.49), 1.277 (0.51), 1.286 (0.88), 1.296 (0.48), 1.301 (0.47),1.302 (0.47), 2.110 (16.00), 2.219 (13.40), 2.601 (15.07), 2.676(11.82), 2.678 (11.67), 3.940 (3.06), 3.954 (3.01), 5.968 (3.03), 6.615(0.47), 6.872 (0.69), 7.218 (1.99), 7.234 (2.08), 7.950 (1.68), 7.955(1.68), 7.966 (1.58), 7.971 (1.59), 8.514 (4.06), 8.516 (3.98), 8.851(2.11), 8.855 (2.07).

Example 530

N-[1,4-dimethyl-3-(6-methylpyridin-3-yl)-1H-pyrazol-5-yl]-6-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidin-4-amine

In a sealed microwave tube under argon,1,4-dimethyl-3-(6-methylpyridin-3-yl)-1H-pyrazol-5-amine (45.0 mg, 222μmol),4-chloro-6-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidine(73.9 mg, 267 μmol), sodium phenolate (28.4 mg, 245 μmol),tris(dibenzylidenaceton)dipalladium (6.11 mg, 6.67 μmol), Xantphos (7.06mg, 13.3 μmol) were dissolved in 1,4-dioxane (1.1 ml). The reactionmixture was heated at 90° C. for 45 minutes. The cooled reaction mixturewas diluted with dichloromethane, washed with a saturated aqueoussolution of sodium hydrogen carbonate and the aqueous phase thenextracted twice with dichloromethane. The combined organic phases weredried with sodium sulfate and concentrated in vacuo. The crude productwas purified by flash-chromatography on silica gel (Gradient 25% to 100%ethylacetate in cyclohexane, column: Biotage SNAP Ultra 10 g) and thenrecrystallized from acetonitrile to yield 49.7 mg (100% purity, 50%yield) of the desired product.

LC-MS (Method 9): R_(t)=0.84 min; MS (ESIpos): m/z=443 [M+H]⁺

¹H-NMR (500 MHz, DMSO-d6) δ [ppm]: 1.161 (1.11), 1.175 (2.26), 1.190(1.15), 1.989 (4.22), 2.029 (16.00), 2.309 (1.59), 2.759 (6.00), 3.351(0.41), 3.680 (6.11), 4.023 (0.93), 4.037 (0.93), 7.316 (1.78), 7.332(1.85), 7.925 (0.89), 7.929 (0.93), 7.941 (0.89), 7.945 (0.85), 8.741(1.59), 8.745 (1.59), 9.640 (0.44).

Example 5314-[3-({6-[4-(2-hydroxy-2-methylpropyl)-3,5-dimethyl-1H-pyrazol-1-yl]pyrimidin-4-yl}amino)-4-methoxy-1-methyl-1H-pyrazol-5-yl]benzonitrile

A solution of ethyl[1-(6-{[5-(4-cyanophenyl)-4-methoxy-1-methyl-1H-pyrazol-3-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]acetate(177 mg, 364 μmol) in tetrahydrofuran (14 ml, 170 mmol) was treated withchlorido(methyl)magnesium (420 μl, 3.0 M, 1.3 mmol) at 0° C. The mixturewas left overnight at ambient temperature. The mixture was diluted withsaturated potassium sodium tartrate solution and water and extractedwith ethyl acetate (3×). The combined organics were dried over magnesiumsulfate, concentrated under reduced pressure and purified by preparativeHPLC (method 7) to yield 70.0 mg (40%) of the desired product.

LC-MS (method 10): R_(t)=1.67 min; MS (ESIpos): m/z=473 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: 1.090 (16.00), 2.166 (10.42), 2.432(4.44), 2.519 (1.24), 2.524 (0.95), 2.569 (10.76), 3.565 (15.37), 3.785(11.96), 4.237 (4.37), 7.195 (3.11), 7.197 (3.24), 7.771 (3.04), 7.792(3.70), 8.001 (3.60), 8.022 (2.97), 8.440 (2.36), 9.371 (1.94).

Example 532

N-{1-(cyclopropylmethyl)-4-methyl-3-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-5-yl}-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-amine

A microwave vial was charged4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (105mg, 430 μmol) and1-(cyclopropylmethyl)-4-methyl-3-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-5-amine(140 mg, 472 μmol) and the contents were suspended in 1,4-dioxane (2.2ml, 26 mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (11.8 mg, 12.9 μmol) and Xantphos(14.9 mg, 25.8 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (54.9 mg, 472 μmol) was added. The vial was sealed and heatedat 85° C. for 120 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with water andextracted with dichloromethane (2×). The combined organics were filteredover a column Chromabond PTS and concentrated under reduced pressure.The crude product was purified by preparative HPLC (method 4) to yieldthe desired product (80.0 mg, 36%).

LC-MS (Method 10): R_(t)=2.30 min; MS (ESIpos): m/z=505 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: −0.008 (1.17), 0.008 (1.02), 0.316(2.83), 0.327 (3.09), 0.440 (2.90), 0.460 (3.07), 1.191 (0.43), 1.203(0.77), 1.210 (0.75), 1.222 (1.17), 1.234 (0.81), 1.240 (0.78), 1.356(0.40), 2.093 (16.00), 2.292 (2.54), 2.300 (2.43), 2.322 (1.50), 2.328(1.50), 2.367 (0.67), 2.524 (3.48), 2.665 (0.85), 2.670 (1.13), 2.705(0.54), 2.710 (0.66), 3.893 (2.43), 3.909 (2.40), 6.792 (2.74), 7.684(1.53), 7.819 (3.21), 7.955 (1.45), 7.967 (2.68), 7.987 (2.94), 8.352(1.15), 8.372 (1.09), 8.502 (0.52), 9.107 (2.00), 9.621 (0.43).

Example 533N-{1-(cyclopropylmethyl)-4-methyl-3-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-5-yl}-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (84.5 mg, 405 μmol)and1-(cyclopropylmethyl)-4-methyl-3-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-5-amine(132 mg, 445 μmol) and the contents were suspended in 1,4-dioxane (2.1ml, 25 mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (11.1 mg, 12.1 μmol) and Xantphos(14.1 mg, 24.3 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (51.7 mg, 445 μmol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with water andextracted with dichloromethane (2×). The combined organics were filteredover a column Chromabond PTS and concentrated under reduced pressure.The crude product was purified by preparative HPLC (method 4) to yieldthe desired product (80.0 mg, 42%).

LC-MS (Method 10): R_(t)=2.25 min; MS (ESIpos): m/z=469 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: −0.008 (0.59), 0.008 (0.59), 0.305(0.60), 0.317 (2.52), 0.330 (2.85), 0.342 (0.85), 0.441 (2.48), 0.461(2.69), 1.206 (0.67), 1.213 (0.65), 1.225 (1.05), 1.237 (0.63), 1.244(0.63), 2.090 (16.00), 2.178 (3.82), 2.328 (0.55), 2.333 (0.40), 2.524(1.77), 2.633 (15.04), 2.666 (0.52), 2.670 (0.67), 2.675 (0.53), 3.887(2.67), 3.904 (2.62), 6.150 (3.09), 7.963 (2.57), 7.984 (2.87), 8.350(1.27), 8.370 (1.17), 8.469 (0.92), 9.106 (2.29), 9.447 (0.93).

Example 5346-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-{1-(cyclopropylmethyl)-4-methyl-3-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-5-yl}pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (95.5 mg,393 μmol) and1-(cyclopropylmethyl)-4-methyl-3-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-5-amine(128 mg, 432 μmol) and the contents were suspended in 1,4-dioxane (2.0ml, 24 mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (10.8 mg, 11.8 μmol) and Xantphos(13.6 mg, 23.6 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (50.2 mg, 432 μmol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with water andextracted with dichloromethane (2×). The combined organics were filteredover a column Chromabond PTS and concentrated under reduced pressure.The crude product was purified by preparative HPLC (method 5) to yieldthe desired product (115mg, 54%).

LC-MS (Method 10): R_(t)=2.52 min; MS (ESIpos): m/z=503 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: 0.314 (2.13), 0.327 (2.32), 0.440(2.09), 0.460 (2.26), 1.203 (0.63), 1.222 (0.89), 1.241 (0.58), 2.089(13.43), 2.218 (2.71), 2.229 (3.23), 2.266 (0.74), 2.329 (0.67), 2.651(16.00), 2.671 (2.69), 2.679 (0.96), 3.886 (2.06), 3.904 (2.09), 7.237(0.54), 7.259 (0.41), 7.278 (0.48), 7.964 (2.18), 7.985 (2.48), 8.347(1.10), 8.367 (1.02), 8.502 (0.70), 8.719 (0.47), 9.103 (2.10), 9.549(0.50).

Example 535N-{1-(cyclopropylmethyl)-4-methyl-3-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-5-yl}-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (100 mg,420 μmol) and1-(cyclopropylmethyl)-4-methyl-3-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-5-amine(137 mg, 462 μmol) and the contents were suspended in 1,4-dioxane (2.2ml, 26 mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (11.5 mg, 12.6 μmol) and Xantphos(14.6 mg, 25.2 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (53.7 mg, 462 μmol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with water andextracted with dichloromethane (2×). The combined organics were filteredover a column Chromabond PTS and concentrated under reduced pressure.The crude product was purified by preparative HPLC (method 4) to yieldthe desired product (92.0 mg, 44%).

LC-MS (Method 10): R_(t)=2.24 min; MS (ESIpos): m/z=499 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: 0.008 (0.47), 0.314 (2.40), 0.325(2.70), 0.438 (2.40), 0.458 (2.60), 1.202 (0.66), 1.209 (0.63), 1.220(0.98), 1.238 (0.63), 2.086 (16.00), 2.187 (3.69), 2.329 (0.52), 2.524(1.60), 2.671 (0.56), 3.702 (14.04), 3.883 (2.51), 3.901 (2.45), 7.963(2.55), 7.984 (2.81), 8.346 (1.28), 8.367 (1.17), 8.454 (1.03), 9.105(2.42), 9.435 (0.89).

Example 536N-{3-[4-(difluoromethyl)phenyl]-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-yl}-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (67.4 mg, 323 μmol)and3-[4-(difluoromethyl)phenyl]-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-amine(100 mg, 355 μmol) and the contents were suspended in 1,4-dioxane (1.8ml, 22 mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (8.88 mg, 9.69 μmol) and Xantphos(11.2 mg, 19.4 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (41.3 mg, 355 μmol) was added. The vial was sealed and heatedat 85° C. for 60 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with water andextracted with dichloromethane (2×). The combined organics were driedover sodium sulfate and concentrated under reduced pressure. The crudeproduct was purified by preparative HPLC (Method 3) to yield the desiredproduct (66.7 mg, 46%).

LC-MS (Method 10): R_(t)=2.15 min; MS (ESIpos): m/z=454 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: −0.008 (0.40), 2.044 (16.00), 2.168(3.74), 2.188 (1.35), 2.328 (0.50), 2.524 (1.34), 2.630 (14.36), 2.653(0.65), 2.670 (0.54), 2.675 (0.58), 3.153 (8.78), 3.171 (0.64), 3.660(2.03), 3.674 (4.36), 3.688 (2.26), 4.136 (1.63), 6.141 (3.03), 6.937(1.44), 7.077 (3.02), 7.217 (1.26), 7.636 (2.88), 7.656 (3.51), 7.844(2.99), 7.863 (2.50), 8.471 (1.23), 9.339 (2.78).

Example 5376-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-{3-[4-(difluoromethyl)phenyl]-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-yl}pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (78.6 mg,323 μmol) and3-[4-(difluoromethyl)phenyl]-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-amine(100 mg, 355 μmol) and the contents were suspended in 1,4-dioxane (1.7ml, 20 mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (8.88 mg, 9.69 μmol) and Xantphos(11.2 mg, 19.4 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (41.3 mg, 355 μmol) was added. The vial was sealed and heatedat 85° C. for 90 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with water andextracted with dichloromethane (2×). The combined organics were driedover sodium sulfate and concentrated under reduced pressure. The crudeproduct was purified by preparative HPLC (Method 4) to yield the desiredproduct (101 mg, 64%).

LC-MS (Method 10): R_(t)=2.44 min; MS (ESIpos): m/z=488 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: 1.074 (0.64), 1.091 (1.30), 1.109(0.65), 2.043 (14.92), 2.207 (2.62), 2.524 (0.62), 2.648 (16.00), 3.146(4.92), 3.168 (0.58), 3.375 (0.65), 3.392 (0.63), 3.658 (1.76), 3.672(3.72), 3.685 (1.95), 4.139 (1.36), 6.938 (1.28), 7.078 (2.66), 7.218(1.15), 7.636 (2.55), 7.657 (3.21), 7.843 (2.52), 7.863 (2.16), 8.507(0.71), 9.443 (1.50).

Example 5386-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]-N-{3-[4-(difluoromethyl)phenyl]-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-yl}pyrimidin-4-amine

A microwave vial was charged4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (85.9mg, 351 μmol) and3-[4-(difluoromethyl)phenyl]-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-amine(150 mg, 72% purity, 386 μmol) and the contents were suspended in1,4-dioxane (1.8 ml, 21 mmol). The reaction mixture was degassed with Arfor 3 min. Tris(dibenzylidenaceton)dipalladium (9.64 mg, 10.5 μmol) andXantphos (12.2 mg, 21.1 μmol) were added and the reaction mixture wasdegassed again for 1 min and heated to 85° C. At this temperature andsodium phenolate (44.8 mg, 386 μmol) was added. The vial was sealed andheated at 85° C. for 90 minutes while vigorously stirring. As theconversion was not completed the mixture was again treated with (9.64mg, 10.5 μmol) and (12.2 mg, 21.1 μmol) and stirred for 2 hours at 85°C. After cooling to ambient temperature 20 mg of sodium phenolate wereadded (0.17 mmol) and the mixture was stirred further for 2 hours at 85°C. The mixture was purified by preparative HPLC (method: column:Reprosil C18; 10 μm; 125×30 mm/flow: 50 ml/min/eluent: A=H₂O (0.01%HCOOH), B=acetonitrile/grradient: 0.00-5.00 min=10% B, 6.50 min=20% B,17.0-19.75 min=100% B, 19.75-23.00 min=90% B) and subsequentflash-chromatography (column: SNAP KP-Sil 10 g, solvent:dichloromethane/ethyl acetate 88/12 to 100% ethyl acetate) to yield 30.2mg (17%) of the desired product.

LC-MS (Method 10): R_(t)=2.22 min; MS (ESIpos): m/z=490 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: −0.008 (1.22), 0.008 (1.02), 1.988(0.53), 2.047 (16.00), 2.278 (2.04), 2.328 (0.45), 3.139 (3.27), 3.182(0.43), 3.568 (0.65), 3.657 (1.92), 3.671 (3.86), 3.685 (2.05), 4.143(1.34), 6.781 (2.22), 6.939 (1.44), 7.079 (2.97), 7.219 (1.31), 7.639(2.83), 7.659 (3.49), 7.687 (1.42), 7.823 (2.93), 7.848 (2.16), 7.868(1.85), 7.959 (1.25), 8.503 (0.57), 9.525 (1.16).

Example 539N-{3-[4-(difluoromethyl)phenyl]-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-yl}-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (77.1 mg,323 μmol) and3-[4-(difluoromethyl)phenyl]-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-amine(100 mg, 355 μmol) and the contents were suspended in 1,4-dioxane (1.7ml, 20 mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (8.88 mg, 9.69 μmol) and Xantphos(11.2 mg, 19.4 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (41.3 mg, 355 μmol) was added. The vial was sealed and heatedat 85° C. for 120 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with water andextracted with dichloromethane (2×). The combined organics were driedover sodium sulfate and concentrated under reduced pressure. The crudeproduct was purified by preparative HPLC (method 3) and subsequent byflash-chromatography (column: SNAP KP-Sil 10 g, solvent:dichloromethane/ethyl acetate 88/12 to 100% ethyl acetate) to yield thedesired product (55.75 mg, 36%).

LC-MS (Method 10): R_(t)=2.11 min; MS (ESIpos): m/z=484 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: −0.008 (0.51), 0.008 (0.48), 1.525(0.68), 2.038 (16.00), 2.177 (3.56), 2.328 (0.59), 2.523 (1.69), 2.670(0.61), 3.151 (9.11), 3.171 (0.53), 3.656 (2.05), 3.670 (4.37), 3.684(2.60), 3.697 (13.32), 4.134 (1.63), 6.936 (1.39), 7.076 (2.91), 7.217(1.22), 7.635 (2.91), 7.655 (3.50), 7.841 (3.05), 7.861 (2.49), 8.452(1.15), 9.325 (2.70).

Example 5404-(3-{[6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-4-methoxy-1-methyl-1H-pyrazol-5-yl)benzonitrile

A microwave vial was charged4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (96.8 mg,398 μmol) and 4-(3-amino-4-methoxy-1-methyl-1H-pyrazol-5-yObenzonitrile(100 mg, 438 μmol) and the contents were suspended in 1,4-dioxane (6.0ml, 70 mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (10.9 mg, 11.9 _(t)tmol) andXantphos (13.8 mg, 23.9 μmol) were added and the reaction mixture wasdegassed again for 1 min and heated to 85° C. At this temperature andsodium phenolate (50.9 mg, 438 _(t)tmol) was added. The vial was sealedand heated at 85° C. for 90 minutes while vigorously stirring. Aftercooling to ambient temperature, the reaction mixture was diluted withwater and extracted with dichloromethane (2×). The combined organicswere filtered over a column Chromabond PTS and concentrated underreduced pressure. The crude product was purified by preparative HPLC(method 3) to yield the desired product (90.0 mg, 49%).

LC-MS (Method 10): R_(t)=2.14 min; MS (ESIpos): m/z=435 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: 2.074 (0.97), 2.215 (11.60), 2.328(0.53), 2.642 (12.80), 2.670 (0.55), 3.560 (16.00), 3.785 (12.67), 7.226(3.39), 7.341 (0.53), 7.382 (0.66), 7.461 (0.93), 7.465 (0.93), 7.478(0.56), 7.772 (3.27), 7.793 (4.37), 7.814 (0.48), 7.820 (0.50), 8.004(3.92), 8.025 (3.22), 8.490 (3.00), 9.550 (1.37).

Example 5414-[3-({6-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidin-4-yl}amino)-4-methoxy-1-methyl-1H-pyrazol-5-yl]benzonitrile

A microwave vial was charged4-chloro-6-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidine(110 mg, 398 μmol) and4-(3-amino-4-methoxy-1-methyl-1H-pyrazol-5-yl)benzonitrile (100 mg, 438μmol) and the contents were suspended in 1,4-dioxane (6.0 ml, 70 mmol).The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (10.9 mg, 11.9 μmol) and Xantphos(13.8 mg, 23.9 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (50.9 mg, 438 μmol) was added. The vial was sealed and heatedat 85° C. for 120 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with water andextracted with dichloromethane (2×). The combined organics were filteredover a column Chromabond PTS and concentrated under reduced pressure.The crude product was purified by preparative HPLC (method 3) to yieldthe desired product (45.0 mg, 24%).

LC-MS (Method 10): R_(t)=2.15 min; MS (ESIpos): m/z=469 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: 2.074 (1.99), 2.304 (6.31), 2.328(0.51), 2.671 (0.40), 2.744 (6.56), 3.564 (16.00), 3.782 (13.19), 7.251(3.38), 7.772 (3.38), 7.793 (4.07), 8.005 (4.00), 8.026 (3.27), 8.544(2.94), 9.686 (0.91).

Example 5426-(3,5-dimethyl-1H-pyrazol-1-yl)-N-[3-(5-fluoropyridin-2-yl)-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-yl]pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (79.6 mg, 381 μmol)and3-(5-fluoropyridin-2-yl)-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-amine(105 mg, 420 μmol) and the contents were suspended in 1,4-dioxane (2.5ml, 29 mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (10.5 mg, 11.4 μmol) and Xantphos(13.2 mg, 22.9 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (48.7 mg, 420 μmol) was added. The vial was sealed and heatedat 85° C. for 60 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with water andextracted with dichloromethane (2×). The combined organics were driedover sodium sulfate and concentrated under reduced pressure. The crudeproduct was purified by preparative HPLC (method 3) to yield the desiredproduct (48.6 mg, 29%).

LC-MS (Methdo 10): R_(t)=2.01 min; MS (ESIpos): m/z=423 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: −0.008 (0.49), 0.008 (0.43), 2.142(16.00), 2.156 (2.93), 2.228 (1.41), 2.328 (0.41), 2.524 (1.12), 2.626(13.06), 2.664 (1.25), 2.670 (0.46), 3.146 (5.91), 3.659 (1.79), 3.673(3.75), 3.686 (1.94), 4.147 (1.33), 6.135 (2.31), 7.752 (0.61), 7.759(0.65), 7.774 (1.32), 7.781 (1.39), 7.796 (0.75), 7.803 (0.77), 7.982(0.94), 7.994 (1.00), 8.004 (0.85), 8.016 (0.77), 8.464 (0.70), 8.594(2.23), 8.601 (2.22), 9.333 (2.75).

Example 5436-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]-N-[3-(5-fluoropyridin-2-yl)-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-yl]pyrimidin-4-amine

A microwave vial was charged4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (93.3mg, 381 μmol) and3-(5-fluoropyridin-2-yl)-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-amine(105 mg, 420 μmol) and the contents were suspended in 1,4-dioxane (2.5ml, 29 mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (10.5 mg, 11.4 μmol) and Xantphos(13.2 mg, 22.9 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (48.7 mg, 420 μmol) was added. The vial was sealed and heatedat 85° C. for 60 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with water andextracted with dichloromethane (2×). The combined organics were filteredover a column Chromabond PTS and concentrated under reduced pressure.The crude product was purified by preparative HPLC (method 3) to yieldthe desired product (32.1 mg, 18%).

LC-MS (Method 10): R_(t)=2.12 min; MS (ESIpos): m/z=459 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: −0.008 (0.85), 0.008 (0.66), 2.145(16.00), 2.266 (1.41), 2.323 (0.67), 2.328 (0.82), 2.332 (0.65), 2.523(1.95), 2.665 (0.54), 2.670 (0.74), 2.675 (0.54), 2.697 (0.51), 3.131(2.15), 3.656 (1.57), 3.670 (3.12), 3.683 (1.69), 4.152 (1.01), 6.775(1.77), 7.683 (1.27), 7.757 (0.44), 7.764 (0.52), 7.779 (1.04), 7.787(1.13), 7.801 (0.66), 7.809 (0.68), 7.819 (2.62), 7.955 (1.15), 7.987(0.66), 7.999 (0.75), 8.009 (0.70), 8.599 (1.99), 8.606 (2.02), 9.524(1.07).

Example 544N-[3-(5-fluoropyridin-2-yl)-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-yl]-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (91.0 mg,381 μmol) and3-(5-fluoropyridin-2-yl)-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-amine(105 mg, 420 μmol) and the contents were suspended in 1,4-dioxane (2.5ml, 29 mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (10.5 mg, 11.4 μmol) and Xantphos(13.2 mg, 22.9 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (48.7 mg, 420 μmol) was added. The vial was sealed and heatedat 85° C. for 120 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with water andextracted with dichloromethane (2×). The combined organics were driedover sodium sulfate and concentrated under reduced pressure. The crudeproduct was purified by preparative HPLC (method 3) and subsequentflash-chromatography (column: SNAP KP_Sil 10 g, solvent:dichloromethane/ethyl acetate 88/12 to 0/100) to yield the desiredproduct (70.0 mg, 41%).

LC-MS (Method 10): R_(t)=1.96 min; MS (ESIpos): m/z=453 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: −0.008 (0.48), 2.041 (0.40), 2.137(16.00), 2.166 (2.74), 2.328 (0.48), 2.524 (1.29), 2.671 (0.45), 3.145(6.73), 3.655 (1.80), 3.670 (3.83), 3.693 (11.51), 4.143 (1.33), 7.751(0.61), 7.759 (0.66), 7.774 (1.36), 7.781 (1.44), 7.796 (0.79), 7.803(0.77), 7.981 (0.99), 7.993 (1.07), 8.004 (0.91), 8.015 (0.82), 8.448(0.88), 8.594 (2.54), 8.601 (2.51), 9.320 (2.68).

Example 545 ethyl1-(6-{[3-(5-fluoropyridin-2-yl)-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate

A microwave vial was charged ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (107mg, 381 μmol) and 3-(5-fluoropyridin-2-yl)-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-amine (105 mg, 420 μmol) and the contentswere suspended in 1,4-dioxane (2.5 ml, 29 mmol). The reaction mixturewas degassed with Ar for 3 min. Tris(dibenzylidenaceton)dipalladium(10.5 mg, 11.4 μmol) and Xantphos (13.2 mg, 22.9 μmol) were added andthe reaction mixture was degassed again for 1 min and heated to 85° C.At this temperature and sodium phenolate (48.7 mg, 420 μmol) was added.The vial was sealed and heated at 85° C. for 60 minutes while vigorouslystirring. After cooling to ambient temperature, the reaction mixture wasdiluted with water and extracted with dichloromethane (2×). The combinedorganics were dried over sodium sulfate and concentrated under reducedpressure. The crude product was purified by preparative HPLC (method 3)to yield the desired product (82.5 mg, 44%).

LC-MS (Method 10): R_(t)=2.18 min; MS (ESIpos): m/z=495 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: 1.283 (2.98), 1.301 (6.03), 1.319(3.03), 2.145 (16.00), 2.358 (1.75), 2.524 (1.24), 2.671 (0.44), 2.904(12.52), 3.143 (3.24), 3.659 (1.66), 3.672 (3.33), 3.686 (1.77), 4.146(1.24), 4.224 (0.97), 4.241 (2.70), 4.259 (2.66), 4.277 (0.92), 7.751(0.58), 7.758 (0.66), 7.773 (1.29), 7.781 (1.38), 7.795 (0.76), 7.803(0.74), 7.980 (0.95), 7.991 (1.03), 8.001 (0.91), 8.013 (0.80), 8.538(0.54), 8.593 (2.56), 8.600 (2.57), 9.512 (1.17).

Example 546 ethyl1-[6-({3-[4-(difluoromethyl)phenyl]-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3,5-dimethyl-1H-pyrazole-4-carboxylate

A microwave vial was charged ethyl1-(6-chloropyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylate (227mg, 808 μmol) and3-[4-(difluoromethyl)phenyl]-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-amine(250 mg, 889 μmol) and the contents were suspended in 1,4-dioxane (4.6ml, 54 mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (22.2 mg, 24.2 μmol) and Xantphos(28.0 mg, 48.5 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (103 mg, 889 μmol) was added. The vial was sealed and heatedat 85° C. for 60 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with water andextracted with dichloromethane (2×). The combined organics were driedover sodium sulfate and concentrated under reduced pressure. The crudeproduct was purified by preparative HPLC (method 4) to yield the desiredproduct (153 mg, 34%).

LC-MS (Method 10): R_(t)=2.29 min; MS (ESIpos): m/z=526 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: −0.008 (0.46), 1.287 (3.51), 1.304(7.18), 1.322 (3.57), 2.046 (16.00), 2.329 (0.74), 2.333 (0.68), 2.368(2.55), 2.524 (1.47), 2.671 (0.51), 2.908 (13.13), 3.148 (4.42), 3.651(2.04), 3.659 (2.02), 3.673 (3.92), 3.687 (2.07), 4.143 (1.45), 4.228(1.11), 4.245 (3.20), 4.263 (3.17), 4.281 (1.05), 6.938 (1.40), 7.077(3.07), 7.217 (1.30), 7.342 (1.44), 7.382 (1.62), 7.461 (2.27), 7.465(2.43), 7.478 (1.44), 7.636 (2.97), 7.656 (3.64), 7.781 (1.39), 7.790(1.12), 7.794 (1.31), 7.807 (0.98), 7.814 (1.16), 7.821 (1.33), 7.841(2.92), 7.861 (2.49), 8.548 (0.72), 9.518 (1.09).

Example 5474-[5-({6-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidin-4-yl}amino)-1,4-dimethyl-1H-pyrazol-3-yl]benzonitrile

A microwave vial was charged with4-chloro-6-[3,5-dimethyl-4-(trifluoromethyl)-1H-pyrazol-1-yl]pyrimidine(112 mg, 95% purity, 385 μmol) and4-(5-amino-1,4-dimethyl-1H-pyrazol-3-yl)benzonitrile (100 mg, 90%purity, 424 μmol) and the contents were suspended in dioxane (1.2 mL).The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylideneacetone)dipalladium (7.06 mg, 7.71 μmol) and XantPhos(8.92 mg, 15.4 μmol) were added and the reaction mixture was degassedagain for 1 min. Lastly, sodium phenolate (49.2 mg, 424 μmol) was added,the vial was sealed and heated at 85° C. overnight while vigorouslyshaking. After cooling to ambient temperature, the reaction mixture wasdiluted with dimethylsulfoxide and the precipitated solid was collectedby filtration. The solid was redissolved in dichloromethane and purifiedby flash column chromatography (SNAP Ultra 10 g, cyclohexane/EtOAcgradient) to yield the desired product (16 mg, 9% yield).

LC-MS (method 11): R_(t)=1.51 min; MS (ESIpos): m/z=453 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: −0.008 (1.01), 0.008 (1.04), 1.235(1.57), 1.489 (0.41), 2.076 (13.10), 2.193 (0.92), 2.285 (1.24), 2.309(2.21), 2.759 (6.27), 3.702 (7.50), 7.896 (16.00), 8.554 (0.49), 9.670(0.77).

Example 5486-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]-N-{1,4-dimethyl-3-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-5-yl}pyrimidin-4-amine

A microwave vial was charged4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (108mg, 443 μmol) and1,4-dimethyl-3-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-5-amine (125mg, 488 μmol) and the contents were suspended in 1,4-dioxane (2.3 ml, 27mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (12.2 mg, 13.3 μmol) and Xantphos(15.4 mg, 26.6 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (56.6 mg, 488 μmol) was added. The vial was sealed and heatedat 85° C. for 120 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with water andextracted with DCM (2×). The combined organics were filtered over acolumn Chromabond PTS and concentrated under reduced pressure. The crudeproduct was purified by preparative HPLC (method 4) to yield the desiredproduct (83.0 mg, 36%).

LC-MS (Method 10): R_(t)=2.15 min; MS (ESIpos): m/z=465 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: −0.008 (0.64), 0.008 (0.57), 1.091(0.54), 1.647 (0.82), 2.104 (16.00), 2.295 (2.73), 3.727 (8.48), 6.796(2.66), 7.369 (0.64), 7.385 (0.60), 7.399 (0.76), 7.685 (1.20), 7.821(2.45), 7.959 (2.68), 7.980 (2.34), 8.337 (1.02), 8.358 (0.94), 8.512(0.61), 9.097 (1.76), 9.673 (1.14).

Example 5496-(3,5-dimethyl-1H-pyrazol-1-yl)-N-{1,4-dimethyl-3-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-5-yl}pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (94.0 mg, 451 μmol)and 1,4-dimethyl-3-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-5-amine(127 mg, 496 μmol) and the contents were suspended in 1,4-dioxane (2.3ml, 27 mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (12.4 mg, 13.5 μmol) and Xantphos(15.6 mg, 27.0 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (57.5 mg, 496 μmol) was added. The vial was sealed and heatedat 85° C. for 120 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with water andextracted with DCM (2×). The combined organics were filtered over acolumn Chromabond PTS and concentrated under reduced pressure. The crudeproduct was purified by preparative HPLC (method 3) to yield the desiredproduct (90.0 mg, 47%).

LC-MS (Method 10): R_(t)=2.06 min; MS (ESIpos): m/z=429 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: −0.008 (0.71), 0.008 (0.69), 1.074(0.73), 1.091 (1.48), 1.109 (0.74), 2.101 (16.00), 2.183 (4.74), 2.635(13.30), 3.375 (0.75), 3.392 (0.74), 3.720 (12.00), 6.154 (2.94), 7.957(2.23), 7.978 (2.51), 8.332 (1.18), 8.353 (1.08), 8.479 (1.08), 9.096(1.96), 9.491 (2.40).

Example 5506-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-{1,4-dimethyl-3-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-5-yl}pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (110 mg,454 μmol) and1,4-dimethyl-3-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-5-amine (128mg, 500 μmol) and the contents were suspended in 1,4-dioxane (2.4 ml, 28mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (12.5 mg, 13.6 μmol) and Xantphos(15.8 mg, 27.2 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (58.0 mg, 500 μmol) was added. The vial was sealed and heatedat 85° C. for 120 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with water andextracted with DCM (2×). The combined organics were filtered over acolumn Chromabond PTS and concentrated under reduced pressure. The crudeproduct was purified by preparative HPLC (method 4) to yield the desiredproduct (90.0 mg, 43%).

LC-MS (Method 10): R_(t)=2.36 min; MS (ESIpos): m/z=463 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: −0.008 (0.68), 0.008 (0.65), 1.074(1.20), 1.091 (2.45), 1.109 (1.23), 2.086 (2.01), 2.099 (15.27), 2.222(3.70), 2.265 (0.77), 2.652 (16.00), 2.678 (0.78), 3.357 (0.44), 3.375(1.22), 3.392 (1.19), 3.721 (10.57), 7.957 (2.14), 7.978 (2.37), 8.331(1.10), 8.354 (1.01), 8.515 (0.97), 9.094 (2.06), 9.593 (1.41).

Example 551N-{1,4-dimethyl-3-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-5-yl}-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(4-methoxy-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (108 mg,454 μmol) and1,4-dimethyl-3-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-5-amine (128mg, 500 μmol) and the contents were suspended in 1,4-dioxane (2.4 ml, 28mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (12.5 mg, 13.6 μmol) and Xantphos(15.8 mg, 27.2 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (58.0 mg, 500 μmol) was added. The vial was sealed and heatedat 85° C. for 120 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with water andextracted with DCM (2×). The combined organics were filtered over acolumn Chromabond PTS and concentrated under reduced pressure. The crudeproduct was purified by preparative HPLC (method 3) to yield the desiredproduct (128.0 mg, 61%).

LC-MS (Method 10): R_(t)=2.06 min; MS (ESIpos): m/z=459 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: −0.008 (0.62), 0.008 (0.57), 1.074(0.62), 1.091 (1.28), 1.109 (0.64), 2.096 (16.00), 2.193 (4.52), 3.375(0.64), 3.392 (0.63), 3.706 (15.37), 3.716 (12.45), 7.957 (2.16), 7.978(2.44), 8.331 (1.17), 8.335 (1.15), 8.351 (1.06), 8.462 (1.05), 9.091(1.92), 9.478 (2.36).

Example 5526-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]-N-{1,4-dimethyl-5-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-3-yl}pyrimidin-4-amine

A microwave vial was charged4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (104mg, 426 μmol) and1,4-dimethyl-5-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-3-amine (120mg, 468 μmol) and the contents were suspended in 1,4-dioxane (2.5 ml, 29mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (11.7 mg, 12.8 μmol) and Xantphos(14.8 mg, 25.5 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (54.4 mg, 468 μmol) was added. The vial was sealed and heatedat 85° C. for 120 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with water andextracted with DCM (2×). The combined organics were filtered over acolumn Chromabond PTS and concentrated under reduced pressure. The crudeproduct was purified by preparative HPLC (method 3) to yield the desiredproduct (45.0 mg, 23%).

LC-MS (Method 10): R_(t)=2.13 min; MS (ESIpos): m/z=465 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: 1.921 (11.83), 2.300 (13.63), 3.775(0.75), 3.787 (16.00), 6.777 (3.73), 7.462 (0.88), 7.694 (1.18), 7.830(2.44), 7.966 (1.05), 8.078 (2.14), 8.098 (2.63), 8.262 (1.47), 8.267(1.40), 8.283 (1.19), 8.287 (1.15), 8.491 (2.74), 8.929 (2.27), 8.934(2.19), 9.680 (1.90).

Example 5536-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)-N-{1,4-dimethyl-5-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-3-yl}pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(4-chloro-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (103 mg,426 μmol) and1,4-dimethyl-5-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-3-amine (120mg, 468 μmol) and the contents were suspended in 1,4-dioxane (2.5 ml, 29mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (11.7 mg, 12.8 μmol) and Xantphos(14.8 mg, 25.5 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (54.4 mg, 468 μmol) was added. The vial was sealed and heatedat 85° C. for 120 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with water andextracted with DCM (2×). The combined organics were filtered over acolumn Chromabond PTS and concentrated under reduced pressure. The crudeproduct was purified by preparative HPLC (method 4) to yield the desiredproduct (45.0 mg, 23%).

LC-MS (Method 10): R_(t)=2.32 min; MS (ESIpos): m/z=463 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: 0.008 (0.48), 1.917 (13.01), 2.227(14.26), 2.645 (15.36), 3.776 (16.00), 7.433 (1.18), 8.074 (2.10), 8.095(2.54), 8.256 (1.52), 8.260 (1.44), 8.276 (1.19), 8.280 (1.14), 8.496(2.78), 8.923 (2.28), 9.592 (2.31).

Example 5544-[5-({6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidin-4-yl}amino)-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile

A microwave vial was charged4-chloro-6-[5-(difluoromethyl)-3-methyl-1H-pyrazol-1-yl]pyrimidine (104mg, 426 μmol) and4-[5-amino-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile (120mg, 468 μmol) and the contents were suspended in 1,4-dioxane (2.5 ml, 29mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (11.7 mg, 12.8 μmol) and Xantphos(14.8 mg, 25.5 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (54.4 mg, 468 μmol) was added. The vial was sealed and heatedat 85° C. for 120 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with water andextracted with DCM (2×). The combined organics were filtered over acolumn Chromabond PTS and concentrated under reduced pressure. The crudeproduct was purified by preparative HPLC (method 3) to yield the desiredproduct (55.0 mg, 27%).

LC-MS (Method 10): R_(t)=2.12 min; MS (ESIpos): m/z=465 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: −0.008 (1.66), 0.008 (1.01), 2.061(16.00), 2.284 (2.35), 2.699 (0.46), 3.138 (3.50), 3.177 (0.72), 3.660(1.89), 3.674 (3.65), 3.687 (1.95), 4.154 (1.33), 6.783 (2.35), 7.684(1.33), 7.819 (2.70), 7.911 (10.45), 7.956 (1.33), 8.500 (0.74), 9.552(1.20).

Example 5554-[5-{[6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl]amino}-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (88.8 mg, 426 μmol)and 4-[5-amino-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-3-yl]benzonitrile(120 mg, 468 μmol) and the contents were suspended in 1,4-dioxane (2.5ml, 29 mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (11.7 mg, 12.8 μmol) and Xantphos(14.8 mg, 25.5 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (54.4 mg, 468 μmol) was added. The vial was sealed and heatedat 85° C. for 120 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with water andextracted with DCM (2×). The combined organics were filtered over acolumn Chromabond PTS and concentrated under reduced pressure. The crudeproduct was purified by preparative HPLC (method 2) to yield the desiredproduct (94.0 mg, 49%).

LC-MS (Method 10): R_(t)=2.03 min; MS (ESIpos): m/z=429 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: −0.008 (0.79), 0.008 (0.71), 1.646(0.74), 2.059 (16.00), 2.169 (3.65), 2.628 (13.61), 3.150 (8.75), 3.663(1.95), 3.677 (4.13), 3.691 (2.14), 4.147 (1.58), 6.143 (2.93), 7.369(0.53), 7.385 (0.52), 7.398 (0.65), 7.885 (0.71), 7.907 (13.16), 7.932(0.63), 8.466 (1.11), 9.367 (2.73).

Example 556 methyl[1-(6-{[1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazol-4-yl]carbamate

A solution of tert-butyl[6-(4-amino-3,5-dimethyl-1H-pyrazol-1-yl)pyrimidin-4-yl][1-(cyclopropylmethyl)-3-(4-fluorophenyl)-4-methyl-1H-pyrazol-5-yl]carbamate(125 mg, 235 μmol) and methyl carbonochloridate (33.3 mg, 352 μmol) indichloromethane (2.5 mL) was treated with triethylamine (65 μl, 470μmol) and stirred for 3 hours at ambient temperature. The mixture wasdiluted with dichloromethane. The organic phase was dried overChromabond PTS and concentrated under reduced pressure. The residue wasresolved in 4M hydrochloric acid in dioxane and stirred for 30 min atambient temperature. The mixture was concentrated under reduced pressureand the crude product was purified by preparative HPLC (method 3) toyield 36.1 mg (31%) of the desired product.

LC-MS (Method 10): R_(t)=1.91 min; MS (ESIpos): m/z=491 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: −0.008 (0.43), 0.291 (2.21), 0.304(2.41), 0.422 (2.29), 0.442 (2.44), 1.073 (1.12), 1.091 (2.32), 1.109(1.16), 1.175 (0.62), 1.182 (0.60), 1.194 (0.95), 1.206 (0.57), 1.213(0.58), 2.009 (14.04), 2.075 (2.58), 2.488 (16.00), 3.357 (0.40), 3.375(1.15), 3.392 (1.11), 3.631 (3.56), 3.829 (2.05), 3.846 (2.01), 7.251(2.19), 7.274 (4.44), 7.296 (2.36), 7.717 (1.37), 7.731 (1.81), 7.751(1.26), 8.468 (0.63), 8.694 (0.76), 9.394 (0.55).

Example 5571-(6-{[3-(5-fluoropyridin-2-yl)-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-N,N,3,5-tetramethyl-1H-pyrazole-4-carboxamide

A solution of1-(6-{[3-(5-fluoropyridin-2-yl)-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-yl]amino}pyrimidin-4-yl)-3,5-dimethyl-1H-pyrazole-4-carboxylicacid (26.6 mg, 57.0 μmol) and N-methylmethanamine (57 μl, 2.0 M intetrahydrofuran, 110 μmol) in dimethylformamide (1.0 ml, 13 mmol) wastreated with N,N-diisopropylethylamine (30 μl, 170 μmol) and(1-[Bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium3-oxid hexafluorophosphate) (32.5 mg, 85.5 μmol) and the mixture wasstirred 30 min at ambient temperature. The mixture was diluted withwater and extracted with DCM. The organic phase was filtered overChromabond PTS concentrated under reduced pressure. The crude productwas purified by preparative HPLC (method 7) to yield 19.3 mg (68%) ofthe desired product.

LC-MS (Method 10): R_(t)=1.56 min; MS (ESIpos): m/z=494 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: −0.008 (0.50), 1.073 (0.55), 1.091(1.10), 1.109 (0.55), 2.146 (16.00), 2.583 (15.20), 2.902 (2.60), 2.975(2.87), 3.148 (4.51), 3.375 (0.55), 3.392 (0.55), 3.661 (1.62), 3.675(3.35), 3.688 (1.76), 4.151 (1.10), 7.754 (0.54), 7.761 (0.60), 7.776(1.20), 7.783 (1.30), 7.798 (0.71), 7.805 (0.74), 7.984 (0.81), 7.995(0.86), 8.006 (0.76), 8.017 (0.69), 8.500 (0.52), 8.595 (2.23), 8.602(2.24), 9.416 (1.72).

Example 5581-[6-({3-[4-(difluoromethyl)phenyl]-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-N,N,3,5-tetramethyl-1H-pyrazole-4-carboxamide

A solution of1-[6-({3-[4-(difluoromethyl)phenyl]-1-(2-methoxyethyl)-4-methyl-1H-pyrazol-5-yl}amino)pyrimidin-4-yl]-3,5-dimethyl-1H-pyrazole-4-carboxylicacid (57.7 mg, 116 μmol) and N-methylmethanamine (120 μl, 2.0 M, 230μmol) in dimethylformamide (1.0 ml, 13 mmol) was treated withN,N-diisopropylethylamine (61 μl, 350 μmol) and(1-[Bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium3-oxid hexafluorophosphate) (66.1 mg, 174 μmol) and the mixture wasstirred overnight at ambient temperature. The mixture was diluted withwater and extracted with DCM. The combined organics were washed the withbrine, dried over sodium sulfate and concentrated under reducedpressure. The crude product was purified by preparative HPLC (method 7)to yield 41.0 mg (67%) of the desired product.

LC-MS (Method 10): R_(t)=1.75 min; MS (ESIpos): m/z=525 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: −0.008 (0.55), 0.008 (0.42), 1.074(0.58), 1.091 (1.19), 1.109 (0.60), 2.047 (14.98), 2.149 (2.50), 2.586(16.00), 2.907 (2.88), 2.977 (3.11), 3.155 (6.39), 3.375 (0.60), 3.392(0.58), 3.662 (1.87), 3.676 (3.98), 3.690 (2.07), 4.142 (1.36), 6.938(1.35), 7.078 (2.85), 7.218 (1.21), 7.636 (2.62), 7.657 (3.25), 7.844(2.54), 7.864 (2.13), 8.505 (0.69), 9.421 (1.68).

Example 5596-(3,5-dimethyl-1H-pyrazol-1-yl)-N-{1,4-dimethyl-5-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-3-yl}pyrimidin-4-amine

A microwave vial was charged4-chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyrimidine (88.8 mg, 426 μmol)and 1,4-dimethyl-5-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrazol-3-amine(120 mg, 468 μmol) and the contents were suspended in 1,4-dioxane (2.5ml, 29 mmol). The reaction mixture was degassed with Ar for 3 min.Tris(dibenzylidenaceton)dipalladium (11.7 mg, 12.8 μmol) and Xantphos(14.8 mg, 25.5 μmol) were added and the reaction mixture was degassedagain for 1 min and heated to 85° C. At this temperature and sodiumphenolate (54.4 mg, 468 μmol) was added. The vial was sealed and heatedat 85° C. for 120 minutes while vigorously stirring. After cooling toambient temperature, the reaction mixture was diluted with water andextracted with DCM (2×). The combined organics were filtered over acolumn Chromabond PTS and concentrated under reduced pressure. The crudeproduct was purified by preparative HPLC (method 7) and subsequently byflash-chromatography on silica gel (column: Kp Sil 10 g, solvent:dichloromethane/ethyl acetate 1:1). The pure product was resolved in DCMand dried to yield the desired product (56.0 mg, 31%).

LC-MS (Method 10): R_(t)=1.98 min; MS (ESIpos): m/z=429 [M+H]⁺

¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: 1.915 (13.61), 2.189 (14.40), 2.626(12.12), 3.776 (16.00), 5.754 (0.95), 6.137 (3.54), 7.403 (1.84), 8.074(2.01), 8.094 (2.46), 8.256 (1.36), 8.260 (1.34), 8.276 (1.07), 8.281(1.09), 8.461 (3.43), 8.923 (2.26), 8.928 (2.24), 9.469 (2.72).

EXPERIMENTAL SECTION—BIOLOGICAL ASSAYS

Biological Investigations

The example testing experiments described herein serve to illustrate thepresent invention and the invention is not limited to the examplesgiven.

The following assays can be used to illustrate the commercial utility ofthe compounds according to the present invention.

Examples were tested in selected biological assays one or more times.When tested more than once, data are reported as either average valuesor as median values, wherein

-   -   the average value, also referred to as the arithmetic mean        value, represents the sum of the values obtained divided by the        number of times tested, and    -   the median value represents the middle number of the group of        values when ranked in ascending or descending order. If the        number of values in the data set is odd, the median is the        middle value. If the number of values in the data set is even,        the median is the arithmetic mean of the two middle values.

Examples were synthesized one or more times. When synthesized more thanonce, data from biological assays represent average values calculatedutilizing data sets obtained from testing of one or more syntheticbatch.

The in vitro activity of the compounds of the present invention can bedemonstrated in the following assays:

Biological Assays:

For measuring Npt2a activity in a cell based assay, a stable CHO cellline with inducible Npt2a expression was generated. Therefore, CHO T-Rexcells (life technologies cat. R718-07) were stably transfected withdoxycycline-inducible human NPT2a (pcDNA5TO-hNpt2a). The obtained CHOT-REx hNpt2a cells were routinely cultured in Dulbecco's MEM/F12 (4.5g/l Glucose, Gibco cat. 21331-020; 500 mL) supplemented with 10 mlGlutamax 100×, Sodium pyruvate (7 mL of 100 mM solution), HEPES (10 mLof 1 M solution), Sodium bicarbonate (10 mL of 7,5% solution), 10% FetalBovine Serum Tetracycline free (Clontech cat. 631106, 500 ml),Penicillin-Streptomycin (5 mL of 100× Solution), Blasticidin 10 μg/mLand 400 μg/mL Hy gromycin.

Activity of Npt2a was detected by following depolarization of cellularmembrane potential by influx of sodium phosphate using fluorescentmembrane potential dye kit BLUE (Molecular devices cat. R8034). ForNpt2a activity measurements, CHO T-Rex hNpt2a cells were seeded into1536 well microtiter plates (GREINER Bio-One cat. 782092) with 750cells/well in 7 μL/w of complete medium (2% Tetracycline-free FBS, 2%Poly-D-Lysine) without selective agents +Doxycycline 0.5 μg/mL to induceNpt2a gene expression, and grown for 24h at 37° C., 5% carbon dioxide.

On the day of experiment a 1× MPdye Loading Solution was freshlyprepared by re-suspending 15 mg of Blue MPdye powder in 10 mL of NHEbuffer sodium-free (140 mM N-Methyl-D-glucamine, 5.4 mM KCl, 1 mM CaCl2,11 mM D(+)-Glucose water free, 1.2 mM MgCl2, 10 mM HEPES; pH 7.4(adjusted with hydrochloric acid); sterile filtered). 5 μl medium wasremoved from plates by robotic manipulation, then 5 μL/well ofsodium-free NHE buffer was added. After incubation for 2 min, thiswashing step was repeated once. Then, 5 μL/w of buffer was removed fromplates and cells were incubated for 5 min at room temperature with 5μL/w of MPdye Loading Solution (1× in Sodium-free NHE Buffer). Testcompounds were added to the cells at final test concentrations between50 μM and 1 nM (0.6 μL/well, final DMSO 0.6%, prepared in MPDye LoadingSolution) and incubated for 5 min at room temperature.

Plates were analyzed with an in house CCD camera device using a λexc510-545 nm/λem 565-625 nm filter. Fluorescence was detected for 15 sec(background measurement M1). Activity of Npt2a was triggered by additionof 2 μL/well of 30 mM Na+ and 1 mM phosphate (prepared in a mixture ofNHE Buffer Na+ free and NHE Buffer 140 mM Na+). Fluorescence wasfollowed for 2-3 min (depolarization measurement M2). Data wasnormalized to cell number and dye loading efficiency by calculatingM2/M1. This quotient was plotted against test compound concentration.Graph Pad Prism or equivalent in house software was used to createsigmoidal dose-response curves (variable slope) and determine IC₅₀values.

TABLE 1 Assay results on activity on human Npt2a Npt2a, human Example NoIC₅₀ [nM] Example 1 4.48 Example 2 12 Example 3 13 Example 4 28.3Example 5 27.5 Example 6 49 Example 7 36 Example 8 38 Example 9 40Example 10 33.7 Example 11 50.3 Example 12 50 Example 13 61.9 Example 1470 Example 15 72 Example 16 81 Example 17 100 Example 18 110 Example 19110 Example 20 120 Example 21 140 Example 22 150 Example 23 315 Example24 310 Example 25 1070 Example 26 460 Example 27 460 Example 28 490Example 29 1420 Example 30 620 Example 31 670 Example 32 690 Example 331000 Example 34 1000 Example 35 1400 Example 36 1700 Example 37 1700Example 38 2350 Example 39 3.2 Example 40 2760 Example 41 11 Example 427.67 Example 43 144 Example 44 5.35 Example 45 29 Example 46 6.5 Example47 89 Example 48 310 Example 49 310 Example 50 160 Example 51 100Example 52 83 Example 53 11.3 Example 54 90.3 Example 55 133 Example 5620.5 Example 57 117 Example 58 760 Example 59 12 Example 60 43 Example61 4.4 Example 62 135 Example 63 7.65 Example 64 6.25 Example 65 130Example 66 87 Example 67 3.45 Example 68 31.5 Example 69 8.4 Example 7036 Example 71 50 Example 72 15.4 Example 73 15.7 Example 74 1260 Example75 42 Example 76 190 Example 77 2230 Example 78 247 Example 79 31Example 80 44 Example 81 11 Example 82 1500 Example 83 1300 Example 8475.5 Example 85 130 Example 86 50 Example 87 32 Example 88 28.5 Example89 4.8 Example 90 133 Example 91 5.73 Example 92 820 Example 93 29Example 94 2500 Example 95 63.5 Example 96 110 Example 97 75 Example 9851 Example 99 50 Example 100 360 Example 101 11.5 Example 102 7.3Example 103 64 Example 104 150 Example 105 235 Example 106 120 Example107 293 Example 108 94 Example 109 50.3 Example 110 22 Example 111 360Example 112 59.5 Example 113 32 Example 114 290 Example 115 <1.6 Example116 92.5 Example 117 19 Example 118 7.0 Example 119 870 Example 120 1450Example 121 <1.6 Example 122 25 Example 123 395 Example 124 155 Example125 20.3 Example 126 975 Example 127 1200 Example 128 1300 Example 12978 Example 130 28 Example 131 1600 Example 132 39 Example 133 57 Example134 180 Example 135 700 Example 136 360 Example 137 71 Example 138 150Example 139 130 Example 140 23 Example 141 3 Example 142 3 Example 143415 Example 144 520 Example 145 170 Example 146 126 Example 147 3Example 148 80 Example 149 7 Example 150 3 Example 151 390 Example 152 6Example 153 410 Example 154 3 Example 155 9 Example 156 2 Example 157 6Example 158 4 Example 159 8 Example 160 1110 Example 161 2 Example 16297 Example 163 71 Example 164 11 Example 165 3 Example 166 9 Example 167550 Example 168 15 Example 169 690 Example 170 440 Example 171 12Example 172 57 Example 173 16 Example 174 33 Example 175 14 Example 17613 Example 177 41 Example 178 26 Example 179 170 Example 180 47 Example181 1500 Example 182 106 Example 183 930 Example 184 1200 Example 185 27Example 186 60 Example 187 10 Example 188 710 Example 189 74 Example 190210 Example 191 3 Example 192 16 Example 193 51 Example 194 1300 Example195 3 Example 196 2 Example 197 28 Example 198 12 Example 199 36 Example200 8 Example 201 6 Example 202 13 Example 203 1400 Example 204 3Example 205 20 Example 206 9 Example 207 18 Example 208 465 Example 20918 Example 210 13 Example 211 200 Example 212 1170 Example 213 2 Example214 86 Example 215 250 Example 216 12 Example 217 2 Example 218 32Example 219 <1.6 Example 220 320 Example 221 6 Example 222 44 Example223 36 Example 224 47 Example 225 8 Example 226 190 Example 227 16Example 228 210 Example 229 350 Example 230 830 Example 231 2 Example232 6 Example 233 29 Example 234 28 Example 235 3 Example 236 3 Example237 15 Example 238 83 Example 239 290 Example 240 18 Example 241 7Example 242 21 Example 243 28 Example 244 8 Example 245 660 Example 246340 Example 247 29 Example 248 182 Example 249 22 Example 250 21 Example251 14 Example 252 48 Example 253 67 Example 254 150 Example 255 2Example 256 35 Example 257 74 Example 258 2800 Example 259 50 Example260 140 Example 261 20 Example 262 33 Example 263 111 Example 264 500Example 265 180 Example 266 410 Example 267 27 Example 268 8 Example 26953 Example 270 12 Example 271 39 Example 272 340 Example 273 120 Example274 44 Example 275 1050 Example 276 25 Example 277 150 Example 278 86Example 279 11 Example 280 16 Example 281 16 Example 282 73 Example 28321 Example 284 25 Example 285 140 Example 286 93 Example 287 5 Example288 16 Example 289 23 Example 290 170 Example 291 110 Example 292 240Example 293 570 Example 294 1400 Example 295 13 Example 296 117 Example297 1430 Example 298 17 Example 299 5 Example 300 88 Example 301 92Example 302 9 Example 303 47 Example 304 6 Example 305 27 Example 306 60Example 307 560 Example 308 23 Example 309 44 Example 310 21 Example 311340 Example 312 10 Example 313 36 Example 314 9 Example 315 99 Example316 81 Example 317 450 Example 318 790 Example 319 82 Example 320 71Example 321 16 Example 322 4 Example 323 660 Example 324 270 Example 3251100 Example 326 4 Example 327 4 Example 328 4 Example 329 67 Example330 22 Example 331 2800 Example 332 1900 Example 333 54 Example 334 41Example 335 51 Example 336 1650 Example 337 66 Example 338 7 Example 3398 Example 340 12 Example 341 17 Example 342 2 Example 343 6 Example 3445 Example 345 7 Example 346 4 Example 347 23 Example 348 15 Example 34949 Example 350 1300 Example 351 65 Example 352 25 Example 353 5 Example354 135 Example 355 20 Example 356 2 Example 357 32 Example 358 10Example 359 15 Example 360 6 Example 361 31 Example 362 220 Example 363150 Example 364 5 Example 365 61 Example 366 150 Example 367 40 Example368 7 Example 369 420 Example 370 2400 Example 371 240 Example 372 7Example 373 5 Example 374 63 Example 375 40 Example 376 8 Example 377205 Example 378 2550 Example 379 880 Example 380 170 Example 381 8Example 382 35 Example 383 5 Example 384 30 Example 385 4 Example 386 12Example 387 70 Example 388 64 Example 389 130 Example 390 25 Example 39113 Example 392 18 Example 393 180 Example 394 71 Example 395 19 Example396 16 Example 397 92 Example 398 25 Example 399 6 Example 400 6 Example401 1400 Example 402 55 Example 403 12 Example 404 13 Example 405 14Example 406 3 Example 407 29 Example 408 6 Example 409 140 Example 410 2Example 411 150 Example 412 12 Example 413 4 Example 414 3 Example 4151150 Example 416 1150 Example 417 27 Example 418 65 Example 419 14Example 420 24 Example 421 410 Example 422 240 Example 423 55 Example424 370 Example 425 415 Example 426 59 Example 427 15 Example 428 550Example 429 17 Example 430 45 Example 431 69 Example 432 320 Example 4331500 Example 434 7 Example 435 5 Example 436 10 Example 437 21 Example438 16 Example 439 39 Example 440 97 Example 441 21 Example 442 8Example 443 11 Example 444 120 Example 445 12 Example 446 12 Example 447560 Example 448 440 Example 449 8 Example 450 660 Example 451 78 Example452 16 Example 453 18 Example 454 11 Example 455 165 Example 456 41Example 457 130 Example 458 1550 Example 459 46 Example 460 98 Example461 170 Example 462 25 Example 463 34 Example 464 2 Example 465 170Example 466 11 Example 467 69 Example 468 300 Example 469 5 Example 4703 Example 471 7 Example 472 880 Example 473 160 Example 474 234 Example475 215 Example 476 29 Example 477 98 Example 478 45 Example 479 18Example 480 375 Example 481 1400 Example 482 52 Example 483 1250 Example484 36 Example 485 1350 Example 486 59 Example 487 150 Example 488 65Example 489 270 Example 490 6 Example 491 220 Example 492 13 Example 493625 Example 494 190 Example 495 11 Example 496 230 Example 497 3 Example498 1310 Example 499 3150 Example 500 52 Example 501 5 Example 502 5Example 503 4 Example 504 5 Example 505 1200 Example 506 28 Example 4973 Example 498 1310 Example 499 3150 Example 500 52 Example 501 5 Example502 5 Example 503 4 Example 504 5 Example 505 1200 Example 506 28Example 509 10 Example 510 190 Example 511 120 Example 512 1400 Example513 7 Example 514 9 Example 515 110 Example 516 31 Example 517 29Example 518 14 Example 519 230 Example 520 1600 Example 521 8 Example522 910 Example 523 690 Example 524 8 Example 525 4 Example 526 17Example 527 9 Example 528 4 Example 529 2700 Example 530 33 Example 5311500 Example 532 2800 Example 533 2000 Example 534 1500 Example 535 26Example 536 17 Example 537 26 Example 538 12 Example 539 20 Example 54017 Example 541 260 Example 542 28 Example 543 480 Example 544 11 Example545 14 Example 546 14 Example 547 29 Example 548 790 Example 549 2600Example 550 500 Example 551 1900 Example 552 15 Example 553 7.2 Example554 1.9 Example 555 1.6 Example 556 810 Example 557 1000 Example 558 80Example 559 110Biological in vivo assays

The in vivo activity of the compounds of the present invention can bedemonstrated in the following assays:

FGFR Induced Calcification Model (Rat)

The aim of this study was to test the effect of Npt2a antagonists onvascular and soft tissue calcification and plasma levels of FGF-23,parathyroid hormone and phosphate in FGFR inhibitor inducedcalcification model in rats.

All rat experiments were conducted in accordance with Europeanguidelines for the use of experimental animals and in accordance withthe German Animal Protection Act (Deutsches Tierschutzgesetz).

Briefly, male Wistar Unilever (WU) rats were housed under normalconditions for laboratory rats in a 12:12-h light:dark cycle. Vascularand soft tissue calcification was induced by application of a FGFRinhibitor by once daily oral gavage for up to 2 weeks. The respectiveNpt2a inhibitor was also applied as indicated in the respective graphonce or twice daily (QD or BID) by oral gavage for the same duration asthe FGFR inhibitor. Blood samples were withdrawn during the study periodand at the end of the study to determine the plasma levels of FGF-23,parathyroid hormone and phosphate with commercial available assaysystems according to the manufactures protocols (e.g.FGF-23: Mouse/RatFGF-23(C-Term) ELISA Kit; Immuntopics; phosphate: Pentra400 system,parathyroid hormone: PTH 1-84 Bioactive, rat).

At the end of the study animals were sacrificed and the organs (e.g.heart, aorta, kidney, stomach) withdrawn. To determine the calcificationof the respective organs either von Kossa staining or H&E staining wasdone on histological preparations of the organs or an ashing of theorgans was done followed by flame photometry to determine the calciumcontent in the organ proportionally to the wet weight of the organ.

1.-14. (canceled)
 15. A method for treatment of a disease or conditionassociated with hyperphosphatemia, elevated plasma FGF23 levels,disbalanced phosphate homeostasis, or chronic kidney disease (CKD), in apatient in need thereof, comprising administering to said patient acompound of formula (I):

wherein R¹ is a group of the formula

wherein # is the point of attachment to the amino group, R⁵ is a groupselected from a halogen atom, cyano, (C₁-C₄)-alkyl, (C₁-C₄)-alkoxy,(C₃-C₆)-cycloalkyl, 4- to 6-membered heterocycle and(C₁-C₄)-alkylcarbonyl, wherein said (C₁-C₄)-alkyl is optionallysubstituted, identically or differently, with one or two groups selectedfrom —NR¹⁴R¹⁵, (C₁-C₄)-alkoxy and cyclopropyl and optionally up to fivefluorine atoms, wherein said cyclopropyl is optionally substituted withup to four fluorine atoms, wherein R¹⁴ is a hydrogen atom or(C₁-C₄)-alkyl, R¹⁵ is a hydrogen atom or (C₁-C₄)-alkyl, or R¹⁴ and R¹⁵together with the nitrogen atom they are attached form a 4- to5-membered heterocycle wherein said 4- to 5-membered heterocycle isoptionally substituted, identically or differently, with one, two orthree groups selected from (C₁-C₄)-alkyl trifluormethyl, difluoromethyland optionally up to five fluorine atoms, wherein said (C₁-C₄)-alkoxy isoptionally substituted with up to three fluorine atoms, wherein said 4-to 6-membered heterocycle is optionally substituted, identically ordifferently, with one or two groups selected from (C₁-C₄)-alkyl andoptionally up to five fluorine atoms, wherein said (C₃-C₆)-cycloalkyl isoptionally substituted, identically or differently, with one or twogroups selected from (C₁-C₄)-alkyl and optionally up to five fluorineatoms, R⁶ is 6-membered heteroaryl, 2-oxopyridin-1(2H)-yl, a 4- to8-membered heterocycle or (C₄-C₈)-cycloalkyl, or is a group of theformula

wherein ## is the point of attachment to the pyrazole ring, R³⁸ is ahydrogen atom, halogen or methyl, R^(38a) is a hydrogen atom, halogen ormethyl, R³⁹ is a hydrogen atom, cyano, fluorine or(C₁-C₄)-alkylsulfanyl, R^(39a) is a hydrogen atom, cyano, fluorine or(C₁-C₄)-alkylsulfanyl, R⁴⁰ is a hydrogen atom, halogen, cyano, hydroxy,—(CH₂)_(n)NR¹⁶R¹⁷, (C₁-C₄)-alkyl, (C₁-C₄)-alkoxy or(C₁-C₄)-alkoxycarbonyl, wherein said (C₁-C₄)-alkyl is optionallysubstituted with cyano and optionally with up to five fluorine atoms,wherein said (C₁-C₄)-alkoxy is optionally substituted with up to fivefluorine atoms, wherein n is 0 or 1, R¹⁶ is a hydrogen atom or(C₁-C₄)-alkyl, wherein said (C₁-C₄)-alkyl is optionally substituted withup to five fluorine atoms, R¹⁷ is a hydrogen atom or (C₁-C₄)-alkyl,wherein said (C₁-C₄)-alkyl is optionally substituted with up to fivefluorine atoms, or R¹⁶ and R¹⁷ together with the nitrogen atom they areattached form a 4- to 8-membered heterocycle wherein said 4- to8-membered heterocycle is optionally substituted, identically ordifferently, with one, two or three groups selected from (C₁-C₄)-alkyland optionally up to five fluorine atoms, wherein said 6-memberedheteroaryl group is optionally substituted, identically or differently,with one or two groups selected from a halogen atom, cyano,(C₁-C₄)-alkyl, and (C₁-C₄)-alkoxy, wherein said (C₁-C₄)-alkyl isoptionally substituted with up to five fluorine atoms, wherein said(C₁-C₄)-alkoxy is optionally substituted with up to three fluorineatoms, wherein said 2-oxopyridin-1(2H)-yl is optionally substituted,identically or differently, with one or two groups selected from ahalogen atom, cyano, (C₁-C₄)-alkyl and (C₁-C₄)-alkoxy, wherein said(C₁-C₄)-alkyl is optionally substituted with up to five luorine atoms,wherein said (C₁-C₄)-alkoxy is optionally substituted with up to threefluorine atoms, wherein said 4- to 8-membered heterocycle is optionallysubstituted, identically or differently, with one, two or three groupsselected from (C₁-C₄)-alkyl, cyano, (C₁-C₄)-alkoxycarbonyl andoptionally up to five fluorine atoms, wherein said (C₁-C₄)-alkyl isoptionally substituted with up to five fluorine atoms, wherein said(C₄-C₈)-cycloalkyl is optionally substituted, identically ordifferently, with one or two groups selected from (C₁-C₄)-alkyl, cyanoand optionally up to five fluorine atoms, wherein said (C₁-C₄)-alkyl isoptionally substituted with (C₃-C₆)-cycloalkyl and optionally up to fivefluorine atoms, R⁷ is a hydrogen atom, (C₁-C₄)-alkyl, a phenyl group, a5- to 6-membered heteroaryl group or (C₁-C₄)-alkyl sulfonyl, wherein anyphenyl group and any 5- to 6-membered heteroaryl are each optionallysubstituted, identically or differently, with one, two or three groupsselected from a halogen atom, (C₁-C₄)-alkyl, trifluoromethyl,(C₁-C₄)-alkoxy and trifluoromethoxy, wherein said (C₁-C₄)-alkyl isoptionally substituted with a group selected from (C₃-C₆)-cycloalkyl, 4-to 6-membered heterocycle, hydroxy, —NR²⁰R²¹, (C₁-C₄)-alkoxy orbenzyloxy and optionally with up to five fluorine atoms, wherein said(C₃-C₆)-cycloalkyl is optionally substituted, identically ordifferently, with one or two groups selected from (C₁-C₄)-alkyl, hydroxyand up to five fluorine atoms, wherein said 4- to 6-membered heterocycleis optionally substituted, identically or differently, with one or twogroups selected from (C₁-C₄)-alkyl and optionally up to five fluorineatoms, and wherein R²⁰ is a hydrogen atom or (C₁-C₄)-alkyl, R²¹ is ahydrogen atom or (C₁-C₄)-alkyl, or R²⁰ and R²¹ together with thenitrogen atom they are attached form a 4- to 6-membered heterocyclewherein said 4- to 6-membered heterocycle is optionally substituted,identically or differently, with one, two or three groups selected from(C₁-C₄)-alkyl and optionally up to five fluorine atoms, with the provisothat if R⁵ is (C₁-C₄)-alkoxy then R⁷ is different from hydrogen, withthe proviso that if R⁶ is 6-membered heteroaryl then R⁷ is differentfrom hydrogen, with the proviso that if R⁶ is 2-oxopyridin-1(2H)-yl thenR⁷ is different from hydrogen, with the proviso that if R⁶ is a 4- to8-membered heterocycle then R⁷ is different from hydrogen, R⁸ is a groupselected from a halogen atom, cyano, (C₁-C₄)-alkyl, (C₁-C₄)-alkoxy,(C₃-C₆)-cycloalkyl, 4- to 6-membered heterocycle, (C₁-C₄)-alkylcarbonyland a phenyl group, wherein said (C₁-C₄)-alkyl is optionallysubstituted, identically or differently, with one or two groups selectedfrom —NR²²R²³ (C₁-C₄)-alkoxy and cyclopropyl and optionally up to fivefluorine atoms, wherein said cyclopropyl is optionally substituted withup to four fluorine atoms, wherein said (C₁-C₄)-alkoxy is optionallysubstituted with up to five fluorine atoms, wherein R²² is a hydrogenatom or (C₁-C₄)-alkyl, R²³ is a hydrogen atom or (C₁-C₄)-alkyl, or R²²and R²³ together with the nitrogen atom they are attached form a 4- to6-membered heterocycle wherein said 4- to 6-membered heterocycle isoptionally substituted, identically or differently, with one, two orthree groups selected from (C₁-C₄)-alkyl and optionally up to fivefluorine atoms, wherein said (C₁-C₄)-alkoxy is optionally substitutedwith up to five fluorine atoms, wherein said (C₃-C₆)-cycloalkyl isoptionally substituted, identically or differently, with one or twogroups selected from (C₁-C₄)-alkyl and optionally up to five fluorineatoms, wherein said 4- to 6-membered heterocycle is optionallysubstituted, identically or differently, with one or two groups selectedfrom (C₁-C₄)-alkyl and optionally up to five fluorine atoms, and whereinsaid phenyl group is optionally substituted, identically or differently,with one, two or three groups selected from a halogen atom, cyano,(C₁-C₄)-alkyl, trifluoromethyl, (C₁-C₄)-alkoxy and trifluoromethoxy, R⁹is 6-membered heteroaryl, 2-oxopyridin-1(2H)-yl, (C₃-C₈)-cycloalkyl, a4- to 8-membered heterocycle or (C₁-C₄)-alkyl, or is a group of theformula

wherein ## is the point of attachment to the pyrazole ring, R^(38b) is ahydrogen atom, halogen or methyl, R^(38c) is a hydrogen atom, halogen ormethyl, R^(39b) is a hydrogen atom, cyano, fluorine or(C₁-C₄)-alkylsulfanyl, R^(39c) is a hydrogen atom, cyano, fluorine or(C₁-C₄)-alkylsulfanyl, R^(40a) is a hydrogen atom, halogen, cyano,hydroxy, —(CH₂)_(n)NR^(16a)R^(17a), (C₁-C₄)-alkyl, (C₁-C₄)-alkoxy,(C₁-C₄)-alkoxycarbonyl, a 4- to 6-membered heterocycle, cyclopropyl orcyclobutyl, wherein said (C₁-C₄)-alkyl is optionally substituted withcyano and optionally with up to five fluorine atoms, wherein said(C₁-C₄)-alkoxy is optionally substituted with up to five fluorine atoms,wherein said 4- to 6-membered heterocycle is optionally substituted,identically or differently, with one, two or three groups selected from(C₁-C₄)-alkyl and optionally up to five fluorine atoms, wherein n is 0or 1, R^(16a) is a hydrogen atom or (C₁-C₄)-alkyl, wherein said(C₁-C₄)-alkyl is optionally substituted with up to five fluorine atoms,R^(17a) is a hydrogen atom or (C₁-C₄)-alkyl, wherein said (C₁-C₄)-alkylis optionally substituted with up to five fluorine atoms, or R^(16a) andR^(17a) together with the nitrogen atom they are attached form a 4- to8-membered heterocycle wherein said 4- to 8-membered heterocycle isoptionally substituted, identically or differently, with one, two orthree groups selected from (C₁-C₄)-alkyl and optionally up to fivefluorine atoms, wherein said (C₁-C₄)-alkyl is optionally substitutedwith up to five fluorine atoms, wherein said 6-membered heteroaryl groupis optionally substituted, identically or differently, with one or twogroups selected from a halogen atom, cyano, (C₁-C₄)-alkyl, and(C₁-C₄)-alkoxy, wherein said (C₁-C₄)-alkyl is optionally substitutedwith up to five fluorine atoms, wherein said (C₁-C₄)-alkoxy isoptionally substituted with up to three fluorine atoms, wherein said2-oxopyridin-1(2H)-yl is optionally substituted, identically ordifferently, with one or two groups selected from a halogen atom, cyano,(C₁-C₄)-alkyl, and (C₁-C₄)-alkoxy, wherein said (C₁-C₄)-alkyl isoptionally substituted with up to five fluorine atoms, wherein said(C₁-C₄)-alkoxy is optionally substituted with up to three fluorineatoms, wherein said (C₃-C₈)-cycloalkyl is optionally substituted,identically or differently, with one or two groups selected from(C₁-C₄)-alkyl, cyano and optionally up to five fluorine atoms, whereinsaid (C₁-C₄)-alkyl is optionally substituted with (C₃-C₆)-cycloalkyl andoptionally up to five fluorine atoms, wherein said 4- to 8-memberedheterocycle is optionally substituted identically or differently, withone or two groups selected from (C₁-C₄)-alkyl, cyano,(C₁-C₄)-alkoxycarbonyl and optionally up to five fluorine atoms, whereinsaid (C₁-C₄)-alkyl is optionally substituted with up to five fluorineatoms, R¹⁰ is a hydrogen atom, (C₁-C₄)-alkyl, (C₃-C₅)-cycloalkyl,(C₁-C₄)-alkoxycarbonyl, mono-(C₁-C₄)-alkylamino, a phenyl group or a 5-to 6-membered heteroaryl group, wherein any phenyl group and any 5- to6-membered heteroaryl are each optionally substituted, identically ordifferently, with one, two or three groups selected from a halogen atom,(C₁-C₄)-alkyl, trifluoromethyl, (C₁-C₄)-alkoxy and trifluoromethoxy,wherein said (C₁-C₄)-alkyl is optionally substituted with a groupselected from (C₃-C₆)-cycloalkyl, 5-membered heteroaryl, —NR²⁸R²⁹,(C₁-C₄)-alkoxy or benzyloxy and optionally with up to five fluorineatoms and is optionally additionally substituted with hydroxy, whereinsaid (C₃-C₆)-cycloalkyl is optionally substituted, identically ordifferently, with hydroxy or one or two groups (C₁-C₄)-alkyl andoptionally up to five fluorine atoms, and wherein R²⁸ is a hydrogen atomor (C₁-C₄)-alkyl, R²⁹ is a hydrogen atom or (C₁-C₄)-alkyl, or R²⁸ andR²⁹ together with the nitrogen atom they are attached form a 4- to6-membered heterocycle wherein said 4- to 6-membered heterocycle isoptionally substituted, identically or differently, with one, two orthree groups selected from (C₁-C₄)-alkyl and optionally up to fivefluorine atoms, wherein said 5-membered heteroaryl is optionallysubstituted with (C₁-C₄)-alkyl, with the proviso that if R⁹ is6-membered heterorayl then R^(m) is different from hydrogen, with theproviso that if R⁹ is 2-oxopyridin-1(2H)-yl then R¹⁰ is different fromhydrogen, with the proviso that if R⁹ is a 4- to 8-membered heterocyclethen R¹⁰ is different from hydrogen, with the proviso that if R⁸ is(C₁-C₄)-alkoxy then R¹⁰ is different from hydrogen, R¹¹ is a groupselected from a hydrogen atom, a fluorine atom, a chlorine atom,(C₁-C₄)-alkyl and cyclopropyl, wherein said (C₁-C₄)-alkyl is optionallysubstituted with cyclopropyl and optionally up to five fluorine atoms,R¹² is a 6-membered heteroaryl group, 2-oxopyridin-1(2H)-yl,(C₄-C₈)-cycloalkyl or (C₁-C₄)-alkyl, or is a group of the formula

wherein ## is the point of attachment to the pyrazole ring, R^(38d) is ahydrogen atom, halogen or methyl, R^(38e) is a hydrogen atom, halogen ormethyl, R^(39d) is a hydrogen atom, cyano, fluorine or(C₁-C₄)-alkylsulfanyl, R^(39e) is a hydrogen atom, cyano, fluorine or(C₁-C₄)-alkylsulfanyl, R^(40b) is a hydrogen atom, halogen, cyano,hydroxy, —(CH₂)_(n)NR^(16a)R^(17a), (C₁-C₄)-alkyl, (C₁-C₄)-alkoxy,(C₁-C₄)-alkoxycarbonyl, a 4- to 6-membered heterocycle, cyclopropyl orcyclobutyl, wherein said (C₁-C₄)-alkyl is optionally substituted withcyano and optionally with up to five fluorine atoms, wherein said(C₁-C₄)-alkoxy is optionally substituted with up to five fluorine atoms,wherein said 4- to 6-membered heterocycle is optionally substituted,identically or differently, with one, two or three groups selected from(C₁-C₄)-alkyl and optionally up to five fluorine atoms, wherein n is 0or 1, R^(16a) is a hydrogen atom or (C₁-C₄)-alkyl, wherein said(C₁-C₄)-alkyl is optionally substituted with up to five fluorine atoms,R^(17a) is a hydrogen atom or (C₁-C₄)-alkyl, wherein said (C₁-C₄)-alkylis optionally substituted with up to five fluorine atoms, or R^(16a) andR^(17a) together with the nitrogen atom they are attached form a 4- to8-membered heterocycle wherein said 4- to 8-membered heterocycle isoptionally substituted, identically or differently, with one, two orthree groups selected from (C₁-C₄)-alkyl and optionally up to fivefluorine atoms, wherein said 6-membered heteroaryl group is optionallysubstituted, identically or differently, with one or two groups selectedfrom a halogen atom, cyano, (C₁-C₄)-alkyl, and (C₁-C₄)-alkoxy, whereinsaid (C₁-C₄)-alkyl is optionally substituted with up to five fluorineatoms, wherein said (C₁-C₄)-alkoxy is optionally substituted with up tothree fluorine atoms, wherein said 2-oxopyridin-1(2H)-yl is optionallysubstituted, identically or differently, with one or two groups selectedfrom a halogen atom, cyano, (C₁-C₄)-alkyl, and (C₁-C₄)-alkoxy, whereinsaid (C₁-C₄)-alkyl is optionally substituted with up to five fluorineatoms, wherein said (C₁-C₄)-alkoxy is optionally substituted with up tothree fluorine atoms, wherein said (C₄-C₈)-cycloalkyl is optionallysubstituted, identically or differently, with one or two groups selectedfrom (C₁-C₄)-alkyl or cyano and optionally up to five fluorine atoms,R¹³ is a group selected from a hydrogen atom, a fluorine atom, achlorine atom, (C₁-C₄)-alkyl and cyclopropyl, wherein said (C₁-C₄)-alkylis optionally substituted with cyclopropyl and up to five fluorineatoms, R² is a group selected from a hydrogen atom, (C₁-C₄)-alkyl,(C₃-C₆)-cycloalkyl and (C₁-C₄)-alkoxycarbonyl, wherein said(C₁-C₄)-alkyl is optionally substituted, identically or differently,with one or two groups selected from hydroxy, (C₁-C₄)-alkoxy,cyclopropyl and optionally up to five fluorine atoms, R³ is a groupselected from a hydrogen atom, a halogen atom, cyano, hydroxy, nitro,amino, mono-(C₁-C₄)-alkylamino, di-(C₁-C₄)-alkylamino,(C₁-C₄)-alkylsulfanyl, (C₁-C₄)-alkylsulfinyl, (C₁-C₄)-alkylsulfonyl,(C₁-C₆)-alkyl, (C₁-C₄)-alkoxy, (C₃-C₆)-cycloalkyl, 4- to 6-memberedheterocycle, 5- to 6-membered heteroaryl, —(CH₂)_(q)C(═O)—NR³⁴R³⁵,−O—C(═O)—NR³⁶R³⁷, −O—C(═O)—OR^(37a), —NH—C(═O)—NR³⁶R³⁷,—N(CH₃)—C(═O)—NR³⁶R³⁷, —NH—C(═O)—OR^(37a),—N(CH₃)—C(═O)—OR^(37a)—NH—C(═O)—R³⁷, —N(CH₃)—C(═O)—R³⁷,(C₁-C₄)-alkylcarbonyl, (C₁-C₄)-alkylcarbonyloxy and(C₁-C₄)-alkoxycarbonyl, wherein said (C₁-C₆)-alkyl is optionallysubstituted, identically or differently, with one or two groups selectedfrom hydroxy, amino, mono-(C₁-C₄)-alkylamino, di-(C₁-C₄)-alkylamino,cyano, (C₁-C₄)-alkoxy, 4- to 6-membered heterocycle,(C₁-C₄)-alkoxycarbonyl and cyclopropyl and optionally up to six fluorineatoms, wherein said 4- to 6-membered heterocycle is optionallysubstituted with (C₁-C₄)-alkyl or cyclopropyl and optionally up to twofluorine atoms, wherein said (C₁-C₄)-alkoxy is optionally substitutedwith cyano, cyclopropyl and optionally up to five fluorine atoms,wherein said (C₁-C₄)-alkyl of mono-(C₁-C₄)-alkylamino is optionallysubstituted with cyano, cyclopropyl and optionally up to five fluorineatoms, wherein said di-(C₁-C₄)-alkylamino is optionally substituted withcyano, cyclopropyl and optionally up to five fluorine atoms, whereinsaid (C₃-C₆)-cycloalkyl is optionally substituted, identically ordifferently, with one or two groups selected from (C₁-C₄)-alkyl,(C₁-C₄)-alkoxy, hydroxy and cyclopropyl and optionally up to fivefluorine atoms, wherein said 4- to 6-membered heterocycle is optionallysubstituted, identically or differently, with one or two groups selectedfrom (C₁-C₄)-alkyl, trifluoromethyl, difluoromethyl, (C₁-C₄)-alkoxy,(C₁-C₄)-alkoxycarbonyl, mono-(C₁-C₄)-alkylaminocarbonyl,di-(C₁-C₄)-alkylaminocarbonyl, (C₁-C₄)-alkylcarbonyl, hydroxy andcyclopropyl and optionally up to five fluorine atoms, wherein said 5- to6-membered heteroaryl is optionally substituted, identically ordifferently, with one or two groups selected from (C₁-C₄)-alkyl,(C₁-C₄)-alkoxy, and cyclopropyl and optionally up to five fluorineatoms, wherein q is 0 or 1, R³⁴ is a hydrogen atom or (C₁-C₄)-alkyl, R³⁵is a hydrogen atom, (C₁-C₄)-alkyl or phenyl, or R³⁴ and R³⁵ togetherwith the nitrogen atom they are attached form a 4- to 7-memberedheterocyclyl ring wherein said 4- to 7-membered heterocyclyl ring isoptionally substituted, identically or differently, with one, two orthree groups selected from a fluorine atom, hydroxy, (C₁-C₄)-alkyl,(C₁-C₄)-alkoxy, cyclopropyl, difluoromethyl, trifluoromethyl andtrifluoromethoxy, wherein R³⁶ is a hydrogen atom or methyl, R³⁷ is ahydrogen atom, methyl, difluoromethyl, trifluoromethyl or cyclopropyl,R^(37a) is methyl, difluoromethyl, trifluoromethyl or cyclopropyl, withthe proviso that if R³ is —(CH₂)_(q)C(═O)—NR³⁴R³⁵, —O—C(═O)—NR³⁶R³⁷,—O—C(═O)—OR^(37a), —N(CH₃)—C(═O)—NR³⁶R³⁷, —NH—C(═O)—OR^(37a),—NH—C(═O)—NR³⁶R³⁷, —N(CH₃)—C(═O)—OR^(37a)—NH—C(═O)—R³⁷ or—N(CH₃)—C(═O)—R³⁷, then R⁷ and R¹⁰ are different from hydrogen, with theproviso that if R³ is cyano then R² and R⁴ are different from hydrogen,with the proviso that if R³ is cyano then R⁶ and R⁹ are different from6-membered heteroaryl, or R² and R³ together with the carbon atoms theyare attached form a 4- to 6-membered carbocycle, a 4- to 7-memberedazaheterocycle, a 4- to 7-membered oxaheterocycle, a 5- to 6-memberedheteroaryl group or a phenyl ring, wherein said 4- to 7-memberedazaheterocycle is optionally substituted, identically or differently,with one or two groups selected from hydroxy, oxo, (C₁-C₄)-alkyl,trifluoromethyl, (C₁-C₄)-alkylcarbonyl and (C₁-C₄)-alkoxycarbonyl andoptionally up to five fluorine atoms, wherein said 4- to 7-memberedoxaheterocycle is optionally substituted, identically or differently,with one or two groups selected from hydroxy, oxo, (C₁-C₄)-alkyl,trifluoromethyl, (C₁-C₄)-alkylcarbonyl and (C₁-C₄)-alkoxycarbonyl andoptionally up to five fluorine atoms, wherein said 4- to 6-memberedcarbocycle is optionally substituted, identically or differently, withone or two groups selected from hydroxy, oxo, amino,mono-(C₁-C₄)-alkylamino, di-(C₁-C₄)-alkylamino, (C₁-C₄)-alkyl,trifluoromethyl, (C₁-C₄)-alkylcarbonyl and (C₁-C₄)-alkoxycarbonyl andoptionally up to five fluorine atoms, and wherein any phenyl group andany 5- to 6-membered heteroaryl group are each optionally substituted,identically or differently, with one, two or three groups selected froma halogen atom, (C₁-C₄)-alkyl, trifluoromethyl, (C₁-C₄)-alkoxy andtrifluoromethoxy, with the proviso that if R² and R³ together with thecarbon atoms they are attached to form a 4- to 7-membered azaheterocyclewith a non-substituted nitrogen atom which is not directly attached tothe pyrazole, then R⁷ and R^(l)° are different from hydrogen, with theproviso that if R⁷ and R¹⁰ are hydrogen then the nitrogen atom of the 4-to 7-membered azaheterocycle formed by R² and R³ together with thecarbon atoms they are attached to is substituted with (C₁-C₄)-alkyl or(C₁-C₄)-alkoxycarbonyl, R⁴ is a group selected from a hydrogen atom,(C₁-C₄)-alkyl, (C₃-C₆)-cycloalkyl and (C₁-C₄)-alkoxycarbonyl andhydroxy, wherein said (C₁-C₄)-alkyl is optionally substituted,identically or differently, with one or two groups selected fromhydroxy, (C₁-C₄)-alkoxy and cyclopropyl and optionally up to fivefluorine atoms, or R³ and R⁴ together with the carbon atoms they areattached form a 4- to 6-membered carbocycle, a 4- to 7-memberedheterocycle, a 5- to 6-membered heteroaryl group or a phenyl ring,wherein said 4- to 7-membered heterocycle is optionally substituted,identically or differently, with one or two groups selected from afluorine atom, hydroxy, oxo, (C₁-C₄)-alkyl, trifluoromethyl,(C₁-C₄)-alkylcarbonyl and (C₁-C₄)-alkoxycarbonyl and optionally up tofive fluorine atoms, wherein said 4- to 6-membered carbocycle isoptionally substituted, identically or differently, with one or twogroups selected from a fluorine atom, hydroxy, oxo, (C₁-C₄)-alkyl,trifluoromethyl, (C₁-C₄)-alkylcarbonyl and (C₁-C₄)-alkoxycarbonyl andoptionally up to five fluorine atoms, and wherein any phenyl group andany 5- to 6-membered heteroaryl group are each optionally substituted,identically or differently, with one, two or three groups selected froma halogen atom, (C₁-C₄)-alkyl, trifluoromethyl, (C₁-C₄)-alkoxy andtrifluoromethoxy, with the proviso that if R³ and R⁴ together with thecarbon atoms they are attached form a 4- to 7-membered heterocycle witha non-substituted nitrogen atom which is not directly attached to thepyrazole, then R⁷ and R¹⁰ is different from hydrogen, with the provisothat if R⁷ and R¹⁰ are hydrogen then the nitrogen atom of the 4- to7-membered heterocycle formed by R³ and R⁴ together with the carbonatoms they are attached to is substituted with (C₁-C₄)-alkyl or(C₁-C₄)-alkoxycarbonyl, or a stereoisomer, a tautomer, an N-oxide, ahydrate, a solvate, or a salt thereof, or a mixture of same.
 16. Themethod of claim 15, wherein R¹ is a group of the formula

wherein # is the point of attachment to the amino group, R⁵ is a groupselected from fluorine, chlorine, cyano, (C₁-C₄)-alkyl, methoxy, ethoxy,(C₃-C₅)-cycloalkyl, methylcarbonyl and ethylcarbonyl, wherein said(C₁-C₄)-alkyl is optionally substituted, identically or differently,with one or two groups selected from —NR¹⁴R¹⁵, methoxy, ethoxy,difluoromethoxy, trifluoromethoxy and cyclopropyl and optionally up tofive fluorine atoms, wherein said cyclopropyl is optionally substitutedwith up to four fluorine atoms, wherein R¹⁴ is a hydrogen atom or(C₁-C₄)-alkyl, R¹⁵ is a hydrogen atom or (C₁-C₄)-alkyl, or R¹⁴ and R¹⁵together with the nitrogen atom they are attached form a 4- to5-membered heterocycle wherein said 4- to 5-membered heterocycle isoptionally substituted, identically or differently, with one or twogroups selected from (C₁-C₄)-alkyl, trifluormethyl, difluoromethyl andoptionally up to five fluorine atoms, wherein said methoxy and ethoxyare optionally substituted with up to three fluorine atoms, wherein said(C₃-C₅)-cycloalkyl is optionally substituted with up to four fluorineatoms, R⁶ is pyridyl, pyrimidyl, 2-oxopyridin-1(2H)-yl,(C₅-C₈)-cycloalkyl or a 6- to 8-membered heterocycle or is a group ofthe formula

wherein ## is the point of attachment to the pyrazole ring, R³⁸ is ahydrogen atom, halogen or methyl, R^(38a) is a hydrogen atom, halogen ormethyl, R³⁹ is a hydrogen atom, cyano, fluorine or(C₁-C₄)-alkylsulfanyl, R^(39a) is a hydrogen atom, cyano, fluorine or(C₁-C₄)-alkylsulfanyl, R⁴⁰ is a hydrogen atom, fluorine, chlorine,cyano, hydroxy, —(CH₂)_(n)NR¹⁶R¹⁷, (C₁-C₃)-alkyl, (C₁-C₃)-alkoxy or(C₁-C₄)-alkoxycarbonyl, wherein said (C₁-C₃)-alkyl is optionallysubstituted with cyano and optionally with up to five fluorine atoms,wherein said (C₁-C₃)-alkoxy is optionally substituted with up to fivefluorine atoms, wherein n is 0 or 1, R¹⁶ is a hydrogen atom or(C₁-C₄)-alkyl, R¹⁷ is a hydrogen atom or (C₁-C₄)-alkyl, or R¹⁶ and R¹⁷together with the nitrogen atom they are attached form a 4- to6-membered heterocycle wherein said 4- to 6-membered heterocycle isoptionally substituted, identically or differently, with one, two orthree groups selected from (C₁-C₄)-alkyl and optionally up to fivefluorine atoms, wherein said pyridyl and pyrimidyl are optionallysubstituted, identically or differently, with one or two groups selectedfrom a halogen atom, cyano, methyl, ethyl, methoxy and ethoxy, whereinsaid (C₁-C₄)-alkyl is optionally substituted with up to five fluorineatoms, wherein said methoxy and ethoxy are optionally substituted withup to three fluorine atoms, wherein said 2-oxopyridin-1(2H)-yl isoptionally substituted, identically or differently, with one or twogroups selected from fluorine, cyano, methyl, ethyl, methoxy and ethoxy,wherein said methyl and ethyl are optionally substituted with up tothree fluorine atoms, wherein said methoxy and ethoxy are optionallysubstituted with up to three fluorine atoms, wherein said 6- to8-membered heterocycle is optionally substituted, identically ordifferently, with one or two groups selected from (C₁-C₄)-alkyl, cyano,(C₁-C₄)-alkoxycarbonyl and optionally up to five fluorine atoms, whereinsaid (C₁-C₄)-alkyl is optionally substituted with up to three fluorineatoms, wherein said (C₅-C₈)-cycloalkyl is optionally substituted,identically or differently, with one or two groups selected from(C₁-C₄)-alkyl and cyano, and optionally up to five fluorine atoms,wherein said (C₁-C₄)-alkyl is optionally substituted with up to threefluorine atoms, R⁷ is a hydrogen atom, (C₁-C₄)-alkyl, methylsulfonyl orethylsulfonyl, wherein said (C₁-C₄)-alkyl is optionally substituted witha group selected from (C₃-C₆)-cycloalkyl, hydroxy, —NR²⁰R²¹, methoxy,ethoxy or benzyloxy and optionally with up to five fluorine atoms,wherein said (C₃-C₆)-cycloalkyl is optionally substituted with hydroxyand optionally up to four fluorine atoms, and wherein R²⁰ is a hydrogenatom or (C₁-C₄)-alkyl, R²¹ is a hydrogen atom or (C₁-C₄)-alkyl, with theproviso that if R⁵ is methoxy or ethoxy then R⁷ is different fromhydrogen, with the proviso that if R⁶ is pyridyl or pyrimidyl then R⁷ isdifferent from hydrogen, with the proviso that if R⁶ is2-oxopyridin-1(2H)-yl then R⁷ is different from hydrogen, with theproviso that if R⁶ is a 6- to 8-membered heterocycle then R⁷ isdifferent from hydrogen, R⁸ is a group selected from fluorine, chlorine,cyano, (C₁-C₄)-alkyl, methoxy, ethoxy, methylcarbonyl, ethylcarbonyl and(C₃-C₅)-cycloalkyl, wherein said (C₁-C₄)-alkyl is optionally substitutedwith methoxy, —NR²²R²³ and cyclopropyl and optionally up to fivefluorine atoms, wherein said cyclopropyl is optionally substituted withup to four fluorine atoms, wherein said methoxy is optionallysubstituted with up to three fluorine atoms, wherein R²² is a hydrogenatom or (C₁-C₄)-alkyl, R²³ is a hydrogen atom or (C₁-C₄)-alkyl, or R²²and R²³ together with the nitrogen atom they are attached form a 4- to6-membered heterocycle wherein said 4- to 6-membered heterocycle isoptionally substituted, identically or differently, with one, two orthree groups selected from (C₁-C₄)-alkyl and optionally up to fivefluorine atoms, wherein said methoxy and ethoxy are optionallysubstituted with up to three fluorine atoms, and wherein said(C₃-C₅)-cycloalkyl is optionally substituted with up to four fluorineatoms, R⁹ is pyridyl, pyrimidyl, 2-oxopyridin-1(2H)-yl,(C₅-C₈)-cycloalkyl or a 6- to 8-membered heterocycle or (C₁-C₄)-alkyl,or is a group of the formula

wherein ## is the point of attachment to the pyrazole ring, R^(38b) is ahydrogen atom, halogen or methyl, R^(38c) is a hydrogen atom, halogen ormethyl, R^(39b) is a hydrogen atom, cyano, fluorine or(C₁-C₄)-alkylsulfanyl, R^(39c) is a hydrogen atom, cyano, fluorine or(C₁-C₄)-alkylsulfanyl, R^(40a) is a hydrogen atom, fluorine, chlorine,cyano, hydroxy, —(CH₂)_(n)NR^(16a)R^(17a), (C₁-C₃)-alkyl,(C₁-C₃)-alkoxy, (C₁-C₄)-alkoxycarbonyl, a 4- to 6-membered heterocycle,cyclopropyl or cyclobutyl, wherein said (C₁-C₃)-alkyl is optionallysubstituted with cyano and optionally with up to five fluorine atoms,wherein said (C₁-C₃)-alkoxy is optionally substituted with up to fivefluorine atoms, wherein said 4- to 6-membered heterocycle is optionallysubstituted, identically or differently, with one, two or three groupsselected from (C₁-C₄)-alkyl and optionally up to five fluorine atoms,wherein n is 0 or 1, R^(16a) is a hydrogen atom or (C₁-C₄)-alkyl,R^(17a) is a hydrogen atom or (C₁-C₄)-alkyl, or R^(16a) and R^(17a)together with the nitrogen atom they are attached form a 4- to6-membered heterocycle wherein said 4- to 6-membered heterocycle isoptionally substituted, identically or differently, with one, two orthree groups selected from (C₁-C₄)-alkyl and optionally up to fivefluorine atoms, wherein said (C₁-C₄)-alkyl is optionally substitutedwith up to five fluorine atoms, wherein said pyridyl and pyrimidyl areoptionally substituted, identically or differently, with one or twogroups selected from a halogen atom, cyano, methyl, ethyl, methoxy andethoxy, wherein said methyl and ethyl is optionally substituted with upto three fluorine atoms, wherein said methoxy and ethoxy are optionallysubstituted with up to three fluorine atoms, wherein said2-oxopyridin-1(2H)-yl is optionally substituted, identically ordifferently, with one or two groups selected from fluorine, cyano,methyl, ethyl, methoxy and ethoxy, wherein said methyl and ethyl areoptionally substituted with up to three fluorine atoms, wherein saidmethoxy and ethoxy are optionally substituted with up to three fluorineatoms, wherein said 6- to 8-membered heterocycle is optionallysubstituted, identically or differently, with one or two groups selectedfrom methyl, ethyl, cyano and (C₁-C₄)-alkoxycarbonyl and optionally upto five fluorine atoms, wherein said methyl is optionally substitutedwith up to three fluorine atoms, wherein said (C₅-C₈)-cycloalkyl isoptionally substituted, identically or differently, with one or twogroups selected from methyl, ethyl and cyano, and optionally up to fivefluorine atoms, wherein said methyl is optionally substituted with up tothree fluorine atoms, R¹⁰ is a hydrogen atom, (C₁-C₄)-alkyl or(C₃-C₅)-cycloalkyl, wherein said (C₁-C₄)-alkyl is optionally substitutedwith a group selected from (C₃-C₆)-cycloalkyl,2-methyl-2H-tetrazol-5-yl, 1-methyl-1H-tetrazol-5-yl, —NR²⁸R²⁹, methoxy,ethoxy or benzyloxy and optionally with up to five fluorine atomsoptionally with up to five fluorine atoms and is optionally additionallysubstituted with hydroxy, wherein said (C₃-C₆)-cycloalkyl is optionallysubstituted with up to four fluorine atoms, and wherein R²⁸ is ahydrogen atom or (C₁-C₄)-alkyl, R²⁹ is a hydrogen atom or (C₁-C₄)-alkyl,with the proviso that if R⁹ is pyridyl or pyrimidyl then R¹⁰ isdifferent from hydrogen, with the proviso that if R⁹ is2-oxopyridin-1(2H)-yl then R¹⁰ is different from hydrogen, with theproviso that if R⁹ is a 6- to 8-membered heterocycle then R¹⁰ isdifferent from hydrogen, with the proviso that if R⁸ is methoxy orethoxy then R¹⁰ is different from hydrogen, R¹¹ is a group selected froma hydrogen atom, (C₁-C₄)-alkyl and cyclopropyl, wherein said(C₁-C₄)-alkyl is optionally substituted with cyclopropyl and optionallywith up to five fluorine atoms, R¹² is pyridyl or 2-oxopyridin-1(2H)-yl,or is a group of the formula

wherein ## is the point of attachment to the pyrazole ring, R^(38d) is ahydrogen atom, fluorine or methyl, R^(38e) is a hydrogen atom, fluorineor methyl, R^(39d) is a hydrogen atom, cyano or fluorine, R^(39e) is ahydrogen atom, R^(40b) is a hydrogen atom, fluorine, chlorine, cyano,hydroxy, methyl, trifluoromethyl, methoxy, trifluoromethoxy ormethoxycarbonyl, wherein said pyridyl is optionally substituted,identically or differently, with one or two groups selected fromfluorine, cyano, methyl and methoxy, wherein said methyl is optionallysubstituted with up to three fluorine atoms, wherein said methoxy isoptionally substituted with up to three fluorine atoms, wherein said2-oxopyridin-1(2H)-yl is optionally substituted, identically ordifferently, with one or two groups selected from fluorine, cyano,methyl and methoxy, wherein said methyl is optionally substituted withup to three fluorine atoms, wherein said methoxy is optionallysubstituted with up to three fluorine atoms, R¹³ is a group selectedfrom a hydrogen atom, (C₁-C₄)-alkyl and cyclopropyl, wherein said(C₁-C₄)-alkyl is optionally substituted with cyclopropyl and optionallywith up to five fluorine atoms, R² is a group selected from a hydrogenatom, (C₁-C₄)-alkyl, cyclopropyl, methoxycarbonyl and ethoxycarbonyl,wherein said (C₁-C₄)-alkyl is optionally substituted, identically ordifferently, with one or two groups selected from hydroxy, methoxy,ethoxy, cyclopropyl and optionally up to five fluorine atoms, R³ is agroup selected from a hydrogen atom, fluorine, chlorine, bromine, cyano,hydroxy, nitro, amino, mono-(C₁-C₄)-alkylamino, di-(C₁-C₄)-alkylamino,(C₁-C₄)-alkylsulfanyl, (C₁-C₄)-alkylsulfinyl, (C₁-C₄)-alkylsulfonyl,(C₁-C₆)-alkyl, (C₁-C₄)-alkoxy, −O—C(═O)—NR³⁶R³⁷, −O—C(═O)—OR^(37a),—NH—C(═O)—NR³⁶R³⁷, —N(CH₃)—C(═O)—NR³⁶R³⁷, —NH—C(═O)—OR^(37a),—N(CH₃)—C(═O)—OR^(37a)—NH—C(═O)—R³⁷, —N(CH₃)—C(═O)—R³⁷,(C₃-C₅)-cycloalkyl, 4- to 6-membered heterocycle, 5- to 6-memberedheteroaryl, —(CH₂)_(q)—C(═O)—NR³⁴R³⁵, methylcarbonyl, ethylcarbonyl,(C₁-C₄)-alkylcarbonyloxy and (C₁-C₄)-alkoxycarbonyl, wherein said(C₁-C₆)-alkyl is optionally substituted, identically or differently,with one or two groups selected from hydroxy, amino,mono-(C₁-C₄)-alkylamino, di-(C₁-C₄)-alkylamino, cyano, methoxy, ethoxy,methoxycarbonyl, ethoxycarbony, 4- to 6-membered heterocycle, 1 andcyclopropyl and optionally up to five fluorine atoms, wherein said 4- to6-membered heterocycle is optionally substituted with methyl, ethyl orcyclopropyl and optionally up to two fluorine atoms, wherein said(C₁-C₄)-alkoxy is optionally substituted with cyano, cyclopropyl andoptionally up to five fluorine atoms, wherein said (C₃-C₅)-cycloalkyl isoptionally substituted with hydroxyl, methoxy, ethoxy and optionally upto four fluorine atoms, wherein said 4- to 6-membered heterocycle isoptionally substituted with hydroxyl, trifluoromethyl, methoxy, ethoxyand optionally up to four fluorine atoms, wherein said 5- to 6-memberedheteroaryl is optionally substituted, identically or differently, withone or two groups selected from methyl, ethyl and methoxy and optionallyup to four fluorine atoms, wherein q is 0, R³⁴ is a hydrogen atom or(C₁-C₄)-alkyl, R³⁵ is a hydrogen atom or (C₁-C₄)-alkyl, or R³⁴ and R³⁵together with the nitrogen atom they are attached form a 4- to7-membered heterocycle, wherein said 4- to 7-membered heterocyclel ringis optionally substituted, identically or differently, with one, two orthree groups selected from a fluorine atom, hydroxy, methyl, ethyl,methoxy, ethoxy, cyclopropyl, difluoromethyl, trifluoromethyl andtrifluoromethoxy, wherein R³⁶ is a hydrogen atom or methyl, R³⁷ is ahydrogen atom, methyl, difluoromethyl, trifluoromethyl or cyclopropyl,R^(37a) is methyl, difluoromethyl, trifluoromethyl or cyclopropyl, withthe proviso that if R³ is —(CH₂)_(q)C(═O)—NR³⁴R³⁵, −O—C(═O)—NR³⁶R³⁷,−O—C(═O)—OR^(37a), —N(CH₃)—C(═O)—NR³⁶R³⁷, —NH—C(═O)—OR^(37a),—NH—C(═O)—NR³⁶R³⁷, —N(CH₃)—C(═O)—OR^(37a), —NH—C(═O)—R³⁷ or—N(CH₃)—C(═O)—R³⁷, then R⁷ and R¹⁰ are different from hydrogen, with theproviso that if R³ is cyano then R² and R⁴ are different from hydrogen,with the proviso that if R³ is cyano then R⁶ and R⁹ are different from6-membered heteroaryl, or R² and R³ together with the carbon atoms theyare attached form a 5- to 6-membered carbocycle, a 5- to 7-memberedazaheterocycle, a 5- to 7-membered oxaheterocycle, a 5- to 6-memberedheteroaryl group or a phenyl ring, wherein said 5- to 7-memberedazaheterocycle is optionally substituted, identically or differently,with one or two groups selected from oxo, methyl, ethyl, propyl,trifluoromethyl and (C₁-C₄)-alkoxycarbonyl and optionally up to fourfluorine atoms, wherein said 5- to 7-membered oxaheterocycle isoptionally substituted, identically or differently, with one or twogroups selected from oxo, methyl, ethyl, trifluoromethyl and(C₁-C₄)-alkoxycarbonyl and optionally up to four fluorine atoms, whereinsaid 5- to 6-membered carbocycle is optionally substituted, identicallyor differently, with one or two groups selected from hydroxy, oxo,amino, mono-(C₁-C₄)-alkylamino, di-(C₁-C₄)-alkylamino, methyl, ethyl,trifluoromethyl and (C₁-C₄)-alkoxycarbonyl and optionally up to fourfluorine atoms, and wherein any phenyl group and any 5- to 6-memberedheteroaryl group are each optionally substituted, identically ordifferently, with one or two groups selected from fluorine, chlorine,methyl, ethyl, trifluoromethyl, methxoy and trifluoromethoxy, with theproviso that if R² and R³ together with the carbon atoms they areattached to form a 5- to 7-membered azaheterocycle with anon-substituted nitrogen atom which is not directly attached to thepyrazole, then R⁷ and R¹⁰ are different from hydrogen, with the provisothat if R⁷ and R¹⁰ are hydrogen then the nitrogen atom of the 5- to7-membered azaheterocycle formed by R² and R³ together with the carbonatoms they are attached to is substituted with methyl, ethyl or(C₁-C₄)-alkoxycarbonyl, R⁴ is a group selected from a hydrogen atom,(C₁-C₄)-alkyl, cyclopropyl, methoxycarbonyl, ethoxycarbonyl and hydroxy,wherein said (C₁-C₄)-alkyl is optionally substituted, identically ordifferently, with one or two groups selected from hydroxy, methoxy andcyclopropyl and optionally up to five fluorine atoms, or R³ and R⁴together with the carbon atoms they are attached form a 5- to 6-memberedcarbocycle, a 5- to 7-membered heterocycle, a 5- to 6-memberedheteroaryl group or a phenyl ring, wherein said 5- to 7-memberedheterocycle is optionally substituted, identically or differently, withone or two groups selected from oxo, methyl, ethyl, propyltrifluoromethyl and (C₁-C₄)-alkoxycarbonyl and optionally up to fourfluorine atoms, wherein said 5- to 6-membered carbocycle is optionallysubstituted, identically or differently, with one or two groups selectedfrom oxo, hydroxyl, methyl, ethyl, trifluoromethyl and(C₁-C₄)-alkoxycarbonyl and optionally up to four fluorine atoms, andwherein any phenyl group and any 5- to 6-membered heteroaryl group areeach optionally substituted, identically or differently, with one or twogroups selected from fluorine, chlorine, methyl, ethyl, trifluoromethyl,methoxy and trifluoromethoxy, with the proviso that if R³ and R⁴together with the carbon atoms they are attached form a 5- to 7-memberedheterocycle with a non-substituted nitrogen atom which is not directlyattached to the pyrazole, then R⁷ and R¹⁰ is different from hydrogen,with the proviso that if R⁷ and R¹⁰ are hydrogen then the nitrogen atomof the 5- to 7-membered heterocycle formed by R³ and R⁴ together withthe carbon atoms they are attached to is substituted with methyl, ethylor (C₁-C₄)-alkoxycarbonyl, or a stereoisomer, a tautomer, an N-oxide, ahydrate, a solvate, or a salt thereof, or a mixture of same.
 17. Themethod of claim 15, wherein: R¹ is a group of the formula

wherein # is the point of attachment to the amino group, R⁵ is a groupselected from chlorine, (C₁-C₄)-alkyl, methoxy, ethoxy and(C₃-C₅)-cycloalkyl, wherein said (C₁-C₄)-alkyl is optionally substitutedwith a group selected from methoxy, difluoromethoxy, trifluoromethoxy,—NR¹⁴R¹⁵, cyclopropyl or optionally with up to three fluorine atoms,wherein R¹⁴ is (C₁-C₄)-alkyl, R¹⁵ is (C₁-C₄)-alkyl, or R¹⁴ and R¹⁵together with the nitrogen atom they are attached form a 4- to6-membered heterocycle wherein said 4- to 6-membered heterocycle isoptionally substituted with methyl or trifluoromethyl or optionally withup to four fluorine atoms, wherein said methoxy and ethoxy areoptionally substituted with up to three fluorine atoms, wherein said(C₃-C₅)-cycloalkyl is optionally substituted with up to four fluorineatoms, R⁶ is pyridyl or (C₅-C₈)-cycloalkyl, or is a group of the formula

wherein ## is the point of attachment to the pyrazole ring, R³⁸ is ahydrogen atom, methyl or fluorine, R^(38a) is a hydrogen atom, R³⁹ is ahydrogen atom, cyano or fluorine, R^(39a) is a hydrogen atom, cyano,fluorine or methylsulfanyl, R⁴⁰ is a hydrogen atom, fluorine, chlorine,cyano, hydroxy, —(CH₂)_(n)NR¹⁶R¹⁷, methyl, methoxy, ethoxy,difluoromethoxy, trifluoromethoxy, methoxycarbonyl or ethoxycarbonyl,wherein said methyl is optionally substituted with cyano or optionallywith up to three fluorine atoms, wherein n is 0, R¹⁶ is a hydrogen atomor (C₁-C₄)-alkyl, R¹⁷ is (C₁-C₄)-alkyl, wherein said pyridyl isoptionally substituted, identically or differently, with one or twogroups selected from fluorine, cyano, methyl, methoxy and ethoxy,wherein said methyl is optionally substituted with up to three fluorineatoms, wherein said methoxy is optionally substituted with up to threefluorine atoms, wherein said (C₅-C₈)-cycloalkyl is optionallysubstituted, identically or differently, with one or two groups selectedfrom (C₁-C₄)-alkyl and cyano, or optionally with up to five fluorineatoms, wherein said (C₁-C₄)-alkyl is optionally substituted with up tothree fluorine atoms, R⁷ is a hydrogen atom or (C₁-C₄)-alkyl, whereinsaid (C₁-C₄)-alkyl is optionally substituted with (C₃-C₆)-cycloalkyl,methoxy or ethoxy or optionally with up to three fluorine atoms, withthe proviso that if R⁵ is methoxy, ethoxy, difluoromethoxy ortrifluoromethoxy then R⁷ is different from hydrogen, with the provisothat if R⁶ is pyridyl then R⁷ is different from hydrogen, R⁸ is a groupselected from chlorine, (C₁-C₄)-alkyl, methoxy, ethoxy and(C₃-C₅)-cycloalkyl, wherein said (C₁-C₄)-alkyl is optionally substitutedwith a group selected from methoxy —NR²²R²³, cyclopropyl or optionallywith up to three fluorine atoms, wherein said methoxy is optionallysubstituted with up to three fluorine atoms, wherein R²² is(C₁-C₄)-alkyl, R²³ is (C₁-C₄)-alkyl, wherein said methoxy and ethoxy areoptionally substituted with up to three fluorine atoms, and wherein said(C₃-C₅)-cycloalkyl is optionally substituted with up to four fluorineatoms, R⁹ is pyridyl or (C₅-C₈)-cycloalkyl, or is a group of the formula

wherein ## is the point of attachment to the pyrazole ring, R^(38b) is ahydrogen atom, methyl or fluorine, R^(38c) is a hydrogen atom orfluorine, R^(39b) is a hydrogen atom, cyano or fluorine, R^(39c) is ahydrogen atom, cyano or fluorine, R^(40a) is a hydrogen atom, fluorine,chlorine, cyano, hydroxy, —(CH₂)_(n)NR^(16a)R^(17a), methyl, methoxy,ethoxy, difluoromethoxy, trifluoromethoxy, methoxycarbonyl orethoxycarbonyl, a 4- to 6-membered heterocycle, cyclopropyl orcyclobutyl, wherein said methyl is optionally substituted with cyano oroptionally with up to three fluorine atoms, wherein n is 0, R^(16a) is ahydrogen atom, R^(17a) is (C₁-C₄)-alkyl, wherein said 4- to 6-memberedheterocycle is optionally substituted, with methyl or optionally with upto five fluorine atoms, wherein said pyridyl is optionally substituted,identically or differently, with one or two groups selected fromfluorine, cyano, methyl, methoxy and ethoxy, wherein said methyl isoptionally substituted with up to three fluorine atoms, wherein saidmethoxy and ethoxy are optionally substituted with up to three fluorineatoms, wherein said (C₅-C₈)-cycloalkyl is optionally substituted,identically or differently, with one or two groups selected from methyl,ethyl, cyano or optionally with up to five fluorine atoms, wherein saidmethyl is optionally substituted with up to three fluorine atoms, R¹⁰ isa hydrogen atom, (C₁-C₄)-alkyl or cyclopropyl, wherein said(C₁-C₄)-alkyl is optionally substituted with a group selected from(C₃-C₆)-cycloalkyl, methoxy, ethoxy, 2-methyl-2H-tetrazol-5-yl,1-methyl-1H-tetrazol-5-yl, —NR²⁸R²⁹ or optionally with up to threefluorine atoms and is optionally additionally substituted with hydroxy,wherein said (C₃-C₆)-cycloalkyl is optionally substituted with up tofour fluorine atoms, and wherein R²⁸ is a hydrogen atom or(C₁-C₄)-alkyl, R²⁹ is (C₁-C₄)-alkyl, with the proviso that if R⁹ ispyridyl then R¹⁰ is different from hydrogen, with the proviso that if R⁸is methoxy, ethoxy, difluoromethoxy or trifluoromethoxy then R¹⁰ isdifferent from hydrogen, R¹¹ is cyclopropyl, methyl or ethyl, whereinsaid methyl or ethyl are optionally substituted with cyclopropyl oroptionally with up to three fluorine atoms, R¹² is a group of theformula

wherein ## is the point of attachment to the pyrazole ring, R^(38d) is ahydrogen atom or fluorine, R^(38e) is a hydrogen atom, R^(39d) is ahydrogen atom or fluorine, R^(39e) is a hydrogen atom, R^(49b) is ahydrogen atom, fluorine, chlorine or cyano, R¹³ is a group selected froma hydrogen atom, methyl and cyclopropyl, wherein said methyl isoptionally substituted with cyclopropyl or optionally with up to threefluorine atoms, R² is a hydrogen atom or methyl, wherein said methyl isoptionally substituted with up to three fluorine atoms, R³ is a groupselected from a hydrogen atom, fluorine, chlorine, bromine, cyano,hydroxy, nitro, amino, m ono-(C₁-C₄)-alkyl amino, di-(C₁-C₄)-alkylamino, methyl sulfanyl, ethyl sulfanyl, methyl sulfinyl, ethyl sulfinyl,methyl sulfonyl, ethyl sulfonyl, —O—C(═O)—OR^(37a), —NH—C(═O)—NR³⁶R³⁷,—N(CH₃)—C(═O)—NR³⁶R³⁷, —NH—C(═O)—OR^(37a), (C₁-C₄)-alkyl, methoxy,ethoxy, (C₃-C₅)-cycloalkyl, 4- to 6-membered heterocycle, 5-memberedheteroaryl, —(CH₂)_(q)—C(═O)—NR³⁴R³⁵, methoxycarbonyl andethoxycarbonyl, wherein said (C₁-C₄)-alkyl is optionally substituted,identically or differently, with one or two groups selected fromhydroxy, cyano, methoxy, ethoxy, methoxycarbonyl, ethoxycarbonyl,methylamino, ethylamino, dimethylamino, diethylamino, a 4- to 6-memberedheterocycle and cyclopropyl and optionally up to three fluorine atoms,wherein said 4- to 6-membered heterocycle is optionally substituted withmethyl, ethyl or cyclopropyl and optionally up to two fluorine atoms,wherein said methoxy and ethoxy are optionally substituted with cyano,cyclopropyl or optionally up to three fluorine atoms, wherein said(C₃-C₅)-cycloalkyl is optionally substituted with hydroxy or optionallywith up to four fluorine atoms, wherein said 4- to 6-memberedheterocycle is optionally substituted with hydroxyl or trifluoromethylor optionally with up to four fluorine atoms, wherein said 5-memberedheteroaryl is optionally substituted, identically or differently, withone or two groups selected from methyl and methoxy wherein q is 0, R³⁴is a hydrogen atom or (C₁-C₄)-alkyl, R³⁵ is (C₁-C₄)-alkyl, or R³⁴ andR³⁵ together with the nitrogen atom they are attached form a 4- to6-membered heterocycle ring wherein said 4- to 6-membered heterocyclering is optionally substituted, identically or differently, with one ortwo groups selected from a fluorine atom, methyl, difluoromethyl,trifluoromethyl and trifluoromethoxy, wherein R³⁶ is a hydrogen atom ormethyl, R³⁷ is a hydrogen atom, methyl, difluoromethyl, trifluoromethylor cyclopropyl, R^(37a) is methyl, difluoromethyl, trifluoromethyl orcyclopropyl, with the proviso that if R³ is —(CH₂)_(q)C(═O)—NR³⁴R³⁵,–O—C(═O)—OR^(37a), —NH—C(═O)—NR³⁶R³⁷, —N(CH₃)—C(═O)—NR³⁶R³⁷ or—NH—C(═O)—OR^(37a), then R⁷ and R¹⁰ are different from hydrogen, withthe proviso that if R³ is cyano then R² and R⁴ are different fromhydrogen, with the proviso that if R³ is cyano then R⁶ and R⁹ aredifferent from pyridyl or pyrimidyl, or R² and R³ together with thecarbon atoms they are attached form a 4- to 6-membered carbocycle, a 5-to 6-membered azaheterocycle, a 5- to 6-membered oxaheterocycle, a6-membered heteroaryl group or a phenyl ring, wherein said phenyl groupis optionally substituted, identically or differently, with one or twogroups selected from fluorine, chlorine, methyl, trifluoromethyl,methxoy and trifluoromethoxy, wherein said 5- to 6-membered carbocycleis optionally substituted, identically or differently, with one or twogroups selected from hydroxy, oxo, methyl, ethyl, trifluoromethyl and(C₁-C₄)-alkoxycarbonyl or optionally with up to four fluorine atoms,wherein said 5- to 6-membered azaheterocycle is optionally substitutedwith oxo, methyl, ethyl, propyl, trifluoromethyl, tert.-butoxycarbonylor optionally with up to four fluorine atoms, wherein said 5- to6-membered oxaheterocycle is optionally substituted with oxo, methyl,ethyl, trifluoromethyl, methoxycarbonyl and ethoxycarbonyl or optionallywith up to four fluorine atoms, with the proviso that if R² and R³together with the carbon atoms they are attached to form a 5- to6-membered azaheterocycle with a non-substituted nitrogen atom which isnot directly attached to the pyrazole, then R⁷ and R¹⁰ are differentfrom hydrogen, with the proviso that if R⁷ and R¹⁰ are hydrogen then thenitrogen atom of the 5- to 6-membered azaheterocycle formed by R² and R³together with the carbon atoms they are attached to is substituted withmethyl, ethyl, methoxycarbonyl or ethoxycarbonyl, R⁴ is a group selectedfrom a hydrogen atom, (C₁-C₄)-alkyl, cyclopropyl, methoxycarbonyl,ethoxycarbonyl and hydroxy, wherein said (C₁-C₄)-alkyl is optionallysubstituted with a group selected from hydroxy, methoxy and cyclopropylor optionally with up to three fluorine atoms, or R³ and R⁴ togetherwith the carbon atoms they are attached form a 5- to 6-memberedcarbocycle, a 5- to 6-membered heterocycle, a 6-membered heteroarylgroup or a phenyl ring, wherein said 5- to 6-membered heterocycle isoptionally substituted, identically or differently, with one or twogroups selected from oxo, methyl, ethyl, propyl , trifluoromethyl,methoxycarbonyl, ethoxycarbonyl, tert.-butoxycarbonyl or optionally withup to four fluorine atoms, wherein said 5- to 6-membered carbocycle isoptionally substituted, identically or differently, with one or twogroups selected from oxo, hydroxy, methyl, ethyl, trifluoromethylmethoxycarbonyl and ethoxycarbonyl or optionally with up to fourfluorine atoms, and wherein any phenyl group and any 6-memberedheteroaryl group are each optionally substituted, identically ordifferently, with one or two groups selected from fluorine, chlorine,methyl, ethyl, trifluoromethyl, methxoy and trifluoromethoxy, with theproviso that if R³ and R⁴ together with the carbon atoms they areattached form a 5- to 6-membered heterocycle with a non-substitutednitrogen atom which is not directly attached to the pyrazole, then R⁷and R¹⁰ is different from hydrogen, with the proviso that if R⁷ and R¹⁰are hydrogen then the nitrogen atom of the 5- to 6-membered heterocycleformed by R³ and R⁴ together with the carbon atoms they are attached tois substituted with methyl, ethyl, methoxycarbonyl or ethoxycarbonyl, ora stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or a saltthereof, or a mixture of same.
 18. The method of claim 15, wherein: R¹is a group of the formula

wherein # is the point of attachment to the amino group, R⁵ is a groupselected from chlorine, methyl, ethyl, methoxy or cyclopropyl, whereinsaid methyl and ethyl are optionally substituted with methoxy oroptionally with up to three fluorine atoms, wherein said methoxy isoptionally substituted with up to three fluorine atoms, R⁶ is5-fluoropyridin-2-yl, 6-trifluoromethylpyridin-3-yl or cyclohexyl, or isa group of the formula

wherein ## is the point of attachment to the pyrazole ring, R³⁸ is ahydrogen atom or fluorine, R^(38a) is a hydrogen atom, R³⁹ is a hydrogenatom, R^(39a) is a hydrogen atom or cyano, R⁴⁰ is a hydrogen atom,fluorine, chlorine, cyano, methyl, difluoromethyl, trifluoromethyl,methoxy, ethoxy, difluoromethoxy, trifluoromethoxy, methoxycarbonyl orethoxycarbonyl, R⁷ is a hydrogen atom, methyl, ethyl, cyclopropylmethyl,2-cyclopropylethyl or 2,2-difluoroethyl, with the proviso that if R⁵ ismethoxy, difluoromethoxy or trifluoromethoxy then R⁷ is different fromhydrogen, with the proviso that if R⁶ is 5-fluoropyridin-2-yl or6-trifluoromethylpyridin-3-yl then R⁷ is different from hydrogen, R⁸ isa group selected from chlorine, methyl, ethyl, methoxy and cylcopropyl,R⁹ is pyridyl or4-cyanopentacyclo[4.2.0.0^(2,5).0^(3,8).0^(4,7)]octan-1-yl, or is agroup of the formula

wherein ## is the point of attachment to the pyrazole ring, R^(38b) is ahydrogen atom or fluorine, R^(38c) is a hydrogen atom, R^(39b) is ahydrogen atom, R^(39c) is a hydrogen atom, R^(40a) is a hydrogen atom,fluorine, chlorine, cyano, methyl, difluoromethyl, trifluoromethyl,methylamino, methoxy, difluoromethoxy, trifluoromethoxy or cyclopropyl,wherein said pyridyl is optionally substituted with fluorine, methyl,difluoromethyl, trifluoromethyl or methoxy, R¹⁰ is a hydrogen atom,methyl, ethyl, 2,2-difluoroethyl, cyclopropylmethyl, cyclobutylmethyl,2-cyclopropylethyl, 2-cyclopropyl-2-hydroxypropyl,2-cyclopropyl-2-hydroxyethyl, 2-methoxyethyl, or cyclopropyl, whereinsaid methyl and ethyl are optionally substituted with a group selectedfrom cyclopropyl, methoxy or optionally up to three fluorine atoms andis optionally additionally substituted with hydroxy, with the provisothat if R⁹ is pyridyl then R^(l)° is different from hydrogen, with theproviso that if R⁸ is methoxy then R^(l)° is different from hydrogen,R¹¹ is methyl, R¹² is a group of the formula

wherein ## is the point of attachment to the pyrazole ring, R^(38d) is ahydrogen atom, R^(38e) is a hydrogen atom, R^(39d) is a hydrogen atom,R^(39e) is a hydrogen atom, R^(40b) is fluorine or cyano, R¹³ is a groupselected from a hydrogen atom or methyl, R² is a hydrogen atom, methylor difluoromethyl, R³ is a group selected from a hydrogen atom,fluorine, chlorine, bromine, cyano, hydroxy, nitro, amino, ethylamino,dimethylamino, —O—C(═O)—NR³⁶R³⁷, —O—C(═O)—OR^(37a), —NH—C(═O)—OR^(37a),(C₁-C₄)-alkyl, methoxy, cyclopropyl, cyclobutyl, 4-membered heterocycle,1,3,4-oxadiazol-2-yl, 2-(trifluoromethyl)-1,3-dioxolan-2-yl,—(CH₂)_(q)—C(═O)—NR³⁴R³⁵, methoxycarbonyl and ethoxycarbonyl, whereinsaid (C₁-C₄)-alkyl is optionally substituted, identically ordifferently, with one or two groups selected from hydroxy, methoxy,methoxycarbonyl, ethoxycarbonyl, dimethylamino, a 4-memberedazaheterocycle and cyclopropyl and optionally up to three fluorineatoms, wherein said 4-membered azaheterocycle is optionally substitutedwith up to two fluorine atoms, wherein said methoxy is optionallysubstituted with cyano, cyclopropyl and optionally up to three fluorineatoms, wherein said cyclopropyl and cyclobutyl are optionallysubstituted with hydroxy, wherein said 4-membered heterocycle isoptionally substituted with hydroxy, wherein said 1,3,4-oxadiazol-2-ylis optionally substituted with methyl, wherein q is 0, R³⁴ is methyl,R³⁵ is methyl, or R³⁴ and R³⁵ together with the nitrogen atom they areattached form a 4- to 6-membered heterocycle ring wherein said 4- to6-membered heterocycle ring is optionally substituted, identically ordifferently, with one or two groups selected from a fluorine atom,methyl, difluoromethyl and trifluoromethyl, wherein R³⁶ is a methylatom, R³⁷ is a hydrogen atom or methyl, R^(37a) is methyl, with theproviso that if R³ is —(CH₂)_(q)C(═O)—NR³⁴R³⁵ O—C(═O)—NR³⁶R³⁷,—O—C(═O)—OR^(37a) or —NH—C(═O)—OR^(37a), then R⁷ and R¹⁰ are differentfrom hydrogen, with the proviso that if R³ is cyano then R² and R⁴ aredifferent from hydrogen, with the proviso that if R³ is cyano then R⁶and R⁹ are different from pyridyl, or R² and R³ together with the carbonatoms they are attached form a 5- to 6-membered carbocycle, apyrrolidinyl, a pyridyl or a phenyl ring, wherein said 5- to 6-memberedcarbocycle is optionally substituted, identically or differently, withone or two groups selected from oxo, methyl, trifluoromethyl andhydroxy, wherein said pyrrolidinyl is substituted with propyl ortert-butoxycarbonyl, R⁴ is a group selected from a hydrogen atom,methyl, 2-hydroxypropan-2-yl, fluoromethyl, difluoromethyl,methoxycarbonyl, ethoxycarbonyl and hydroxy, or R³ and R⁴ together withthe carbon atoms they are attached form a 5- to 6-membered carbocycle, apyrrolidinyl ring or a piperidinyl ring, a pyridyl group or a phenylring, wherein said pyrrolidinyl ring is substituted with propyl ortert-butoxycarbonyl, wherein said piperidinyl ring is substituted withpropyl or tert-butoxycarbonyl, wherein said 5- to 6-membered carbocycleis optionally substituted, identically or differently, with one or twogroups selected from oxo, hydroxy and methyl, or a stereoisomer, atautomer, an N-oxide, a hydrate, a solvate, or a salt thereof, or amixture of same.
 19. The method of claim 15, wherein the compound is

or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or asalt thereof, or a mixture of same.
 20. The method of claim 15, whereinthe compound is

or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or asalt thereof, or a mixture of same.
 21. The method of claim 15, whereinthe compound is

or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or asalt thereof, or a mixture of same.
 22. The method of claim 15, whereinthe compound is

or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or asalt thereof, or a mixture of same.
 23. The method of claim 15, whereinthe compound of formula (I), or a stereoisomer, a tautomer, an N-oxide,a hydrate, a solvate, or a salt thereof, or a mixture of same, isadministered as a pharmaceutical composition comprising the compound offormula (I), or a stereoisomer, a tautomer, an N-oxide, a hydrate, asolvate, or a salt thereof, or a mixture of same, in combination with aninert, non-toxic, pharmaceutically suitable auxiliary.
 24. The method ofclaim 15, wherein the compound of formula (I), or a stereoisomer, atautomer, an N-oxide, a hydrate, a solvate, or a salt thereof, or amixture of same, is administered as a pharmaceutical combinationcomprising the compound of formula (I), or a stereoisomer, a tautomer,an N-oxide, a hydrate, a solvate, or a salt thereof, or a mixture ofsame, in combination with a further active compound selected from thegroup consisting of the hypotensive active compounds, of theanti-inflammatory agents/immunosuppressive agents, the phosphatebinders, the sodium-phosphate co-transporters, NHE3 inhibitors,antiarrhythmic agents, agents that alter lipid metabolism and the activecompounds which modulate vitamin D metabolism.
 25. A method fortreatment of a cardiovascular or renal disorder in a patient in needthereof, comprising administering to said patient a compound of formula(I):

wherein R¹ is a group of the formula

wherein # is the point of attachment to the amino group, R⁵ is a groupselected from a halogen atom, cyano, (C₁-C₄)-alkyl, (C₁-C₄)-alkoxy,(C₃-C₆)-cycloalkyl, 4- to 6-membered heterocycle and(C₁-C₄)-alkylcarbonyl, wherein said (C₁-C₄)-alkyl is optionallysubstituted, identically or differently, with one or two groups selectedfrom —NR¹⁴R¹⁵, (C₁-C₄)-alkoxy and cyclopropyl and optionally up to fivefluorine atoms, wherein said cyclopropyl is optionally substituted withup to four fluorine atoms, wherein R¹⁴ is a hydrogen atom or(C₁-C₄)-alkyl, R¹⁵ is a hydrogen atom or (C₁-C₄)-alkyl, or R¹⁴ and R¹⁵together with the nitrogen atom they are attached form a 4- to5-membered heterocycle wherein said 4- to 5-membered heterocycle isoptionally substituted, identically or differently, with one, two orthree groups selected from (C₁-C₄)-alkyl trifluormethyl, difluoromethyland optionally up to five fluorine atoms, wherein said (C₁-C₄)-alkoxy isoptionally substituted with up to three fluorine atoms, wherein said 4-to 6-membered heterocycle is optionally substituted, identically ordifferently, with one or two groups selected from (C₁-C₄)-alkyl andoptionally up to five fluorine atoms, wherein said (C₃-C₆)-cycloalkyl isoptionally substituted, identically or differently, with one or twogroups selected from (C₁-C₄)-alkyl and optionally up to five fluorineatoms, R⁶ is 6-membered heteroaryl, 2-oxopyridin-1(2H)-yl, a 4- to8-membered heterocycle or (C₄-C₈)-cycloalkyl, or is a group of theformula

wherein ## is the point of attachment to the pyrazole ring, R³⁸ is ahydrogen atom, halogen or methyl, R^(38a) is a hydrogen atom, halogen ormethyl, R³⁹ is a hydrogen atom, cyano, fluorine or(C₁-C₄)-alkylsulfanyl, R^(39a) is a hydrogen atom, cyano, fluorine or(C₁-C₄)-alkylsulfanyl, R⁴⁰ is a hydrogen atom, halogen, cyano, hydroxy,—(CH₂)_(n)NR¹⁶R¹⁷, (C₁-C₄)-alkyl, (C₁-C₄)-alkoxy or(C₁-C₄)-alkoxycarbonyl, wherein said (C₁-C₄)-alkyl is optionallysubstituted with cyano and optionally with up to five fluorine atoms,wherein said (C₁-C₄)-alkoxy is optionally substituted with up to fivefluorine atoms, wherein n is 0 or 1, R¹⁶ is a hydrogen atom or(C₁-C₄)-alkyl, wherein said (C₁-C₄)-alkyl is optionally substituted withup to five fluorine atoms, R¹⁷ is a hydrogen atom or (C₁-C₄)-alkyl,wherein said (C₁-C₄)-alkyl is optionally substituted with up to fivefluorine atoms, or R¹⁶ and R¹⁷ together with the nitrogen atom they areattached form a 4- to 8-membered heterocycle wherein said 4- to8-membered heterocycle is optionally substituted, identically ordifferently, with one, two or three groups selected from (C₁-C₄)-alkyland optionally up to five fluorine atoms, wherein said 6-memberedheteroaryl group is optionally substituted, identically or differently,with one or two groups selected from a halogen atom, cyano,(C₁-C₄)-alkyl, and (C₁-C₄)-alkoxy, wherein said (C₁-C₄)-alkyl isoptionally substituted with up to five fluorine atoms, wherein said(C₁-C₄)-alkoxy is optionally substituted with up to three fluorineatoms, wherein said 2-oxopyridin-1(2H)-yl is optionally substituted,identically or differently, with one or two groups selected from ahalogen atom, cyano, (C₁-C₄)-alkyl and (C₁-C₄)-alkoxy, wherein said(C₁-C₄)-alkyl is optionally substituted with up to five luorine atoms,wherein said (C₁-C₄)-alkoxy is optionally substituted with up to threefluorine atoms, wherein said 4- to 8-membered heterocycle is optionallysubstituted, identically or differently, with one, two or three groupsselected from (C₁-C₄)-alkyl, cyano, (C₁-C₄)-alkoxycarbonyl andoptionally up to five fluorine atoms, wherein said (C₁-C₄)-alkyl isoptionally substituted with up to five fluorine atoms, wherein said(C₄-C₈)-cycloalkyl is optionally substituted, identically ordifferently, with one or two groups selected from (C₁-C₄)-alkyl, cyanoand optionally up to five fluorine atoms, wherein said (C₁-C₄)-alkyl isoptionally substituted with (C₃-C₆)-cycloalkyl and optionally up to fivefluorine atoms, R⁷ is a hydrogen atom, (C₁-C₄)-alkyl, a phenyl group, a5- to 6-membered heteroaryl group or (C₁-C₄)-alkylsulfonyl, wherein anyphenyl group and any 5- to 6-membered heteroaryl are each optionallysubstituted, identically or differently, with one, two or three groupsselected from a halogen atom, (C₁-C₄)-alkyl, trifluoromethyl,(C₁-C₄)-alkoxy and trifluoromethoxy, wherein said (C₁-C₄)-alkyl isoptionally substituted with a group selected from (C₃-C₆)-cycloalkyl, 4-to 6-membered heterocycle, hydroxy, —NR²⁰R²¹, (C₁-C₄)-alkoxy orbenzyloxy and optionally with up to five fluorine atoms, wherein said(C₃-C₆)-cycloalkyl is optionally substituted, identically ordifferently, with one or two groups selected from (C₁-C₄)-alkyl, hydroxyand up to five fluorine atoms, wherein said 4- to 6-membered heterocycleis optionally substituted, identically or differently, with one or twogroups selected from (C₁-C₄)-alkyl and optionally up to five fluorineatoms, and wherein R²⁰ is a hydrogen atom or (C₁-C₄)-alkyl, R²¹ is ahydrogen atom or (C₁-C₄)-alkyl, or R²⁰ and R²¹ together with thenitrogen atom they are attached form a 4- to 6-membered heterocyclewherein said 4- to 6-membered heterocycle is optionally substituted,identically or differently, with one, two or three groups selected from(C₁-C₄)-alkyl and optionally up to five fluorine atoms, with the provisothat if R⁵ is (C₁-C₄)-alkoxy then R⁷ is different from hydrogen, withthe proviso that if R⁶ is 6-membered heteroaryl then R⁷ is differentfrom hydrogen, with the proviso that if R⁶ is 2-oxopyridin-1(2H)-yl thenR⁷ is different from hydrogen, with the proviso that if R⁶ is a 4- to8-membered heterocycle then R⁷ is different from hydrogen, R⁸ is a groupselected from a halogen atom, cyano, (C₁-C₄)-alkyl, (C₁-C₄)-alkoxy,(C₃-C₆)-cycloalkyl, 4- to 6-membered heterocycle, (C₁-C₄)-alkylcarbonyland a phenyl group, wherein said (C₁-C₄)-alkyl is optionallysubstituted, identically or differently, with one or two groups selectedfrom —NR²²R²³ (C₁-C₄)-alkoxy and cyclopropyl and optionally up to fivefluorine atoms, wherein said cyclopropyl is optionally substituted withup to four fluorine atoms, wherein said (C₁-C₄)-alkoxy is optionallysubstituted with up to five fluorine atoms, wherein R²² is a hydrogenatom or (C₁-C₄)-alkyl, R²³ is a hydrogen atom or (C₁-C₄)-alkyl, or R²²and R²³ together with the nitrogen atom they are attached form a 4- to6-membered heterocycle wherein said 4- to 6-membered heterocycle isoptionally substituted, identically or differently, with one, two orthree groups selected from (C₁-C₄)-alkyl and optionally up to fivefluorine atoms, wherein said (C₁-C₄)-alkoxy is optionally substitutedwith up to five fluorine atoms, wherein said (C₃-C₆)-cycloalkyl isoptionally substituted, identically or differently, with one or twogroups selected from (C₁-C₄)-alkyl and optionally up to five fluorineatoms, wherein said 4- to 6-membered heterocycle is optionallysubstituted, identically or differently, with one or two groups selectedfrom (C₁-C₄)-alkyl and optionally up to five fluorine atoms, and whereinsaid phenyl group is optionally substituted, identically or differently,with one, two or three groups selected from a halogen atom, cyano,(C₁-C₄)-alkyl, trifluoromethyl, (C₁-C₄)-alkoxy and trifluoromethoxy, R⁹is 6-membered heteroaryl, 2-oxopyridin-1(2H)-yl, (C₃-C₈)-cycloalkyl, a4- to 8-membered heterocycle or (C₁-C₄)-alkyl, or is a group of theformula

wherein ## is the point of attachment to the pyrazole ring, R^(38b) is ahydrogen atom, halogen or methyl, R^(38c) is a hydrogen atom, halogen ormethyl, R^(39b) is a hydrogen atom, cyano, fluorine or(C₁-C₄)-alkylsulfanyl, R^(39c) is a hydrogen atom, cyano, fluorine or(C₁-C₄)-alkylsulfanyl, R^(40a) is a hydrogen atom, halogen, cyano,hydroxy, —(CH₂)_(n)NR^(16a)R^(17a), (C₁-C₄)-alkyl, (C₁-C₄)-alkoxy,(C₁-C₄)-alkoxycarbonyl, a 4- to 6-membered heterocycle, cyclopropyl orcyclobutyl, wherein said (C₁-C₄)-alkyl is optionally substituted withcyano and optionally with up to five fluorine atoms, wherein said(C₁-C₄)-alkoxy is optionally substituted with up to five fluorine atoms,wherein said 4- to 6-membered heterocycle is optionally substituted,identically or differently, with one, two or three groups selected from(C₁-C₄)-alkyl and optionally up to five fluorine atoms, wherein n is 0or 1, R^(16a) is a hydrogen atom or (C₁-C₄)-alkyl, wherein said(C₁-C₄)-alkyl is optionally substituted with up to five fluorine atoms,R^(17a) is a hydrogen atom or (C₁-C₄)-alkyl, wherein said (C₁-C₄)-alkylis optionally substituted with up to five fluorine atoms, or R^(16a) andR^(i7a) together with the nitrogen atom they are attached form a 4- to8-membered heterocycle wherein said 4- to 8-membered heterocycle isoptionally substituted, identically or differently, with one, two orthree groups selected from (C₁-C₄)-alkyl and optionally up to fivefluorine atoms, wherein said (C₁-C₄)-alkyl is optionally substitutedwith up to five fluorine atoms, wherein said 6-membered heteroaryl groupis optionally substituted, identically or differently, with one or twogroups selected from a halogen atom, cyano, (C₁-C₄)-alkyl, and(C₁-C₄)-alkoxy, wherein said (C₁-C₄)-alkyl is optionally substitutedwith up to five fluorine atoms, wherein said (C₁-C₄)-alkoxy isoptionally substituted with up to three fluorine atoms, wherein said2-oxopyridin-1(2H)-yl is optionally substituted, identically ordifferently, with one or two groups selected from a halogen atom, cyano,(C₁-C₄)-alkyl, and (C₁-C₄)-alkoxy, wherein said (C₁-C₄)-alkyl isoptionally substituted with up to five fluorine atoms, wherein said(C₁-C₄)-alkoxy is optionally substituted with up to three fluorineatoms, wherein said (C₃-C₈)-cycloalkyl is optionally substituted,identically or differently, with one or two groups selected from(C₁-C₄)-alkyl, cyano and optionally up to five fluorine atoms, whereinsaid (C₁-C₄)-alkyl is optionally substituted with (C₃-C₆)-cycloalkyl andoptionally up to five fluorine atoms, wherein said 4- to 8-memberedheterocycle is optionally substituted identically or differently, withone or two groups selected from (C₁-C₄)-alkyl, cyano,(C₁-C₄)-alkoxycarbonyl and optionally up to five fluorine atoms, whereinsaid (C₁-C₄)-alkyl is optionally substituted with up to five fluorineatoms, R¹⁰ is a hydrogen atom, (C₁-C₄)-alkyl, (C₃-C₅)-cycloalkyl,(C₁-C₄)-alkoxycarbonyl, mono-(C₁-C₄)-alkylamino, a phenyl group or a 5-to 6-membered heteroaryl group, wherein any phenyl group and any 5- to6-membered heteroaryl are each optionally substituted, identically ordifferently, with one, two or three groups selected from a halogen atom,(C₁-C₄)-alkyl, trifluoromethyl, (C₁-C₄)-alkoxy and trifluoromethoxy,wherein said (C₁-C₄)-alkyl is optionally substituted with a groupselected from (C₃-C₆)-cycloalkyl, 5-membered heteroaryl, —NR²⁸R²⁹,(C₁-C₄)-alkoxy or benzyloxy and optionally with up to five fluorineatoms and is optionally additionally substituted with hydroxy, whereinsaid (C₃-C₆)-cycloalkyl is optionally substituted, identically ordifferently, with hydroxy or one or two groups (C₁-C₄)-alkyl andoptionally up to five fluorine atoms, and wherein R²⁸ is a hydrogen atomor (C₁-C₄)-alkyl, R²⁹ is a hydrogen atom or (C₁-C₄)-alkyl, or R²⁸ andR²⁹ together with the nitrogen atom they are attached form a 4- to6-membered heterocycle wherein said 4- to 6-membered heterocycle isoptionally substituted, identically or differently, with one, two orthree groups selected from (C₁-C₄)-alkyl and optionally up to fivefluorine atoms, wherein said 5-membered heteroaryl is optionallysubstituted with (C₁-C₄)-alkyl, with the proviso that if R⁹ is6-membered heterorayl then R¹⁰ is different from hydrogen, with theproviso that if R⁹ is 2-oxopyridin-1(2H)-yl then R¹⁰ is different fromhydrogen, with the proviso that if R⁹ is a 4- to 8-membered heterocyclethen R¹⁰ is different from hydrogen, with the proviso that if R⁸ is(C₁-C₄)-alkoxy then R¹⁰ is different from hydrogen, R¹¹ is a groupselected from a hydrogen atom, a fluorine atom, a chlorine atom,(C₁-C₄)-alkyl and cyclopropyl, wherein said (C₁-C₄)-alkyl is optionallysubstituted with cyclopropyl and optionally up to five fluorine atoms,R¹² is a 6-membered heteroaryl group, 2-oxopyridin-1(2H)-yl,(C₄-C₈)-cycloalkyl or (C₁-C₄)-alkyl, or is a group of the formula

wherein ## is the point of attachment to the pyrazole ring, R^(38d) is ahydrogen atom, halogen or methyl, R^(38e) is a hydrogen atom, halogen ormethyl, R^(39d) is a hydrogen atom, cyano, fluorine or(C₁-C₄)-alkylsulfanyl, R^(39e) is a hydrogen atom, cyano, fluorine or(C₁-C₄)-alkylsulfanyl, R^(40b) is a hydrogen atom, halogen, cyano,hydroxy, —(CH₂)_(n)NR^(16a)R^(17a), (C₁-C₄)-alkyl, (C₁-C₄)-alkoxy,(C₁-C₄)-alkoxycarbonyl, a 4- to 6-membered heterocycle, cyclopropyl orcyclobutyl, wherein said (C₁-C₄)-alkyl is optionally substituted withcyano and optionally with up to five fluorine atoms, wherein said(C₁-C₄)-alkoxy is optionally substituted with up to five fluorine atoms,wherein said 4- to 6-membered heterocycle is optionally substituted,identically or differently, with one, two or three groups selected from(C₁-C₄)-alkyl and optionally up to five fluorine atoms, wherein n is 0or 1, R^(16a) is a hydrogen atom or (C₁-C₄)-alkyl, wherein said(C₁-C₄)-alkyl is optionally substituted with up to five fluorine atoms,R^(17a) is a hydrogen atom or (C₁-C₄)-alkyl, wherein said (C₁-C₄)-alkylis optionally substituted with up to five fluorine atoms, or R^(16a) andR^(17a) together with the nitrogen atom they are attached form a 4- to8-membered heterocycle wherein said 4- to 8-membered heterocycle isoptionally substituted, identically or differently, with one, two orthree groups selected from (C₁-C₄)-alkyl and optionally up to fivefluorine atoms, wherein said 6-membered heteroaryl group is optionallysubstituted, identically or differently, with one or two groups selectedfrom a halogen atom, cyano, (C₁-C₄)-alkyl, and (C₁-C₄)-alkoxy, whereinsaid (C₁-C₄)-alkyl is optionally substituted with up to five fluorineatoms, wherein said (C₁-C₄)-alkoxy is optionally substituted with up tothree fluorine atoms, wherein said 2-oxopyridin-1(2H)-yl is optionallysubstituted, identically or differently, with one or two groups selectedfrom a halogen atom, cyano, (C₁-C₄)-alkyl, and (C₁-C₄)-alkoxy, whereinsaid (C₁-C₄)-alkyl is optionally substituted with up to five fluorineatoms, wherein said (C₁-C₄)-alkoxy is optionally substituted with up tothree fluorine atoms, wherein said (C₄-C₈)-cycloalkyl is optionallysubstituted, identically or differently, with one or two groups selectedfrom (C₁-C₄)-alkyl or cyano and optionally up to five fluorine atoms,R¹³ is a group selected from a hydrogen atom, a fluorine atom, achlorine atom, (C₁-C₄)-alkyl and cyclopropyl, wherein said (C₁-C₄)-alkylis optionally substituted with cyclopropyl and up to five fluorineatoms, R² is a group selected from a hydrogen atom, (C₁-C₄)-alkyl,(C₃-C₆)-cycloalkyl and (C₁-C₄)-alkoxycarbonyl, wherein said(C₁-C₄)-alkyl is optionally substituted, identically or differently,with one or two groups selected from hydroxy, (C₁-C₄)-alkoxy,cyclopropyl and optionally up to five fluorine atoms, R³ is a groupselected from a hydrogen atom, a halogen atom, cyano, hydroxy, nitro,amino, mono-(C₁-C₄)-alkylamino, di-(C₁-C₄)-alkylamino,(C₁-C₄)-alkylsulfanyl, (C₁-C₄)-alkylsulfinyl, (C₁-C₄)-alkylsulfonyl,(C₁-C₆)-alkyl, (C₁-C₄)-alkoxy, (C₃-C₆)-cycloalkyl, 4- to 6-memberedheterocycle, 5- to 6-membered heteroaryl, —(CH₂)_(q)C(═O)—NR³⁴R³⁵,—O—C(═O)—NR³⁶R³⁷, —O—C(═O)—OR^(37a), —NH—C(═O)—NR³⁶R³⁷,—N(CH₃)—C(═O)—NR³⁶R³⁷, —NH—C(═O)—OR^(37a),—N(CH₃)—C(═O)—OR^(37a)—NH—C(═O)—R³⁷, —N(CH₃)—C(═O)—R³⁷,(C₁-C₄)-alkylcarbonyl, (C₁-C₄)-alkylcarbonyloxy and(C₁-C₄)-alkoxycarbonyl, wherein said (C₁-C₆)-alkyl is optionallysubstituted, identically or differently, with one or two groups selectedfrom hydroxy, amino, mono-(C₁-C₄)-alkylamino, di-(C₁-C₄)-alkylamino,cyano, (C₁-C₄)-alkoxy, 4- to 6-membered heterocycle,(C₁-C₄)-alkoxycarbonyl and cyclopropyl and optionally up to six fluorineatoms, wherein said 4- to 6-membered heterocycle is optionallysubstituted with (C₁-C₄)-alkyl or cyclopropyl and optionally up to twofluorine atoms, wherein said (C₁-C₄)-alkoxy is optionally substitutedwith cyano, cyclopropyl and optionally up to five fluorine atoms,wherein said (C₁-C₄)-alkyl of mono-(C₁-C₄)-alkylamino is optionallysubstituted with cyano, cyclopropyl and optionally up to five fluorineatoms, wherein said di-(C₁-C₄)-alkylamino is optionally substituted withcyano, cyclopropyl and optionally up to five fluorine atoms, whereinsaid (C₃-C₆)-cycloalkyl is optionally substituted, identically ordifferently, with one or two groups selected from (C₁-C₄)-alkyl,(C₁-C₄)-alkoxy, hydroxy and cyclopropyl and optionally up to fivefluorine atoms, wherein said 4- to 6-membered heterocycle is optionallysubstituted, identically or differently, with one or two groups selectedfrom (C₁-C₄)-alkyl, trifluoromethyl, difluoromethyl, (C₁-C₄)-alkoxy,(C₁-C₄)-alkoxycarbonyl, mono-(C₁-C₄)-alkylaminocarbonyl,di-(C₁-C₄)-alkylaminocarbonyl, (C₁-C₄)-alkylcarbonyl, hydroxy andcyclopropyl and optionally up to five fluorine atoms, wherein said 5- to6-membered heteroaryl is optionally substituted, identically ordifferently, with one or two groups selected from (C₁-C₄)-alkyl,(C₁-C₄)-alkoxy, and cyclopropyl and optionally up to five fluorineatoms, wherein q is 0 or 1, R³⁴ is a hydrogen atom or (C₁-C₄)-alkyl, R³⁵is a hydrogen atom, (C₁-C₄)-alkyl or phenyl, or R³⁴ and R³⁵ togetherwith the nitrogen atom they are attached form a 4- to 7-memberedheterocyclyl ring wherein said 4- to 7-membered heterocyclyl ring isoptionally substituted, identically or differently, with one, two orthree groups selected from a fluorine atom, hydroxy, (C₁-C₄)-alkyl,(C₁-C₄)-alkoxy, cyclopropyl, difluoromethyl, trifluoromethyl andtrifluoromethoxy, wherein R³⁶ is a hydrogen atom or methyl, R³⁷ is ahydrogen atom, methyl, difluoromethyl, trifluoromethyl or cyclopropyl,R^(37a) is methyl, difluoromethyl, trifluoromethyl or cyclopropyl, withthe proviso that if R³ is —(CH₂)_(q)C(═O)—NR³⁴R³⁵, —O—C(═O)—NR³⁶R³⁷,—O—C(═O)—OR^(37a), —N(CH₃)—C(═O)—NR³⁶R³⁷, —NH—C(═O)—OR^(37a),—NH—C(═O)—NR³⁶R³⁷, —N(CH₃)—C(═O)—OR^(37a)—NH—C(═O)—R³⁷ or—N(CH₃)—C(═O)—R³⁷, then R⁷ and R¹⁰ are different from hydrogen, with theproviso that if R³ is cyano then R² and R⁴ are different from hydrogen,with the proviso that if R³ is cyano then R⁶ and R⁹ are different from6-membered heteroaryl, or R² and R³ together with the carbon atoms theyare attached form a 4- to 6-membered carbocycle, a 4- to 7-memberedazaheterocycle, a 4- to 7-membered oxaheterocycle, a 5- to 6-memberedheteroaryl group or a phenyl ring, wherein said 4- to 7-memberedazaheterocycle is optionally substituted, identically or differently,with one or two groups selected from hydroxy, oxo, (C₁-C₄)-alkyl,trifluoromethyl, (C₁-C₄)-alkylcarbonyl and (C₁-C₄)-alkoxycarbonyl andoptionally up to five fluorine atoms, wherein said 4- to 7-memberedoxaheterocycle is optionally substituted, identically or differently,with one or two groups selected from hydroxy, oxo, (C₁-C₄)-alkyl,trifluoromethyl, (C₁-C₄)-alkylcarbonyl and (C₁-C₄)-alkoxycarbonyl andoptionally up to five fluorine atoms, wherein said 4- to 6-memberedcarbocycle is optionally substituted, identically or differently, withone or two groups selected from hydroxy, oxo, amino,mono-(C₁-C₄)-alkylamino, di-(C₁-C₄)-alkylamino, (C₁-C₄)-alkyl,trifluoromethyl, (C₁-C₄)-alkylcarbonyl and (C₁-C₄)-alkoxycarbonyl andoptionally up to five fluorine atoms, and wherein any phenyl group andany 5- to 6-membered heteroaryl group are each optionally substituted,identically or differently, with one, two or three groups selected froma halogen atom, (C₁-C₄)-alkyl, trifluoromethyl, (C₁-C₄)-alkoxy andtrifluoromethoxy, with the proviso that if R² and R³ together with thecarbon atoms they are attached to form a 4- to 7-membered azaheterocyclewith a non-substituted nitrogen atom which is not directly attached tothe pyrazole, then R⁷ and R¹⁰ are different from hydrogen, with theproviso that if R⁷ and R¹⁰ are hydrogen then the nitrogen atom of the 4-to 7-membered azaheterocycle formed by R² and R³ together with thecarbon atoms they are attached to is substituted with (C₁-C₄)-alkyl or(C₁-C₄)-alkoxycarbonyl, R⁴ is a group selected from a hydrogen atom,(C₁-C₄)-alkyl, (C₃-C₆)-cycloalkyl and (C₁-C₄)-alkoxycarbonyl andhydroxy, wherein said (C₁-C₄)-alkyl is optionally substituted,identically or differently, with one or two groups selected fromhydroxy, (C₁-C₄)-alkoxy and cyclopropyl and optionally up to fivefluorine atoms, or R³ and R⁴ together with the carbon atoms they areattached form a 4- to 6-membered carbocycle, a 4- to 7-memberedheterocycle, a 5- to 6-membered heteroaryl group or a phenyl ring,wherein said 4- to 7-membered heterocycle is optionally substituted,identically or differently, with one or two groups selected from afluorine atom, hydroxy, oxo, (C₁-C₄)-alkyl, trifluoromethyl,(C₁-C₄)-alkylcarbonyl and (C₁-C₄)-alkoxycarbonyl and optionally up tofive fluorine atoms, wherein said 4- to 6-membered carbocycle isoptionally substituted, identically or differently, with one or twogroups selected from a fluorine atom, hydroxy, oxo, (C₁-C₄)-alkyl,trifluoromethyl, (C₁-C₄)-alkylcarbonyl and (C₁-C₄)-alkoxycarbonyl andoptionally up to five fluorine atoms, and wherein any phenyl group andany 5- to 6-membered heteroaryl group are each optionally substituted,identically or differently, with one, two or three groups selected froma halogen atom, (C₁-C₄)-alkyl, trifluoromethyl, (C₁-C₄)-alkoxy andtrifluoromethoxy, with the proviso that if R³ and R⁴ together with thecarbon atoms they are attached form a 4- to 7-membered heterocycle witha non-substituted nitrogen atom which is not directly attached to thepyrazole, then R⁷ and R¹⁰ is different from hydrogen, with the provisothat if R⁷ and R¹⁰ are hydrogen then the nitrogen atom of the 4- to7-membered heterocycle formed by R³ and R⁴ together with the carbonatoms they are attached to is substituted with (C₁-C₄)-alkyl or(C₁-C₄)-alkoxycarbonyl, or a stereoisomer, a tautomer, an N-oxide, ahydrate, a solvate, or a salt thereof, or a mixture of same.
 26. Themethod of claim 25, wherein R¹ is a group of the formula

wherein # is the point of attachment to the amino group, R⁵ is a groupselected from fluorine, chlorine, cyano, (C₁-C₄)-alkyl, methoxy, ethoxy,(C₃-C₅)-cycloalkyl, methylcarbonyl and ethylcarbonyl, wherein said(C₁-C₄)-alkyl is optionally substituted, identically or differently,with one or two groups selected from —NR¹⁴R¹⁵, methoxy, ethoxy,difluoromethoxy, trifluoromethoxy and cyclopropyl and optionally up tofive fluorine atoms, wherein said cyclopropyl is optionally substitutedwith up to four fluorine atoms, wherein R¹⁴ is a hydrogen atom or(C₁-C₄)-alkyl, R¹⁵ is a hydrogen atom or (C₁-C₄)-alkyl, or R¹⁴ and R¹⁵together with the nitrogen atom they are attached form a 4- to5-membered heterocycle, wherein said 4- to 5-membered heterocycle isoptionally substituted, identically or differently, with one or twogroups selected from (C₁-C₄)-alkyl, trifluormethyl, difluoromethyl andoptionally up to five fluorine atoms, wherein said methoxy and ethoxyare optionally substituted with up to three fluorine atoms, wherein said(C₃-C₅)-cycloalkyl is optionally substituted with up to four fluorineatoms, R⁶ is pyridyl, pyrimidyl, 2-oxopyridin-1(2H)-yl,(C₅-C₈)-cycloalkyl or a 6- to 8-membered heterocycle or is a group ofthe formula

wherein ## is the point of attachment to the pyrazole ring, R³⁸ is ahydrogen atom, halogen or methyl, R^(38a) is a hydrogen atom, halogen ormethyl, R³⁹ is a hydrogen atom, cyano, fluorine or(C₁-C₄)-alkylsulfanyl, R^(39a) is a hydrogen atom, cyano, fluorine or(C₁-C₄)-alkylsulfanyl, R⁴⁰ is a hydrogen atom, fluorine, chlorine,cyano, hydroxy, —(CH₂)_(n)NR¹⁶R¹⁷, (C₁-C₃)-alkyl, (C₁-C₃)-alkoxy or(C₁-C₄)-alkoxycarbonyl, wherein said (C₁-C₃)-alkyl is optionallysubstituted with cyano and optionally with up to five fluorine atoms,wherein said (C₁-C₃)-alkoxy is optionally substituted with up to fivefluorine atoms, wherein n is 0 or 1, R¹⁶ is a hydrogen atom or(C₁-C₄)-alkyl, R¹⁷ is a hydrogen atom or (C₁-C₄)-alkyl, or R¹⁶ and R¹⁷together with the nitrogen atom they are attached form a 4- to6-membered heterocycle wherein said 4- to 6-membered heterocycle isoptionally substituted, identically or differently, with one, two orthree groups selected from (C₁-C₄)-alkyl and optionally up to fivefluorine atoms, wherein said pyridyl and pyrimidyl are optionallysubstituted, identically or differently, with one or two groups selectedfrom a halogen atom, cyano, methyl, ethyl, methoxy and ethoxy, whereinsaid (C₁-C₄)-alkyl is optionally substituted with up to five fluorineatoms, wherein said methoxy and ethoxy are optionally substituted withup to three fluorine atoms, wherein said 2-oxopyridin-1(2H)-yl isoptionally substituted, identically or differently, with one or twogroups selected from fluorine, cyano, methyl, ethyl, methoxy and ethoxy,wherein said methyl and ethyl are optionally substituted with up tothree fluorine atoms, wherein said methoxy and ethoxy are optionallysubstituted with up to three fluorine atoms, wherein said 6- to8-membered heterocycle is optionally substituted, identically ordifferently, with one or two groups selected from (C₁-C₄)-alkyl, cyano,(C₁-C₄)-alkoxycarbonyl and optionally up to five fluorine atoms, whereinsaid (C₁-C₄)-alkyl is optionally substituted with up to three fluorineatoms, wherein said (C₅-C₈)-cycloalkyl is optionally substituted,identically or differently, with one or two groups selected from(C₁-C₄)-alkyl and cyano, and optionally up to five fluorine atoms,wherein said (C₁-C₄)-alkyl is optionally substituted with up to threefluorine atoms, R⁷ is a hydrogen atom, (C₁-C₄)-alkyl, methylsulfonyl orethylsulfonyl, wherein said (C₁-C₄)-alkyl is optionally substituted witha group selected from (C₃-C₆)-cycloalkyl, hydroxy, —NR²⁰R²¹, methoxy,ethoxy or benzyloxy and optionally with up to five fluorine atoms,wherein said (C₃-C₆)-cycloalkyl is optionally substituted with hydroxyand optionally up to four fluorine atoms, and wherein R²⁰ is a hydrogenatom or (C₁-C₄)-alkyl, R²¹ is a hydrogen atom or (C₁-C₄)-alkyl, with theproviso that if R⁵ is methoxy or ethoxy then R⁷ is different fromhydrogen, with the proviso that if R⁶ is pyridyl or pyrimidyl then R⁷ isdifferent from hydrogen, with the proviso that if R⁶ is2-oxopyridin-1(2H)-yl then R⁷ is different from hydrogen, with theproviso that if R⁶ is a 6- to 8-membered heterocycle then le isdifferent from hydrogen, R⁸ is a group selected from fluorine, chlorine,cyano, (C₁-C₄)-alkyl, methoxy, ethoxy, methylcarbonyl, ethylcarbonyl and(C₃-C₅)-cycloalkyl, wherein said (C₁-C₄)-alkyl is optionally substitutedwith methoxy, —NR²²R²³ and cyclopropyl and optionally up to fivefluorine atoms, wherein said cyclopropyl is optionally substituted withup to four fluorine atoms, wherein said methoxy is optionallysubstituted with up to three fluorine atoms, wherein R²² is a hydrogenatom or (C₁-C₄)-alkyl, R²³ is a hydrogen atom or (C₁-C₄)-alkyl, or R²²and R²³ together with the nitrogen atom they are attached form a 4- to6-membered heterocycle wherein said 4- to 6-membered heterocycle isoptionally substituted, identically or differently, with one, two orthree groups selected from (C₁-C₄)-alkyl and optionally up to fivefluorine atoms, wherein said methoxy and ethoxy are optionallysubstituted with up to three fluorine atoms, and wherein said(C₃-C₅)-cycloalkyl is optionally substituted with up to four fluorineatoms, R⁹ is pyridyl, pyrimidyl, 2-oxopyridin-1(2H)-yl,(C₅-C₈)-cycloalkyl or a 6- to 8-membered heterocycle or (C₁-C₄)-alkyl,or is a group of the formula

wherein ## is the point of attachment to the pyrazole ring, R^(38b) is ahydrogen atom, halogen or methyl, R^(38c) is a hydrogen atom, halogen ormethyl, R^(39b) is a hydrogen atom, cyano, fluorine or(C₁-C₄)-alkylsulfanyl, R^(39c) is a hydrogen atom, cyano, fluorine or(C₁-C₄)-alkylsulfanyl, R^(40a) is a hydrogen atom, fluorine, chlorine,cyano, hydroxy, —(CH₂)_(n)NR^(16a)R^(17a), (C₁-C₃)-alkyl,(C₁-C₃)-alkoxy, (C₁-C₄)-alkoxycarbonyl, a 4- to 6-membered heterocycle,cyclopropyl or cyclobutyl, wherein said (C₁-C₃)-alkyl is optionallysubstituted with cyano and optionally with up to five fluorine atoms,wherein said (C₁-C₃)-alkoxy is optionally substituted with up to fivefluorine atoms, wherein said 4- to 6-membered heterocycle is optionallysubstituted, identically or differently, with one, two or three groupsselected from (C₁-C₄)-alkyl and optionally up to five fluorine atoms,wherein n is 0 or 1, R^(16a) is a hydrogen atom or (C₁-C₄)-alkyl,R^(17a) is a hydrogen atom or (C₁-C₄)-alkyl, or R^(16a) and R^(17a)together with the nitrogen atom they are attached form a 4- to6-membered heterocycle wherein said 4- to 6-membered heterocycle isoptionally substituted, identically or differently, with one, two orthree groups selected from (C₁-C₄)-alkyl and optionally up to fivefluorine atoms, wherein said (C₁-C₄)-alkyl is optionally substitutedwith up to five fluorine atoms, wherein said pyridyl and pyrimidyl areoptionally substituted, identically or differently, with one or twogroups selected from a halogen atom, cyano, methyl, ethyl, methoxy andethoxy, wherein said methyl and ethyl is optionally substituted with upto three fluorine atoms, wherein said methoxy and ethoxy are optionallysubstituted with up to three fluorine atoms, wherein said2-oxopyridin-1(2H)-yl is optionally substituted, identically ordifferently, with one or two groups selected from fluorine, cyano,methyl, ethyl, methoxy and ethoxy, wherein said methyl and ethyl areoptionally substituted with up to three fluorine atoms, wherein saidmethoxy and ethoxy are optionally substituted with up to three fluorineatoms, wherein said 6- to 8-membered heterocycle is optionallysubstituted, identically or differently, with one or two groups selectedfrom methyl, ethyl, cyano and (C₁-C₄)-alkoxycarbonyl and optionally upto five fluorine atoms, wherein said methyl is optionally substitutedwith up to three fluorine atoms, wherein said (C₅-C₈)-cycloalkyl isoptionally substituted, identically or differently, with one or twogroups selected from methyl, ethyl and cyano, and optionally up to fivefluorine atoms, wherein said methyl is optionally substituted with up tothree fluorine atoms, R¹⁰ is a hydrogen atom, (C₁-C₄)-alkyl or(C₃-C₅)-cycloalkyl, wherein said (C₁-C₄)-alkyl is optionally substitutedwith a group selected from (C₃-C₆)-cycloalkyl,2-methyl-2H-tetrazol-5-yl, 1-methyl-1H-tetrazol-5-yl, —NR²⁸R²⁹, methoxy,ethoxy or benzyloxy and optionally with up to five fluorine atomsoptionally with up to five fluorine atoms and is optionally additionallysubstituted with hydroxy, wherein said (C₃-C₆)-cycloalkyl is optionallysubstituted with up to four fluorine atoms, and wherein R²⁸ is ahydrogen atom or (C₁-C₄)-alkyl, R²⁹ is a hydrogen atom or (C₁-C₄)-alkyl,with the proviso that if R⁹ is pyridyl or pyrimidyl then R¹⁰ isdifferent from hydrogen, with the proviso that if R⁹ is2-oxopyridin-1(2H)-yl then R¹⁰ is different from hydrogen, with theproviso that if R⁹ is a 6- to 8-membered heterocycle then R¹⁰ isdifferent from hydrogen, with the proviso that if R⁸ is methoxy orethoxy then R¹⁰ is different from hydrogen, R¹¹ is a group selected froma hydrogen atom, (C₁-C₄)-alkyl and cyclopropyl, wherein said(C₁-C₄)-alkyl is optionally substituted with cyclopropyl and optionallywith up to five fluorine atoms, R¹² is pyridyl or 2-oxopyridin-1(2H)-yl,or is a group of the formula

wherein ## is the point of attachment to the pyrazole ring, R^(38d) is ahydrogen atom, fluorine or methyl, R^(38e) is a hydrogen atom, fluorineor methyl, R^(39d) is a hydrogen atom, cyano or fluorine, R^(39e) is ahydrogen atom, R^(40b) is a hydrogen atom, fluorine, chlorine, cyano,hydroxy, methyl, trifluoromethyl, methoxy, trifluoromethoxy ormethoxycarbonyl, wherein said pyridyl is optionally substituted,identically or differently, with one or two groups selected fromfluorine, cyano, methyl and methoxy, wherein said methyl is optionallysubstituted with up to three fluorine atoms, wherein said methoxy isoptionally substituted with up to three fluorine atoms, wherein said2-oxopyridin-1(2H)-yl is optionally substituted, identically ordifferently, with one or two groups selected from fluorine, cyano,methyl and methoxy, wherein said methyl is optionally substituted withup to three fluorine atoms, wherein said methoxy is optionallysubstituted with up to three fluorine atoms, R¹³ is a group selectedfrom a hydrogen atom, (C₁-C₄)-alkyl and cyclopropyl, wherein said(C₁-C₄)-alkyl is optionally substituted with cyclopropyl and optionallywith up to five fluorine atoms, R² is a group selected from a hydrogenatom, (C₁-C₄)-alkyl, cyclopropyl, methoxycarbonyl and ethoxycarbonyl,wherein said (C₁-C₄)-alkyl is optionally substituted, identically ordifferently, with one or two groups selected from hydroxy, methoxy,ethoxy, cyclopropyl and optionally up to five fluorine atoms, R³ is agroup selected from a hydrogen atom, fluorine, chlorine, bromine, cyano,hydroxy, nitro, amino, mono-(C₁-C₄)-alkylamino, di-(C₁-C₄)-alkylamino,(C₁-C₄)-alkylsulfanyl, (C₁-C₄)-alkylsulfinyl, (C₁-C₄)-alkylsulfonyl,(C₁-C₆)-alkyl, (C₁-C₄)-alkoxy, —O'C(═O)—NR³⁶R³⁷, —O—C(═O)—OR^(37a),—NH—C(═O)—NR³⁶R³⁷, —N(CH₃)—C(═O)—NR³⁶R³⁷, —NH—C(═O)—OR^(37a),—N(CH₃)—C(═O)—OR^(37a)—NH—C(═O)—R³⁷, —N(CH₃)—C(═O)—R³⁷,(C₃-C₅)-cycloalkyl, 4- to 6-membered heterocycle, 5- to 6-memberedheteroaryl, —(CH₂)_(q)—C(═O)—NR³⁴R³⁵, methylcarbonyl, ethylcarbonyl,(C₁-C₄)-alkylcarbonyloxy and (C₁-C₄)-alkoxycarbonyl, wherein said(C₁-C₆)-alkyl is optionally substituted, identically or differently,with one or two groups selected from hydroxy, amino,mono-(C₁-C₄)-alkylamino, di-(C₁-C₄)-alkylamino, cyano, methoxy, ethoxy,methoxycarbonyl, ethoxycarbony, 4- to 6-membered heterocycle, 1 andcyclopropyl and optionally up to five fluorine atoms, wherein said 4- to6-membered heterocycle is optionally substituted with methyl, ethyl orcyclopropyl and optionally up to two fluorine atoms, wherein said(C₁-C₄)-alkoxy is optionally substituted with cyano, cyclopropyl andoptionally up to five fluorine atoms, wherein said (C₃-C₅)-cycloalkyl isoptionally substituted with hydroxyl, methoxy, ethoxy and optionally upto four fluorine atoms, wherein said 4- to 6-membered heterocycle isoptionally substituted with hydroxyl, trifluoromethyl, methoxy, ethoxyand optionally up to four fluorine atoms, wherein said 5- to 6-memberedheteroaryl is optionally substituted, identically or differently, withone or two groups selected from methyl, ethyl and methoxy and optionallyup to four fluorine atoms, wherein q is 0, R³⁴ is a hydrogen atom or(C₁-C₄)-alkyl, R³⁵ is a hydrogen atom or (C₁-C₄)-alkyl, or R³⁴ and R³⁵together with the nitrogen atom they are attached form a 4- to7-membered heterocycle, wherein said 4- to 7-membered heterocyclel ringis optionally substituted, identically or differently, with one, two orthree groups selected from a fluorine atom, hydroxy, methyl, ethyl,methoxy, ethoxy, cyclopropyl, difluoromethyl, trifluoromethyl andtrifluoromethoxy, wherein R³⁶ is a hydrogen atom or methyl, R³⁷ is ahydrogen atom, methyl, difluoromethyl, trifluoromethyl or cyclopropyl,R^(37a) is methyl, difluoromethyl, trifluoromethyl or cyclopropyl, withthe proviso that if R³ is —(CH₂)_(q)C(═O)—NR³⁴R³⁵, —O—C(═O)—NR³⁶R³⁷,—O—C(═O)—OR^(37a), —N(CH₃)—C(═O)—NR³⁶R³⁷, —NH—C(═O)—OR^(37a),—NH—C(═O)—NR³⁶R³⁷, —N(CH₃)—C(═O)—OR^(37a), —NH—C(═O)—R³⁷ or—N(CH₃)—C(═O)—R³⁷, then R⁷ and R¹⁰ are different from hydrogen, with theproviso that if R³ is cyano then R² and R⁴ are different from hydrogen,with the proviso that if R³ is cyano then R⁶ and R⁹ are different from6-membered heteroaryl, or R² and R³ together with the carbon atoms theyare attached form a 5- to 6-membered carbocycle, a 5- to 7-memberedazaheterocycle, a 5- to 7-membered oxaheterocycle, a 5- to 6-memberedheteroaryl group or a phenyl ring, wherein said 5- to 7-memberedazaheterocycle is optionally substituted, identically or differently,with one or two groups selected from oxo, methyl, ethyl, propyl,trifluoromethyl and (C₁-C₄)-alkoxycarbonyl and optionally up to fourfluorine atoms, wherein said 5- to 7-membered oxaheterocycle isoptionally substituted, identically or differently, with one or twogroups selected from oxo, methyl, ethyl, trifluoromethyl and(C₁-C₄)-alkoxycarbonyl and optionally up to four fluorine atoms, whereinsaid 5- to 6-membered carbocycle is optionally substituted, identicallyor differently, with one or two groups selected from hydroxy, oxo,amino, mono-(C₁-C₄)-alkylamino, di-(C₁-C₄)-alkylamino, methyl, ethyl,trifluoromethyl and (C₁-C₄)-alkoxycarbonyl and optionally up to fourfluorine atoms, and wherein any phenyl group and any 5- to 6-memberedheteroaryl group are each optionally substituted, identically ordifferently, with one or two groups selected from fluorine, chlorine,methyl, ethyl, trifluoromethyl, methxoy and trifluoromethoxy, with theproviso that if R² and R³ together with the carbon atoms they areattached to form a 5- to 7-membered azaheterocycle with anon-substituted nitrogen atom which is not directly attached to thepyrazole, then R⁷ and R^(m) are different from hydrogen, with theproviso that if R⁷ and R¹⁰ are hydrogen then the nitrogen atom of the 5-to 7-membered azaheterocycle formed by R² and R³ together with thecarbon atoms they are attached to is substituted with methyl, ethyl or(C₁-C₄)-alkoxycarbonyl, R⁴ is a group selected from a hydrogen atom,(C₁-C₄)-alkyl, cyclopropyl, methoxycarbonyl, ethoxycarbonyl and hydroxy,wherein said (C₁-C₄)-alkyl is optionally substituted, identically ordifferently, with one or two groups selected from hydroxy, methoxy andcyclopropyl and optionally up to five fluorine atoms, or R³ and R⁴together with the carbon atoms they are attached form a 5- to 6-memberedcarbocycle, a 5- to 7-membered heterocycle, a 5- to 6-memberedheteroaryl group or a phenyl ring, wherein said 5- to 7-memberedheterocycle is optionally substituted, identically or differently, withone or two groups selected from oxo, methyl, ethyl, propyltrifluoromethyl and (C₁-C₄)-alkoxycarbonyl and optionally up to fourfluorine atoms, wherein said 5- to 6-membered carbocycle is optionallysubstituted, identically or differently, with one or two groups selectedfrom oxo, hydroxyl, methyl, ethyl, trifluoromethyl and(C₁-C₄)-alkoxycarbonyl and optionally up to four fluorine atoms, andwherein any phenyl group and any 5- to 6-membered heteroaryl group areeach optionally substituted, identically or differently, with one or twogroups selected from fluorine, chlorine, methyl, ethyl, trifluoromethyl,methoxy and trifluoromethoxy, with the proviso that if R³ and R⁴together with the carbon atoms they are attached form a 5- to 7-memberedheterocycle with a non-substituted nitrogen atom which is not directlyattached to the pyrazole, then R⁷ and R¹⁰ is different from hydrogen,with the proviso that if le and R¹⁰ are hydrogen then the nitrogen atomof the 5- to 7-membered heterocycle formed by R³ and R⁴ together withthe carbon atoms they are attached to is substituted with methyl, ethylor (C₁-C₄)-alkoxycarbonyl, or a stereoisomer, a tautomer, an N-oxide, ahydrate, a solvate, or a salt thereof, or a mixture of same.
 27. Themethod of claim 25, wherein: R¹ is a group of the formula

wherein # is the point of attachment to the amino group, R⁵ is a groupselected from chlorine, (C₁-C₄)-alkyl, methoxy, ethoxy and(C₃-C₅)-cycloalkyl, wherein said (C₁-C₄)-alkyl is optionally substitutedwith a group selected from methoxy, difluoromethoxy, trifluoromethoxy,—NR¹⁴R¹⁵, cyclopropyl or optionally with up to three fluorine atoms,wherein R¹⁴ is (C₁-C₄)-alkyl, R¹⁵ is (C₁-C₄)-alkyl, or R¹⁴ and R¹⁵together with the nitrogen atom they are attached form a 4- to6-membered heterocycle wherein said 4- to 6-membered heterocycle isoptionally substituted with methyl or trifluoromethyl or optionally withup to four fluorine atoms, wherein said methoxy and ethoxy areoptionally substituted with up to three fluorine atoms, wherein said(C₃-C₅)-cycloalkyl is optionally substituted with up to four fluorineatoms, R⁶ is pyridyl or (C₅-C₈)-cycloalkyl, or is a group of the formula

wherein ## is the point of attachment to the pyrazole ring, R³⁸ is ahydrogen atom, methyl or fluorine, R^(38a) is a hydrogen atom, R³⁹ is ahydrogen atom, cyano or fluorine, R^(39a) is a hydrogen atom, cyano,fluorine or methylsulfanyl, R⁴⁰ is a hydrogen atom, fluorine, chlorine,cyano, hydroxy, —(CH₂)_(n)NR¹⁶R¹⁷, methyl, methoxy, ethoxy,difluoromethoxy, trifluoromethoxy, methoxycarbonyl or ethoxycarbonyl,wherein said methyl is optionally substituted with cyano or optionallywith up to three fluorine atoms, wherein n is 0, R¹⁶ is a hydrogen atomor (C₁-C₄)-alkyl, R¹⁷ is (C₁-C₄)-alkyl, wherein said pyridyl isoptionally substituted, identically or differently, with one or twogroups selected from fluorine, cyano, methyl, methoxy and ethoxy,wherein said methyl is optionally substituted with up to three fluorineatoms, wherein said methoxy is optionally substituted with up to threefluorine atoms, wherein said (C₅-C₈)-cycloalkyl is optionallysubstituted, identically or differently, with one or two groups selectedfrom (C₁-C₄)-alkyl and cyano, or optionally with up to five fluorineatoms, wherein said (C₁-C₄)-alkyl is optionally substituted with up tothree fluorine atoms, R⁷ is a hydrogen atom or (C₁-C₄)-alkyl, whereinsaid (C₁-C₄)-alkyl is optionally substituted with (C₃-C₆)-cycloalkyl,methoxy or ethoxy or optionally with up to three fluorine atoms, withthe proviso that if R⁵ is methoxy, ethoxy, difluoromethoxy ortrifluoromethoxy then R⁷ is different from hydrogen, with the provisothat if R⁶ is pyridyl then R⁷ is different from hydrogen, R⁸ is a groupselected from chlorine, (C₁-C₄)-alkyl, methoxy, ethoxy and(C₃-C₅)-cycloalkyl, wherein said (C₁-C₄)-alkyl is optionally substitutedwith a group selected from methoxy —NR²²R²³, cyclopropyl or optionallywith up to three fluorine atoms, wherein said methoxy is optionallysubstituted with up to three fluorine atoms, wherein R²² is(C₁-C₄)-alkyl, R²³ is (C₁-C₄)-alkyl, wherein said methoxy and ethoxy areoptionally substituted with up to three fluorine atoms, and wherein said(C₃-C₅)-cycloalkyl is optionally substituted with up to four fluorineatoms, R⁹ is pyridyl or (C₅-C₈)-cycloalkyl, or is a group of the formula

wherein ## is the point of attachment to the pyrazole ring, R^(38b) is ahydrogen atom, methyl or fluorine, R^(38c) is a hydrogen atom orfluorine, R^(39b) is a hydrogen atom, cyano or fluorine, R^(39c) is ahydrogen atom, cyano or fluorine, R^(40a) is a hydrogen atom, fluorine,chlorine, cyano, hydroxy, —(CH₂)_(n)NR^(16a)R^(17a), methyl, methoxy,ethoxy, difluoromethoxy, trifluoromethoxy, methoxycarbonyl orethoxycarbonyl, a 4- to 6-membered heterocycle, cyclopropyl orcyclobutyl, wherein said methyl is optionally substituted with cyano oroptionally with up to three fluorine atoms, wherein n is 0, R^(16a) is ahydrogen atom, R^(17a) is (C₁-C₄)-alkyl, wherein said 4- to 6-memberedheterocycle is optionally substituted, with methyl or optionally with upto five fluorine atoms, wherein said pyridyl is optionally substituted,identically or differently, with one or two groups selected fromfluorine, cyano, methyl, methoxy and ethoxy, wherein said methyl isoptionally substituted with up to three fluorine atoms, wherein saidmethoxy and ethoxy are optionally substituted with up to three fluorineatoms, wherein said (C₅-C₈)-cycloalkyl is optionally substituted,identically or differently, with one or two groups selected from methyl,ethyl, cyano or optionally with up to five fluorine atoms, wherein saidmethyl is optionally substituted with up to three fluorine atoms, R¹⁰ isa hydrogen atom, (C₁-C₄)-alkyl or cyclopropyl, wherein said(C₁-C₄)-alkyl is optionally substituted with a group selected from(C₃-C₆)-cycloalkyl, methoxy, ethoxy, 2-methyl-2H-tetrazol-5-yl,1-methyl-1H-tetrazol-5-yl, -NR²⁸R²⁹ or optionally with up to threefluorine atoms and is optionally additionally substituted with hydroxy,wherein said (C₃-C₆)-cycloalkyl is optionally substituted with up tofour fluorine atoms, and wherein R²⁸ is a hydrogen atom or(C₁-C₄)-alkyl, R²⁹ is (C₁-C₄)-alkyl, with the proviso that if R⁹ ispyridyl then R¹⁰ is different from hydrogen, with the proviso that if R⁸is methoxy, ethoxy, difluoromethoxy or trifluoromethoxy then R¹⁹ isdifferent from hydrogen, R¹¹ is cyclopropyl, methyl or ethyl, whereinsaid methyl or ethyl are optionally substituted with cyclopropyl oroptionally with up to three fluorine atoms, R¹² is a group of theformula

wherein ## is the point of attachment to the pyrazole ring, R^(38d) is ahydrogen atom or fluorine, R^(38e) is a hydrogen atom, R^(39d) is ahydrogen atom or fluorine, R^(39e) is a hydrogen atom, R^(40b) is ahydrogen atom, fluorine, chlorine or cyano, R¹³ is a group selected froma hydrogen atom, methyl and cyclopropyl, wherein said methyl isoptionally substituted with cyclopropyl or optionally with up to threefluorine atoms, R² is a hydrogen atom or methyl, wherein said methyl isoptionally substituted with up to three fluorine atoms, R³ is a groupselected from a hydrogen atom, fluorine, chlorine, bromine, cyano,hydroxy, nitro, amino, mono-(C₁-C₄)-alkylamino, di-(C₁-C₄)-alkylamino,methylsulfanyl, ethylsulfanyl, methyl sulfinyl, ethyl sulfinyl, methylsulfonyl, ethyl sulfonyl, —O—C(═O)—OR^(37a), —NH—C(═O)—NR³⁶R³⁷,—N(CH₃)—C(═O)—NR³⁶R³⁷, —NH—C(═O)—OR^(37a), (C₁-C₄)-alkyl, methoxy,ethoxy, (C₃-C₅)-cycloalkyl, 4- to 6-membered heterocycle, 5-memberedheteroaryl, —(CH₂)_(q)—C(═O)—NR³⁴R³⁵, methoxycarbonyl andethoxycarbonyl, wherein said (C₁-C₄)-alkyl is optionally substituted,identically or differently, with one or two groups selected fromhydroxy, cyano, methoxy, ethoxy, methoxycarbonyl, ethoxycarbonyl,methylamino, ethylamino, dimethylamino, diethylamino, a 4- to 6-memberedheterocycle and cyclopropyl and optionally up to three fluorine atoms,wherein said 4- to 6-membered heterocycle is optionally substituted withmethyl, ethyl or cyclopropyl and optionally up to two fluorine atoms,wherein said methoxy and ethoxy are optionally substituted with cyano,cyclopropyl or optionally up to three fluorine atoms, wherein said(C₃-C₅)-cycloalkyl is optionally substituted with hydroxy or optionallywith up to four fluorine atoms, wherein said 4- to 6-memberedheterocycle is optionally substituted with hydroxyl or trifluoromethylor optionally with up to four fluorine atoms, wherein said 5-memberedheteroaryl is optionally substituted, identically or differently, withone or two groups selected from methyl and methoxy wherein q is 0, R³⁴is a hydrogen atom or (C₁-C₄)-alkyl, R³⁵ is (C₁-C₄)-alkyl, or R³⁴ andR³⁵ together with the nitrogen atom they are attached form a 4- to6-membered heterocycle ring wherein said 4- to 6-membered heterocyclering is optionally substituted, identically or differently, with one ortwo groups selected from a fluorine atom, methyl, difluoromethyl,trifluoromethyl and trifluoromethoxy, wherein R³⁶ is a hydrogen atom ormethyl, R³⁷ is a hydrogen atom, methyl, difluoromethyl, trifluoromethylor cyclopropyl, R^(37a) is methyl, difluoromethyl, trifluoromethyl orcyclopropyl, with the proviso that if R³ is —(CH₂)_(q)C(═O)—NR³⁴R³⁵,—O—C(═O)—OR^(37a), —NH—C(═O)—NR³⁶R³⁷, —N(CH₃)—C(═O)—NR³⁶R³⁷ or—NH—C(═O)—OR^(37a), then R⁷ and R¹⁰ are different from hydrogen, withthe proviso that if R³ is cyano then R² and R⁴ are different fromhydrogen, with the proviso that if R³ is cyano then R⁶ and R⁹ aredifferent from pyridyl or pyrimidyl, or R² and R³ together with thecarbon atoms they are attached form a 4- to 6-membered carbocycle, a 5-to 6-membered azaheterocycle, a 5- to 6-membered oxaheterocycle, a6-membered heteroaryl group or a phenyl ring, wherein said phenyl groupis optionally substituted, identically or differently, with one or twogroups selected from fluorine, chlorine, methyl, trifluoromethyl,methxoy and trifluoromethoxy, wherein said 5- to 6-membered carbocycleis optionally substituted, identically or differently, with one or twogroups selected from hydroxy, oxo, methyl, ethyl, trifluoromethyl and(C₁-C₄)-alkoxycarbonyl or optionally with up to four fluorine atoms,wherein said 5- to 6-membered azaheterocycle is optionally substitutedwith oxo, methyl, ethyl, propyl, trifluoromethyl, tert.-butoxycarbonylor optionally with up to four fluorine atoms, wherein said 5- to6-membered oxaheterocycle is optionally substituted with oxo, methyl,ethyl, trifluoromethyl, methoxycarbonyl and ethoxycarbonyl or optionallywith up to four fluorine atoms, with the proviso that if R² and R³together with the carbon atoms they are attached to form a 5- to6-membered azaheterocycle with a non-substituted nitrogen atom which isnot directly attached to the pyrazole, then R⁷ and R¹⁰ are differentfrom hydrogen, with the proviso that if R⁷ and R¹⁰ are hydrogen then thenitrogen atom of the 5- to 6-membered azaheterocycle formed by R² and R³together with the carbon atoms they are attached to is substituted withmethyl, ethyl, methoxycarbonyl or ethoxycarbonyl, R⁴ is a group selectedfrom a hydrogen atom, (C₁-C₄)-alkyl, cyclopropyl, methoxycarbonyl,ethoxycarbonyl and hydroxy, wherein said (C₁-C₄)-alkyl is optionallysubstituted with a group selected from hydroxy, methoxy and cyclopropylor optionally with up to three fluorine atoms, or R³ and R⁴ togetherwith the carbon atoms they are attached form a 5- to 6-memberedcarbocycle, a 5- to 6-membered heterocycle, a 6-membered heteroarylgroup or a phenyl ring, wherein said 5- to 6-membered heterocycle isoptionally substituted, identically or differently, with one or twogroups selected from oxo, methyl, ethyl, propyl, trifluoromethyl,methoxycarbonyl, ethoxycarbonyl, tert.-butoxycarbonyl or optionally withup to four fluorine atoms, wherein said 5- to 6-membered carbocycle isoptionally substituted, identically or differently, with one or twogroups selected from oxo, hydroxy, methyl, ethyl, trifluoromethylmethoxycarbonyl and ethoxycarbonyl or optionally with up to fourfluorine atoms, and wherein any phenyl group and any 6-memberedheteroaryl group are each optionally substituted, identically ordifferently, with one or two groups selected from fluorine, chlorine,methyl, ethyl, trifluoromethyl, methxoy and trifluoromethoxy, with theproviso that if R³ and R⁴ together with the carbon atoms they areattached form a 5- to 6-membered heterocycle with a non-substitutednitrogen atom which is not directly attached to the pyrazole, then R⁷and R¹⁰ is different from hydrogen, with the proviso that if R⁷ and R¹⁰are hydrogen then the nitrogen atom of the 5- to 6-membered heterocycleformed by R³ and R⁴ together with the carbon atoms they are attached tois substituted with methyl, ethyl, methoxycarbonyl or ethoxycarbonyl, ora stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or a saltthereof, or a mixture of same.
 28. The method of claim 25, wherein: R¹is a group of the formula

wherein # is the point of attachment to the amino group, R⁵ is a groupselected from chlorine, methyl, ethyl, methoxy or cyclopropyl, whereinsaid methyl and ethyl are optionally substituted with methoxy oroptionally with up to three fluorine atoms, wherein said methoxy isoptionally substituted with up to three fluorine atoms, R⁶ is5-fluoropyridin-2-yl, 6-trifluoromethylpyridin-3-yl or cyclohexyl, or isa group of the formula

wherein ## is the point of attachment to the pyrazole ring, R³⁸ is ahydrogen atom or fluorine, R^(38a) is a hydrogen atom, R³⁹ is a hydrogenatom, R^(39a) is a hydrogen atom or cyano, R⁴⁰ is a hydrogen atom,fluorine, chlorine, cyano, methyl, difluoromethyl, trifluoromethyl,methoxy, ethoxy, difluoromethoxy, trifluoromethoxy, methoxycarbonyl orethoxycarbonyl, R⁷ is a hydrogen atom, methyl, ethyl, cyclopropylmethyl,2-cyclopropylethyl or 2,2-difluoroethyl, with the proviso that if R⁵ ismethoxy, difluoromethoxy or trifluoromethoxy then R⁷ is different fromhydrogen, with the proviso that if R⁶ is 5-fluoropyridin-2-yl or6-trifluoromethylpyridin-3-yl then R⁷ is different from hydrogen, R⁸ isa group selected from chlorine, methyl, ethyl, methoxy and cylcopropyl,R⁹ is pyridyl or4-cyanopentacyclo[4.2.0.0^(2,5).0^(3,8).0^(4,7)]octan-1-yl, or is agroup of the formula

wherein ## is the point of attachment to the pyrazole ring, R^(38b) is ahydrogen atom or fluorine, R^(38c) is a hydrogen atom, R^(39b) is ahydrogen atom, R^(39c) is a hydrogen atom, R^(40a) is a hydrogen atom,fluorine, chlorine, cyano, methyl, difluoromethyl, trifluoromethyl,methylamino, methoxy, difluoromethoxy, trifluoromethoxy or cyclopropyl,wherein said pyridyl is optionally substituted with fluorine, methyl,difluoromethyl, trifluoromethyl or methoxy, R¹⁰ is a hydrogen atom,methyl, ethyl, 2,2-difluoroethyl, cyclopropylmethyl, cyclobutylmethyl,2-cyclopropylethyl, 2-cyclopropyl-2-hydroxypropyl,2-cyclopropyl-2-hydroxyethyl, 2-methoxyethyl, or cyclopropyl, whereinsaid methyl and ethyl are optionally substituted with a group selectedfrom cyclopropyl, methoxy or optionally up to three fluorine atoms andis optionally additionally substituted with hydroxy, with the provisothat if R⁹ is pyridyl then R¹⁰ is different from hydrogen, with theproviso that if R⁸ is methoxy then R¹⁰ is different from hydrogen, R¹¹is methyl, R¹² is a group of the formula

wherein ## is the point of attachment to the pyrazole ring, R^(38d) is ahydrogen atom, R^(38e) is a hydrogen atom, R^(39d) is a hydrogen atom,R^(39e) is a hydrogen atom, R^(40b) is fluorine or cyano, R¹³ is a groupselected from a hydrogen atom or methyl, R² is a hydrogen atom, methylor difluoromethyl, R³ is a group selected from a hydrogen atom,fluorine, chlorine, bromine, cyano, hydroxy, nitro, amino, ethylamino,dimethylamino , —O—C(═O)—NR³⁶R³⁷, —O—C(═O)—OR^(37a), —NH—C(═O)—OR^(37a),(C₁-C₄)-alkyl, methoxy, cyclopropyl, cyclobutyl, 4-membered heterocycle,1,3,4-oxadiazol-2-yl, 2-(trifluoromethyl)-1,3-dioxolan-2-yl,—(CH₂)_(q)—C(═O)—NR³⁴R³⁵, methoxycarbonyl and ethoxycarbonyl, whereinsaid (C₁-C₄)-alkyl is optionally substituted, identically ordifferently, with one or two groups selected from hydroxy, methoxy,methoxycarbonyl, ethoxycarbonyl, dimethylamino, a 4-memberedazaheterocycle and cyclopropyl and optionally up to three fluorineatoms, wherein said 4-membered azaheterocycle is optionally substitutedwith up to two fluorine atoms, wherein said methoxy is optionallysubstituted with cyano, cyclopropyl and optionally up to three fluorineatoms, wherein said cyclopropyl and cyclobutyl are optionallysubstituted with hydroxy, wherein said 4-membered heterocycle isoptionally substituted with hydroxy, wherein said 1,3,4-oxadiazol-2-ylis optionally substituted with methyl, wherein q is 0, R³⁴ is methyl,R³⁵ is methyl, or R³⁴ and R³⁵ together with the nitrogen atom they areattached form a 4- to 6-membered heterocycle ring wherein said 4- to6-membered heterocycle ring is optionally substituted, identically ordifferently, with one or two groups selected from a fluorine atom,methyl, difluoromethyl and trifluoromethyl, wherein R³⁶ is a methylatom, R³⁷ is a hydrogen atom or methyl, R^(37a) is methyl, with theproviso that if R³ is —(CH₂)_(q)C(═O)—NR³⁴R³⁵ O—C(═O)—NR³⁶R³⁷,—O—C(═O)—OR^(37a) or —NH—C(═O)—OR^(37a), then R⁷ and R¹⁰ are differentfrom hydrogen, with the proviso that if R³ is cyano then R² and R⁴ aredifferent from hydrogen, with the proviso that if R³ is cyano then R⁶and R⁹ are different from pyridyl, or R² and R³ together with the carbonatoms they are attached form a 5- to 6-membered carbocycle, apyrrolidinyl, a pyridyl or a phenyl ring, wherein said 5- to 6-memberedcarbocycle is optionally substituted, identically or differently, withone or two groups selected from oxo, methyl, trifluoromethyl andhydroxy, wherein said pyrrolidinyl is substituted with propyl ortert-butoxycarbonyl, R⁴ is a group selected from a hydrogen atom,methyl, 2-hydroxypropan-2-yl, fluoromethyl, difluoromethyl,methoxycarbonyl, ethoxycarbonyl and hydroxy, or R³ and R⁴ together withthe carbon atoms they are attached form a 5- to 6-membered carbocycle, apyrrolidinyl ring or a piperidinyl ring, a pyridyl group or a phenylring, wherein said pyrrolidinyl ring is substituted with propyl ortert-butoxycarbonyl, wherein said piperidinyl ring is substituted withpropyl or tert-butoxycarbonyl, wherein said 5- to 6-membered carbocycleis optionally substituted, identically or differently, with one or twogroups selected from oxo, hydroxy and methyl, or a stereoisomer, atautomer, an N-oxide, a hydrate, a solvate, or a salt thereof, or amixture of same.
 29. The method of claim 25, wherein the compound is

or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or asalt thereof, or a mixture of same.
 30. The method of claim 25, whereinthe compound is

or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or asalt thereof, or a mixture of same.
 31. The method of claim 25, whereinthe compound is

or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or asalt thereof, or a mixture of same.
 32. The method of claim 25, whereinthe compound is

or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or asalt thereof, or a mixture of same.
 33. The method of claim 25, whereinthe compound of formula (I), or a stereoisomer, a tautomer, an N-oxide,a hydrate, a solvate, or a salt thereof, or a mixture of same, isadministered as a pharmaceutical composition comprising the compound offormula (I), or a stereoisomer, a tautomer, an N-oxide, a hydrate, asolvate, or a salt thereof, or a mixture of same, in combination with aninert, non-toxic, pharmaceutically suitable auxiliary.
 34. The method ofclaim 25, wherein the compound of formula (I), or a stereoisomer, atautomer, an N-oxide, a hydrate, a solvate, or a salt thereof, or amixture of same, is administered as a pharmaceutical combinationcomprising the compound of formula (I), or a stereoisomer, a tautomer,an N-oxide, a hydrate, a solvate, or a salt thereof, or a mixture ofsame, in combination with a further active compound selected from thegroup consisting of the hypotensive active compounds, of theanti-inflammatory agents/immunosuppressive agents, the phosphatebinders, the sodium-phosphate co-transporters, NHE3 inhibitors,antiarrhythmic agents, agents that alter lipid metabolism and the activecompounds which modulate vitamin D metabolism.